Published in Am J Hum Genet on August 01, 1995
Pax9-deficient mice lack pharyngeal pouch derivatives and teeth and exhibit craniofacial and limb abnormalities. Genes Dev (1998) 3.49
Complete sequencing shows a role for MSX1 in non-syndromic cleft lip and palate. J Med Genet (2003) 2.72
Mice devoid of gamma-aminobutyrate type A receptor beta3 subunit have epilepsy, cleft palate, and hypersensitive behavior. Proc Natl Acad Sci U S A (1997) 2.16
p63 Gene mutations in eec syndrome, limb-mammary syndrome, and isolated split hand-split foot malformation suggest a genotype-phenotype correlation. Am J Hum Genet (2001) 2.02
Association of MSX1 and TGFB3 with nonsyndromic clefting in humans. Am J Hum Genet (1998) 1.89
Genome scan for loci involved in cleft lip with or without cleft palate, in Chinese multiplex families. Am J Hum Genet (2002) 1.44
Genetic Factors and Orofacial Clefting. Semin Orthod (2008) 1.05
Rehabilitative treatment of cleft lip and palate: experience of the Hospital for Rehabilitation of Craniofacial Anomalies/USP (HRAC/USP)--Part 1: overall aspects. J Appl Oral Sci (2012) 1.03
Current concepts in genetics of nonsyndromic clefts. Indian J Plast Surg (2009) 0.98
Genome scan for teratogen-induced clefting susceptibility loci in the mouse: evidence of both allelic and locus heterogeneity distinguishing cleft lip and cleft palate. Proc Natl Acad Sci U S A (1997) 0.96
Maternal factors and disparities associated with oral clefts. Ethn Dis (2010) 0.91
Nonsyndromic cleft lip with or without cleft palate: new BCL3 information. Am J Hum Genet (1996) 0.89
Linkage analysis in a large Brazilian family with van der Woude syndrome suggests the existence of a susceptibility locus for cleft palate at 17p11.2-11.1. Am J Hum Genet (1999) 0.87
Genetics of cleft lip and palate : a review. Malays J Med Sci (2007) 0.82
TGFA and IRF6 contribute to the risk of nonsyndromic cleft lip with or without cleft palate in northeast China. PLoS One (2013) 0.81
Evidence for transforming growth factor-beta 3 gene polymorphism in non-syndromic cleft lip and palate patients from Indian sub-continent. Med Oral Patol Oral Cir Bucal (2012) 0.80
Panel perception of facial appearance of cleft patients generated by use of a morphing technique. Oral Maxillofac Surg (2014) 0.78
Autosomal dominant nonsyndromic cleft lip and palate: significant evidence of linkage at 18q21.1. Am J Hum Genet (2007) 0.78
Pathways and networks-based analysis of candidate genes associated with nicotine addiction. PLoS One (2015) 0.77
Comparison of periodontal status among patients with cleft lip, cleft palate, and cleft lip along with a cleft in palate and alveolus. J Indian Soc Periodontol (2010) 0.77
Identification of a novel heterozygous truncation mutation in exon 1 of ARHGAP29 in an Indian subject with nonsyndromic cleft lip with cleft palate. Eur J Dent (2014) 0.76
The genetic basis of facial skeletal characteristics and its relation with orthodontics. Eur J Dent (2012) 0.75
Cleft palate repair in Mongolia: Modified palatoplasty vs. conventional technique. Ann Maxillofac Surg (2012) 0.75
Analysis of microsatellite polymorphisms in South Indian patients with non syndromic cleft lip and palate. Balkan J Med Genet (2013) 0.75
Genetic dissection of complex traits. Science (1994) 29.54
Hox genes in vertebrate development. Cell (1994) 9.27
Pattern of malformation in offspring of chronic alcoholic mothers. Lancet (1973) 7.45
Retinoic acid embryopathy. N Engl J Med (1985) 5.85
The diastrophic dysplasia gene encodes a novel sulfate transporter: positional cloning by fine-structure linkage disequilibrium mapping. Cell (1994) 5.21
Msx1 deficient mice exhibit cleft palate and abnormalities of craniofacial and tooth development. Nat Genet (1994) 5.19
Elevated blood pressure and craniofacial abnormalities in mice deficient in endothelin-1. Nature (1994) 5.00
Regionally restricted developmental defects resulting from targeted disruption of the mouse homeobox gene hox-1.5. Nature (1991) 4.60
