Published in J Craniofac Genet Dev Biol on January 01, 1990
Survival and recurrence after concomitant chemotherapy and radiotherapy for cancer of the uterine cervix: a systematic review and meta-analysis. Lancet (2001) 5.71
Usefulness of letters from hospitals to general practitioners. Br Med J (Clin Res Ed) (1984) 4.01
Variability in automatic activation as an unobtrusive measure of racial attitudes: a bona fide pipeline? J Pers Soc Psychol (1995) 3.14
Suggestion of linkage of a major locus for nonsyndromic orofacial cleft with F13A and tentative assignment to chromosome 6. Clin Genet (1987) 3.14
Salivary and pancreatic amylase: electrophoretic characterizations and genetic studies. Am J Hum Genet (1973) 3.12
Subclavian artery supply disruption sequence: hypothesis of a vascular etiology for Poland, Klippel-Feil, and Möbius anomalies. Am J Med Genet (1986) 2.95
Internal deletion in a collagen gene in a perinatal lethal form of osteogenesis imperfecta. Nature (1983) 2.73
Cleft lip+/-cleft palate: an overview of the literature and an analysis of Danish cases born between 1941 and 1968. Am J Med Genet (1980) 2.51
V(D)J recombination activates a p53-dependent DNA damage checkpoint in scid lymphocyte precursors. Genes Dev (1996) 2.29
Segregation analysis of cleft lip with or without cleft palate: a comparison of Danish and Japanese data. Am J Hum Genet (1986) 2.23
Evidence against either a premature stop codon or the absence of obese gene mRNA in human obesity. J Clin Invest (1995) 2.20
A proposed classification for heritable human dentine defects with a description of a new entity. Arch Oral Biol (1973) 2.16
Wiedemann-Beckwith syndrome: presentation of clinical and cytogenetic data on 22 new cases and review of the literature. Hum Genet (1986) 2.07
Hematologic neoplasia in patients treated for Hodgkin's disease. N Engl J Med (1977) 1.93
Improved outcome in Pierre Robin sequence: effect of multidisciplinary evaluation and management. Pediatrics (1990) 1.92
Genetic determinants of bone mass in adult women: a reevaluation of the twin model and the potential importance of gene interaction on heritability estimates. J Bone Miner Res (1991) 1.82
Histopathology in the prediction of relapse of patients with stage I testicular teratoma treated by orchidectomy alone. Lancet (1987) 1.79
The VATER association. Analysis of 46 patients. Am J Dis Child (1986) 1.78
Familial variation of head size and adjustment for parental head circumference. J Pediatr (1980) 1.76
A new overgrowth syndrome with accelerated skeletal maturation, unusual facies, and camptodactyly. J Pediatr (1974) 1.73
Synthesis and processing of a type I procollagen containing shortened pro-alpha 1(I) chains by fibroblasts from a patient with osteogenesis imperfecta. J Biol Chem (1983) 1.71
Multiple pterygium syndrome. Am J Dis Child (1978) 1.71
Multiexon deletion in an osteogenesis imperfecta variant with increased type III collagen mRNA. J Biol Chem (1985) 1.67
Monitoring mRNA decapping activity. Methods (1999) 1.64
The ectrodactyly-ectodermal dysplasia-clefting (EEC) syndrome. Report of 2 cases and review of the literature. Clin Genet (1972) 1.63
Evaluation of dietary influences on Escherichia coli O157:H7 shedding by sheep. Appl Environ Microbiol (1997) 1.60
Carboplatin or cisplatin? Lancet (1988) 1.53
Congenital contractural arachnodactyly. Report of four additional families and review of literature. Clin Genet (1985) 1.52
Cisplatin combination chemotherapy versus chlorambucil in advanced ovarian carcinoma: mature results of a randomized trial. J Clin Oncol (1985) 1.51
Attitude accessibility as a moderator of the attitude-perception and attitude-behavior relations: an investigation of the 1984 presidential election. J Pers Soc Psychol (1986) 1.51
The neurofibromatosis-Noonan syndrome. Am J Med Genet (1985) 1.49