Association of genetic variation of the transforming growth factor-alpha gene with cleft lip and palate. Am J Hum Genet (1989) 4.13
TGF alpha deficiency results in hair follicle and eye abnormalities in targeted and waved-1 mice. Cell (1993) 4.02
Deletions and microdeletions of 22q11.2 in velo-cardio-facial syndrome. Am J Med Genet (1992) 3.74
Immunohistologic abnormalities of the microfibrillar-fiber system in the Marfan syndrome. N Engl J Med (1990) 3.63
Waardenburg's syndrome patients have mutations in the human homologue of the Pax-3 paired box gene. Nature (1992) 3.63
Positional cloning moves from perditional to traditional. Nat Genet (1995) 3.37
Suggestion of linkage of a major locus for nonsyndromic orofacial cleft with F13A and tentative assignment to chromosome 6. Clin Genet (1987) 3.14
The genetics of cleft lip and cleft palate. Am J Hum Genet (1970) 2.94
Developmental defects of the ear, cranial nerves and hindbrain resulting from targeted disruption of the mouse homeobox gene Hox-1.6. Nature (1992) 2.82
Palate development. Development (1988) 2.80
High postnatal lethality and testis degeneration in retinoic acid receptor alpha mutant mice. Proc Natl Acad Sci U S A (1993) 2.78
Maternal rescue of transforming growth factor-beta 1 null mice. Science (1994) 2.28
Segregation analysis of cleft lip with or without cleft palate: a comparison of Danish and Japanese data. Am J Hum Genet (1986) 2.23
Nonsyndromic cleft lip with or without cleft palate: evidence of linkage to BCL3 in 17 multigenerational families. Am J Hum Genet (1995) 2.12
Cleft lip with or without cleft palate: associations with transforming growth factor alpha and retinoic acid receptor loci. Am J Hum Genet (1992) 2.12
Complex segregation analysis of nonsyndromic cleft lip and palate. Am J Hum Genet (1991) 2.01
Further evidence for an association between genetic variation in transforming growth factor alpha and cleft lip and palate. Am J Hum Genet (1991) 1.98
Cleft lip and palate: no evidence of linkage to transforming growth factor alpha. Am J Hum Genet (1991) 1.94
Functional inhibition of retinoic acid response by dominant negative retinoic acid receptor mutants. Proc Natl Acad Sci U S A (1993) 1.81
Evidence of a locus for orofacial clefting on human chromosome 6p24 and STS content map of the region. Hum Mol Genet (1995) 1.75
Mice with targeted disruptions in the paralogous genes hoxa-3 and hoxd-3 reveal synergistic interactions. Nature (1994) 1.66
Mode of inheritance of nonsyndromic cleft lip with or without cleft palate: a reanalysis. Am J Hum Genet (1992) 1.66
Familial recurrence-pattern analysis of cleft lip with or without cleft palate. Am J Hum Genet (1992) 1.64
Association study of transforming growth factor alpha (TGF alpha) TaqI polymorphism and oral clefts: indication of gene-environment interaction in a population-based sample of infants with birth defects. Am J Epidemiol (1995) 1.62
Etiology of facial clefts: prospective evaluation of 428 patients. Cleft Palate J (1988) 1.61
Linkage analysis versus association analysis: distinguishing between two models that explain disease-marker associations. Am J Hum Genet (1993) 1.61
Linkage of an autosomal dominant clefting syndrome (Van der Woude) to loci on chromosome Iq. Am J Hum Genet (1990) 1.48
Exclusion of candidate genes from a role in cleft lip with or without cleft palate: linkage and association studies. J Med Genet (1993) 1.45
Linkage of a human brain malformation, familial holoprosencephaly, to chromosome 7 and evidence for genetic heterogeneity. Proc Natl Acad Sci U S A (1994) 1.43
Linkage of an X-chromosome cleft palate gene. Nature (1987) 1.42
Cleft lip with or without cleft palate in Shanghai, China: evidence for an autosomal major locus. Am J Hum Genet (1992) 1.38
Genetic analysis in families with van der Woude syndrome. J Craniofac Genet Dev Biol (1985) 1.37
Periconceptional supplementation with vitamins and folic acid to prevent recurrence of cleft lip. Lancet (1982) 1.30
Confirmation of an association between RFLPs at the transforming growth factor-alpha locus and non-syndromic cleft lip and palate. J Med Genet (1992) 1.28
Association of transforming growth-factor alpha gene polymorphisms with nonsyndromic cleft palate only (CPO). Am J Hum Genet (1993) 1.27
Nonsyndromic cleft lip and palate: no evidence of linkage to HLA or factor 13A. Am J Hum Genet (1993) 1.23
Does maternal cigarette smoking during pregnancy cause cleft lip and palate in offspring? Am J Dis Child (1989) 1.20
A cluster of three GABAA receptor subunit genes is deleted in a neurological mutant of the mouse p locus. Nature (1993) 1.19
Expression of the murine Dlx-1 homeobox gene during facial, ocular and limb development. Differentiation (1992) 1.16
Experimental fetal alcohol syndrome: proposed pathogenic basis for a variety of associated facial and brain anomalies. Am J Med Genet (1992) 1.15
Genetic and physical mapping of the Treacher Collins syndrome locus: refinement of the localization to chromosome 5q32-33.2. Hum Mol Genet (1992) 1.15
Retinoic acid-induced alterations in the expression of growth factors in embryonic mouse palatal shelves. Teratology (1990) 1.13
No evidence of linkage between the transforming growth factor-alpha gene in families with apparently autosomal dominant inheritance of cleft lip and palate. J Med Genet (1992) 1.12
Genetic variation in transforming growth factor alpha: possible association of BamHI polymorphism with bilateral sporadic cleft lip and palate. Am J Hum Genet (1992) 1.09
Selection bias in genetic-epidemiological studies of cleft lip and palate. Am J Hum Genet (1992) 1.09
Association between alleles of the transforming growth factor-alpha locus and the occurrence of cleft lip. Am J Med Genet (1993) 1.04
Resolving an apparent paradox concerning the role of TGFA in CL/P. Am J Hum Genet (1993) 1.00
Nonsyndromic cleft lip and palate: evidence of linkage to a microsatellite marker on 6p23. Am J Hum Genet (1995) 0.98
Possible localization of a major gene for cleft lip and palate to 4q. Clin Genet (1994) 0.98
Cleft lip (+/- cleft palate) etiology: a search for solutions. Am J Med Genet (1992) 0.97
Maternal cigarette smoking during pregnancy in relation to oral clefts. Am J Epidemiol (1990) 0.95
Inhibition of neural crest cell attachment by integrin antisense oligonucleotides. Science (1993) 0.93
Immunolocalization of epidermal growth factor (EGF), EGF receptor and transforming growth factor alpha (TGF alpha) during murine palatogenesis in vivo and in vitro. Anat Embryol (Berl) (1991) 0.93
The major locus for multifactorial nonsyndromic cleft lip maps to mouse chromosome 11. Mamm Genome (1995) 0.91
Further evidence of a relationship between the retinoic acid receptor alpha locus and nonsyndromic cleft lip with or without cleft palate (CL +/- P) Am J Hum Genet (1993) 0.87
Evidence, from family studies, for linkage disequilibrium between TGFA and a gene for nonsyndromic cleft lip with or without cleft palate. Am J Hum Genet (1994) 0.87
An autosomal dominant mutation of facial development in a transgenic mouse. Dev Genet (1988) 0.85
Van der Woude syndrome and nonsyndromic cleft lip and palate. Am J Hum Genet (1992) 0.83
Pathogenesis of cleft palate in Treacher Collins, Nager, and Miller syndromes. Cleft Palate J (1989) 0.83
Evidence for an association between RFLPs at the transforming growth factor alpha (locus) and nonsyndromic cleft lip/palate in a South American population. Am J Hum Genet (1995) 0.83
Exclusion of retinoic acid receptor and a cartilage matrix protein in non-syndromic CL(P) families. J Med Genet (1995) 0.83
Restriction fragment length polymorphisms, glucocorticoid receptors, and phenytoin-induced cleft palate in congenic strains of mice with steroid susceptibility differences. J Craniofac Genet Dev Biol (1992) 0.78
A region of the mouse genome homologous to human chromosome 1q21 affects facial clefting. J Craniofac Genet Dev Biol (1993) 0.78
Transforming growth factor alpha: a modifying locus for nonsyndromic cleft lip with or without cleft palate? Eur J Hum Genet (1994) 0.77