49,XXXXY: a distinct phenotype. Three new cases and review. J Med Genet (1998) 1.43
Effect of cattle diet on Escherichia coli O157:H7 acid resistance. Appl Environ Microbiol (1999) 1.42
Bilateral testicular germ cell tumours: an increasing incidence and prevention by chemotherapy. Br J Urol (1988) 1.42
Developing new drugs for cancer. BMJ (1991) 1.39
Genetic analysis in families with van der Woude syndrome. J Craniofac Genet Dev Biol (1985) 1.37
Human salivary amylase: genetics of electrophoretic variants. Am J Hum Genet (1971) 1.33
First-stage autosomal genome screen in extended pedigrees suggests genes predisposing to low bone mineral density on chromosomes 1p, 2p and 4q. Eur J Hum Genet (1998) 1.32
Congenital X-linked cataract, dental anomalies and brachymetacarpalia. Birth Defects Orig Artic Ser (1974) 1.30
Trapezoidocephaly, midfacial hypoplasia and cartilage abnormalities with multiple synostoses and skeletal fractures. Birth Defects Orig Artic Ser (1975) 1.29
Incidence of cleft lip and palate in the offspring of cleft parents. Clin Genet (1971) 1.29
A randomised trial of cisplatin and vindesine versus supportive care only in advanced non-small cell lung cancer. Br J Cancer (1990) 1.28
Familial branchio-oto-renal dysplasia: a new addition to the branchial arch syndromes. Clin Genet (1976) 1.28
Simplified method for collection of pure submandibular saliva in large volumes. J Dent Res (1968) 1.28
The Nance-Horan syndrome: a rare X-linked ocular-dental trait with expression in heterozygous females. Clin Genet (1984) 1.27
Urorectal septum malformation sequence. Report of six cases and embryological analysis. Am J Dis Child (1987) 1.26
Cis-platinum: a new anticancer agent. Br Med J (1979) 1.24
Mutations in VPS16 and MRT1 stabilize mRNAs by activating an inhibitor of the decapping enzyme. Mol Cell Biol (1999) 1.23
Epileptic seizures associated with cisplatin administration. Cancer Treat Rep (1982) 1.22
A randomized comparison of tamoxifen with surgical oophorectomy in premenopausal patients with advanced breast cancer. J Clin Oncol (1986) 1.22
In utero brain destruction resulting in collapse of the fetal skull, microcephaly, scalp rugae, and neurologic impairment: the fetal brain disruption sequence. Am J Med Genet (1984) 1.21
Phenotypic variation in the popliteal pterygium syndrome. Clin Genet (1973) 1.21
Rescue of T cell-specific V(D)J recombination in SCID mice by DNA-damaging agents. Science (1994) 1.20
Cleft palate: a genetic and epidemiologic investigation. Clin Genet (1981) 1.20
Long-term bone loss in men: effects of genetic and environmental factors. Ann Intern Med (1992) 1.19
The acrocephalosyndactyly syndromes: a metacarpophalangeal pattern profile analysis. Clin Genet (1977) 1.18
Genetic linkage of familial granulomatous inflammatory arthritis, skin rash, and uveitis to chromosome 16. Am J Hum Genet (1996) 1.16
Radical radiotherapy for stage I/II non-small cell lung cancer in patients not sufficiently fit for or declining surgery (medically inoperable): a systematic review. Thorax (2001) 1.16
On the classification of the acrocephalosyndactyly syndromes. Clin Genet (1977) 1.15
The axial mesodermal dysplasia spectrum. Pediatrics (1981) 1.14
Interstitial deletion of the long arm of chromosome no. 7 (7q-) in an infant with multiple anomalies. Clin Genet (1976) 1.14
Phenotypic and genetic analysis of the silver-Russell syndrome. Clin Genet (1978) 1.11
Terminal and interstitial deletions of the long arm of chromosome 7: a review with five new cases. Am J Med Genet (1984) 1.11
Ruminant gastrointestinal cell proliferation and clearance of Escherichia coli O157:H7. Infect Immun (2000) 1.10
The hypothalamic leptin receptor in humans: identification of incidental sequence polymorphisms and absence of the db/db mouse and fa/fa rat mutations. Diabetes (1996) 1.09