Vitamin A-enhanced cleft palate susceptibility gene maps between C4 and B144 within the H-2 complex. Proc Soc Exp Biol Med (1993) 0.77
Comprehensive human genetic maps: individual and sex-specific variation in recombination. Am J Hum Genet (1998) 19.35
Long-circulating and target-specific nanoparticles: theory to practice. Pharmacol Rev (2001) 10.02
Cloning and characterization of a novel bicoid-related homeobox transcription factor gene, RIEG, involved in Rieger syndrome. Nat Genet (1996) 4.21
Association of genetic variation of the transforming growth factor-alpha gene with cleft lip and palate. Am J Hum Genet (1989) 4.13
RFLPs for transforming growth factor alpha (TGFA) gene at 2p13. Nucleic Acids Res (1986) 3.72
A collection of tri- and tetranucleotide repeat markers used to generate high quality, high resolution human genome-wide linkage maps. Hum Mol Genet (1995) 3.44
Integrated human genome-wide maps constructed using the CEPH reference panel. Nat Genet (1994) 3.06
A novel homeobox gene PITX3 is mutated in families with autosomal-dominant cataracts and ASMD. Nat Genet (1998) 2.82
Complete sequencing shows a role for MSX1 in non-syndromic cleft lip and palate. J Med Genet (2003) 2.72
Polymorphic human glucose transporter gene (GLUT) is on chromosome 1p31.3----p35. Diabetes (1987) 2.72
Changing character of cervical cancer in young women. BMJ (1989) 2.66
Linkage disequilibrium and evolutionary relationships of DNA variants (restriction enzyme fragment length polymorphisms) at the serum albumin locus. Proc Natl Acad Sci U S A (1984) 2.64
MSX1, PAX9, and TGFA contribute to tooth agenesis in humans. J Dent Res (2004) 2.26
The many faces and factors of orofacial clefts. Hum Mol Genet (1999) 2.16
The CEPH consortium linkage map of human chromosome 1. Genomics (1991) 2.09
Genome-wide association scan for childhood caries implicates novel genes. J Dent Res (2011) 2.05
Domain-specific mutations in TGFB1 result in Camurati-Engelmann disease. Nat Genet (2000) 2.02
Pitx2, a bicoid-type homeobox gene, is involved in a lefty-signaling pathway in determination of left-right asymmetry. Cell (1998) 1.93
Molecular genetics of human serum albumin: restriction enzyme fragment length polymorphisms and analbuminemia. Proc Natl Acad Sci U S A (1983) 1.89
Association of MSX1 and TGFB3 with nonsyndromic clefting in humans. Am J Hum Genet (1998) 1.89
Epidermal cells adhere preferentially to type IV (basement membrane) collagen. J Cell Biol (1979) 1.86
Orofacial clefts, parental cigarette smoking, and transforming growth factor-alpha gene variants. Am J Hum Genet (1996) 1.71
Mutations in the human forkhead transcription factor FOXE3 associated with anterior segment ocular dysgenesis and cataracts. Hum Mol Genet (2001) 1.66
The DNA rearrangement associated with facioscapulohumeral muscular dystrophy involves a heterochromatin-associated repetitive element: implications for a role of chromatin structure in the pathogenesis of the disease. Chromosome Res (1994) 1.63
RFLPs for epidermal growth factor (EGF), a single copy sequence at 4q25-4q27. Nucleic Acids Res (1986) 1.62
Rapid RFLP screening procedure identifies new polymorphisms at albumin and alcohol dehydrogenase loci. Hum Genet (1987) 1.58
The Pitx2 protein in mouse development. Dev Dyn (2000) 1.55
Changes in cartilage composition and physical properties due to stromelysin degradation. Arthritis Rheum (1995) 1.52
Dandy-Walker malformation: etiologic heterogeneity and empiric recurrence risks. Clin Genet (1985) 1.52
Antagonistic signals between BMP4 and FGF8 define the expression of Pitx1 and Pitx2 in mouse tooth-forming anlage. Dev Biol (2000) 1.52
Localization of dominantly inherited isolated triphalangeal thumb to chromosomal region 7q36. J Orthop Res (2000) 1.47
Isolation of a new homeobox gene belonging to the Pitx/Rieg family: expression during lens development and mapping to the aphakia region on mouse chromosome 19. Hum Mol Genet (1997) 1.45
Linkage disequilibrium of plasminogen polymorphisms and assignment of the gene to human chromosome 6q26-6q27. Am J Hum Genet (1987) 1.43