Diagnostic criteria for the whistling face syndrome. Birth Defects Orig Artic Ser (1975) 1.09
A comparison of two doses of tamoxifen (Nolvadex) in postmenopausal women with advanced breast cancer: 10 mg bd versus 20 mg bd. Br J Cancer (1984) 1.08
Hypertelorism, microtia, and facial clefting. A newly described inherited syndrome. Am J Dis Child (1969) 1.07
Concerns about the genetics of pre-eclampsia. Am J Hum Genet (1993) 1.07
Periodontosis: a phenotypic and genetic analysis. Oral Surg Oral Med Oral Pathol (1976) 1.07
Fetal tissue derived from spontaneous pregnancy losses is insufficient for human transplantation. Obstet Gynecol (1995) 1.07
Mild autosomal dominant hypophosphatasia: in utero presentation in two families. Am J Med Genet (1999) 1.06
Multiple mechanisms are implicated in the generation of 5q35 microdeletions in Sotos syndrome. J Med Genet (2005) 1.06
Partial urorectal septum malformation sequence: a report of 25 cases. Am J Med Genet (2001) 1.04
Aarskog syndrome. New findings and genetic analysis. JAMA (1978) 1.04
Weaver syndrome: autosomal dominant inheritance of the disorder. Am J Med Genet (1998) 1.04
Failure of X inactivation in the autosomal segment of an X/A translocation. Am J Hum Genet (1980) 1.03
Radical radiotherapy for stage I/II non-small cell lung cancer in patients not sufficiently fit for or declining surgery (medically inoperable). Cochrane Database Syst Rev (2001) 1.03
Involvement of the gastrointestinal tract by metastases from germ cell tumors of the testis. Cancer (1988) 1.02
Distal 13q Deletion Syndrome and the VACTERL association: case report, literature review, and possible implications. Am J Med Genet (2001) 1.02
A mutation that causes lability of the androgen receptor under conditions that normally promote transformation to the DNA-binding state. J Clin Invest (1984) 1.02
"Bridging bronchus". A previously undescribed airway anomaly. Am J Dis Child (1976) 1.01
Mutations in JARID1C are associated with X-linked mental retardation, short stature and hyperreflexia. J Med Genet (2008) 1.01
Comparison of analysis of variance and maximum likelihood based path analysis of twin data: partitioning genetic and environmental sources of covariance. Genet Epidemiol (1995) 1.01
Autosomal dominant branchiootorenal dysplasia. Birth Defects Orig Artic Ser (1975) 1.01
Type IX Ehlers-Danlos syndrome. A new variant with pathognomonic radiographic features. Radiology (1984) 1.01
Development of CD4+CD8+ thymocytes in RAG-deficient mice through a T cell receptor beta chain-independent pathway. J Exp Med (1995) 1.00
Response of differentiated but not anaplastic teratoma to interferon. Br J Cancer (1984) 1.00
Multiclonal outbreak of methicillin-resistant Staphylococcus aureus infections on a collegiate football team. Epidemiol Infect (2008) 0.99
Management of trials in the development of cancer chemotherapy. Br J Cancer (1978) 0.99
Cartilage-hair hypoplasia, defective T-cell function, and Diamond-Blackfan anemia in an Amish child. Am J Med Genet (1981) 0.98
The discrimination of phenotypes for rate of disappearance of isonicotinoyl hydrazide from serum. J Clin Invest (1969) 0.98
Possible localization of a major gene for cleft lip and palate to 4q. Clin Genet (1994) 0.98
Acid resistance of Escherichia coli O157:H7 from the gastrointestinal tract of cattle fed hay or grain. Vet Microbiol (2003) 0.98
Radical radiotherapy for stage I/II non-small cell lung cancer in patients not sufficiently fit for or declining surgery (medically inoperable). Cochrane Database Syst Rev (2001) 0.97
Facial clefts in Danish twins. Cleft Palate J (1979) 0.97
Dicentric chromosome 13 and centromere inactivation. Hum Genet (1983) 0.97
Genitourinary anomalies in the CHARGE association. J Urol (1999) 0.97