PI(3) kinase is associated with a mechanism of immunoresistance in breast and prostate cancer. Oncogene (2008) 1.41
Identification of novel candidate genes associated with cleft lip and palate using array comparative genomic hybridisation. J Med Genet (2007) 1.40
Maternal and fetal variation in genes of cholesterol metabolism is associated with preterm delivery. J Perinatol (2007) 1.36
Loss of heterozygosity suggests tumor suppressor gene responsible for primary hepatocellular carcinoma. Proc Natl Acad Sci U S A (1989) 1.34
Folic acid and orofacial clefts: a review of the evidence. Oral Dis (2010) 1.33
Analysis of the p63 gene in classical EEC syndrome, related syndromes, and non-syndromic orofacial clefts. J Med Genet (2002) 1.33
A novel mutation in the PHF8 gene is associated with X-linked mental retardation with cleft lip/cleft palate. Clin Genet (2007) 1.32
Report of the committee on the genetic constitution of chromosome 4. Cytogenet Cell Genet (1989) 1.31
A HindIII RFLP demonstrated for the kit oncogene on chromosome 4. Nucleic Acids Res (1988) 1.31
TBX22 mutations are a frequent cause of cleft palate. J Med Genet (2004) 1.30
Studies of the candidate genes TGFB2, MSX1, TGFA, and TGFB3 in the etiology of cleft lip and palate in the Philippines. Cleft Palate Craniofac J (1997) 1.30
Confirming genes influencing risk to cleft lip with/without cleft palate in a case-parent trio study. Hum Genet (2013) 1.28
MSX1 and TGFB3 contribute to clefting in South America. J Dent Res (2003) 1.28
Microdeletions at chromosome bands 1q32-q41 as a cause of Van der Woude syndrome. Am J Med Genet (1999) 1.27
Association of transforming growth-factor alpha gene polymorphisms with nonsyndromic cleft palate only (CPO). Am J Hum Genet (1993) 1.27
Connective tissue structure: cell binding to collagen. J Invest Dermatol (1978) 1.26
A single-gene explanation for the probability of having idiopathic talipes equinovarus. Am J Hum Genet (1993) 1.26
A preliminary gene map for the Van der Woude syndrome critical region derived from 900 kb of genomic sequence at 1q32-q41. Genome Res (2000) 1.26
Deletion in the promoter region and altered expression of Pitx3 homeobox gene in aphakia mice. Hum Mol Genet (2000) 1.25
Characterization of a novel gene disrupted by a balanced chromosomal translocation t(2;19)(q11.2;q13.3) in a family with cleft lip and palate. Genomics (1998) 1.24
Targeted scan of fifteen regions for nonsyndromic cleft lip and palate in Filipino families. Am J Med Genet A (2004) 1.24
Linkage localization of Börjeson-Forssman-Lehmann syndrome. Am J Med Genet (1989) 1.23
Identification of a dominant negative homeodomain mutation in Rieger syndrome. J Biol Chem (2001) 1.21
RFLP for the glucocorticoid receptor (GRL) located at 5q11-5q13. Nucleic Acids Res (1987) 1.20
Antagonistic regulation of Dlx2 expression by PITX2 and Msx2: implications for tooth development. Gene Expr (2001) 1.18
Autosomal dominant iris hypoplasia is caused by a mutation in the Rieger syndrome (RIEG/PITX2) gene. Am J Ophthalmol (1998) 1.17
Chromosomal assignment of 2900 tri- and tetranucleotide repeat markers using NIGMS somatic cell hybrid panel 2. Genomics (1996) 1.16
PITX2 regulates procollagen lysyl hydroxylase (PLOD) gene expression: implications for the pathology of Rieger syndrome. J Cell Biol (2001) 1.16
Contributions of PTCH gene variants to isolated cleft lip and palate. Cleft Palate Craniofac J (2006) 1.16
Two novel frameshift mutations in NKX2.5 result in novel features including visceral inversus and sinus venosus type ASD. J Med Genet (2002) 1.14
Human microvessel endothelial cells: isolation, culture and characterization. In Vitro Cell Dev Biol Anim (1993) 1.14
Multiple RFLPs demonstrated for epidermal growth factor receptor (EGFR) on chromosome 7. Nucleic Acids Res (1987) 1.11
Minute supernumerary ring chromosome 22 associated with cat eye syndrome: further delineation of the critical region. Am J Hum Genet (1995) 1.10
Keloids: a review. J Am Acad Dermatol (1981) 1.10
Genetic susceptibility to preeclampsia: roles of cytosineto-thymine substitution at nucleotide 677 of the gene for methylenetetrahydrofolate reductase, 68-base pair insertion at nucleotide 844 of the gene for cystathionine beta-synthase, and factor V Leiden mutation. Am J Obstet Gynecol (2001) 1.10
The effect of follow-up on limiting non-participation bias in genetic epidemiologic investigations. Eur J Epidemiol (1998) 1.10
Genetic and physical maps of human chromosome 4 based on dinucleotide repeats. Genomics (1992) 1.09
A polypeptide factor produced by fibrosarcoma cells that induces endothelial tissue factor and enhances the procoagulant response to tumor necrosis factor/cachectin. J Biol Chem (1990) 1.09
The epidermal cell which selectively adheres to a collagen substrate is the basal cell. J Invest Dermatol (1980) 1.08
HincII and KpnI RFLPs for laminin B1 (LAMB1) gene on chromosome 7. Nucleic Acids Res (1988) 1.08
Adhesion characteristics of murine metastatic and nonmetastatic tumor cells in vitro. Cancer Res (1980) 1.07
Combination chemotherapy followed by surgery or radiotherapy in patients with locally advanced cervical cancer. Br J Obstet Gynaecol (1987) 1.07
Prostate adenocarcinoma cells release the novel proinflammatory polypeptide EMAP-II in response to stress. Cancer Res (2000) 1.06
Localization of the achondroplasia gene to the distal 2.5 Mb of human chromosome 4p. Hum Mol Genet (1994) 1.05
Maternal alcohol use and risk of orofacial cleft birth defects. Teratology (1996) 1.04
Genetic linkage map of facioscapulohumeral muscular dystrophy and five polymorphic loci on chromosome 4q35-qter. Am J Hum Genet (1992) 1.04
Regional assignment of the gene for human liver/bone/kidney alkaline phosphatase to chromosome 1p36.1-p34. Genomics (1988) 1.03
Evaluation of two putative susceptibility loci for oral clefts in the Danish population. Am J Epidemiol (2001) 1.02
Oral clefts, transforming growth factor alpha gene variants, and maternal smoking: a population-based case-control study in Denmark, 1991-1994. Am J Epidemiol (1999) 1.01
Angiogenesis is associated with vascular endothelial growth factor expression in cervical intraepithelial neoplasia. Br J Cancer (1997) 1.01
The effects of melphalan and misonidazole on the vasculature of a murine sarcoma. Br J Cancer (1987) 1.01
Characterization of the human HOX 7 cDNA and identification of polymorphic markers. Hum Mol Genet (1992) 1.01
Phylogenetic conservation and physical mapping of members of the H6 homeobox gene family. Mamm Genome (1995) 1.01
Resolving an apparent paradox concerning the role of TGFA in CL/P. Am J Hum Genet (1993) 1.00
Global oral health inequalities: challenges in the prevention and management of orofacial clefts and potential solutions. Adv Dent Res (2011) 1.00
A detailed multipoint gene map of chromosome 1q. Genomics (1990) 1.00
Coexpression of flt-1, flt-4 and KDR in freshly isolated and cultured human endothelial cells. Biochem Biophys Res Commun (1996) 0.99
Genetic associations of surfactant protein D and angiotensin-converting enzyme with lung disease in preterm neonates. J Perinatol (2011) 0.99
Rh isoimmunization related to amniocentesis. Am J Med Genet (1983) 0.99
Genetic studies in the Nigerian population implicate an MSX1 mutation in complex oral facial clefting disorders. Cleft Palate Craniofac J (2011) 0.98
Cloning, characterization, and mapping of the mouse homeobox gene Hmx1. Genomics (1998) 0.98
Survey of trinucleotide repeats in the human genome: assessment of their utility as genetic markers. Hum Mol Genet (1995) 0.98
Genetic evidence for the role of loci at 19q13 in cleft lip and palate. J Med Genet (2006) 0.98
Phenotypic and pathologic evaluation of the myd mouse. A candidate model for facioscapulohumeral dystrophy. J Neuropathol Exp Neurol (1995) 0.97
Isolation and characterization of a novel human paired-like homeodomain-containing transcription factor gene, VSX1, expressed in ocular tissues. Genomics (2000) 0.97
Analysis of select folate pathway genes, PAX3, and human T in a Midwestern neural tube defect population. Teratology (1999) 0.97