Linkage studies in Van der Woude syndrome.

Linkage of an autosomal dominant clefting syndrome (Van der Woude) to loci on chromosome Iq. Am J Hum Genet (1990) 1.48

Linkage studies in a pedigree with Van der Woude syndrome. J Med Genet (1987) 0.79

A general model for the genetic analysis of pedigree data. Hum Hered (1971) 40.17

Estimation of the recombination fraction in human pedigrees: efficient computation of the likelihood for human linkage studies. Am J Hum Genet (1974) 23.66

Fistula labii inferioris congenita and its association with cleft lip and palate. Am J Hum Genet (1954) 3.38

The syndrome of pits of the lower lip and cleft lip and/or palate. Genetic considerations. Am J Hum Genet (1967) 2.32

Lip pits and congenital absence of second premolars: varied expression of the Lip Pits syndrome. J Med Genet (1973) 1.02

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

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

Segregation analysis of cleft lip with or without cleft palate: a comparison of Danish and Japanese data. Am J Hum Genet (1986) 2.23

A proposed classification for heritable human dentine defects with a description of a new entity. Arch Oral Biol (1973) 2.16

Improved outcome in Pierre Robin sequence: effect of multidisciplinary evaluation and management. Pediatrics (1990) 1.92

Multiple pterygium syndrome. Am J Dis Child (1978) 1.71

The ectrodactyly-ectodermal dysplasia-clefting (EEC) syndrome. Report of 2 cases and review of the literature. Clin Genet (1972) 1.63

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

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

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

Phenotypic variation in the popliteal pterygium syndrome. Clin Genet (1973) 1.21

Cleft palate: a genetic and epidemiologic investigation. Clin Genet (1981) 1.20

The acrocephalosyndactyly syndromes: a metacarpophalangeal pattern profile analysis. Clin Genet (1977) 1.18

On the classification of the acrocephalosyndactyly syndromes. Clin Genet (1977) 1.15

Phenotypic and genetic analysis of the silver-Russell syndrome. Clin Genet (1978) 1.11

Diagnostic criteria for the whistling face syndrome. Birth Defects Orig Artic Ser (1975) 1.09

Periodontosis: a phenotypic and genetic analysis. Oral Surg Oral Med Oral Pathol (1976) 1.07

THE X-RAY IN WAR SURGERY AND ITS RELATION TO THE REMOVAL OF FOREIGN BODIES: SPECIAL REFERENCE TO OPERATING WITH SYNCHRONOUS ASSISTANCE OF THE FLUOROSCOPE. Ann Surg (1917) 1.07

Hypertelorism, microtia, and facial clefting. A newly described inherited syndrome. Am J Dis Child (1969) 1.07

Autosomal dominant maxillofacial dysostosis. Birth Defects Orig Artic Ser (1977) 1.06

Aarskog syndrome. New findings and genetic analysis. JAMA (1978) 1.04

The combined employee health risk--occupational hazard appraisal: the New York City experience. J Public Health Policy (1988) 1.03

Popliteal pterygium syndrome: a phenotypic and genetic analysis. J Med Genet (1978) 1.01

Autosomal dominant branchiootorenal dysplasia. Birth Defects Orig Artic Ser (1975) 1.01

Multiclonal outbreak of methicillin-resistant Staphylococcus aureus infections on a collegiate football team. Epidemiol Infect (2008) 0.99

Possible localization of a major gene for cleft lip and palate to 4q. Clin Genet (1994) 0.98

Facial clefts in Danish twins. Cleft Palate J (1979) 0.97

Facial clefting: an alternative biologic explanation for its complex etiology. Birth Defects Orig Artic Ser (1977) 0.96

Genetics and clefting. Cleft Palate J (1981) 0.95

Clinical, laboratory, and genetic investigations of hypophosphatasia: support for autosomal dominant inheritance with homozygous lethality. J Craniofac Genet Dev Biol (1983) 0.93

Familial aortic dissection with iris anomalies--a new connective tissue disease syndrome? Birth Defects Orig Artic Ser (1976) 0.92

Facial morphometrics in the identification of gene carriers of X-linked hypohidrotic ectodermal dysplasia. Am J Med Genet (1990) 0.91

Human parotid proline-rich proteins: correlation of genetic polymorphisms to dental caries. Genet Epidemiol (1986) 0.90

Probable autosomal recessive inheritance of polysplenia, situs inversus and cardiac defects in an Amish family. Am J Med Genet (1983) 0.89

Radiographic appearance of the cervical vertebrae in normal and abnormal development. Br J Oral Surg (1982) 0.88

Femoral hypoplasia-unusual facies syndrome, from another viewpoint. Eur J Pediatr (1978) 0.88

Studies of cleft lip and cleft palate in the population of Denmark. Prog Clin Biol Res (1980) 0.88

The effects of changing caries prevalence and diagnostic criteria on clinical caries trials. Caries Res (1983) 0.87

Fetal mortality in oral cleft families (IX): factors relating to the occurrence of sporadic clefts. Clin Genet (1984) 0.87

Gingival fibromatosis with sensorineural hearing loss: an autosomal dominant trait. Am J Med Genet (1985) 0.86

A study of cephalometric features in cleft lip-cleft palate families. I: Phenotypic heterogeneity and genetic predisposition in parents of sporadic cases. Cleft Palate J (1989) 0.85

Inherited factor X deficiency: presentation of a case with etiologic and treatment considerations. Oral Surg Oral Med Oral Pathol (1983) 0.85

Parent to child transmission of the thrombocytopenia absent radius (TAR) syndrome. Am J Med Genet Suppl (1986) 0.85

Cephalometric evidence for a dominantly inherited predisposition to cleft lip-cleft palate in a single large kindred. Am J Med Genet (1994) 0.85

Interradicular dentin dysplasia associated with amelogenesis imperfecta. Oral Surg Oral Med Oral Pathol (1985) 0.83

Clouston syndrome: a rare autosomal dominant trait with palmoplantar hyperkeratosis and alopecia. J Craniofac Genet Dev Biol (1992) 0.83

Periodontal disease in diabetics. J Periodontol (1967) 0.82

Anthropometric analysis of the face in hypohidrotic ectodermal dysplasia: a family study. Am J Phys Anthropol (1987) 0.82

X-linked (recessive) hypomaturation amelogenesis imperfecta: a prosthodontic, genetic, and histopathologic report. J Prosthet Dent (1991) 0.82

Serum alkaline phosphatase: normal values by sex and age. Clin Chem (1977) 0.82

Analysis of intrafamilial correlations, serum levels of IGM and the human X-chromosome. Hum Hered (1979) 0.82

Microcephalic dwarfism in sisters. Birth Defects Orig Artic Ser (1974) 0.82

Bilateral macrostomia in one of monozygotic twins. Oral Surg Oral Med Oral Pathol (1984) 0.82

Oral manifestations of acute leukemia in children. J Am Dent Assoc (1977) 0.81

Familial facial asymmetry (autosomal dominant hemihypertrophy?). Oral Surg Oral Med Oral Pathol (1980) 0.81

The human X-chromosome and the levels of serum immunoglobulin M. Clin Genet (1979) 0.81

Fetal mortality associated with cleft lip and cleft palate. Johns Hopkins Med J (1982) 0.80

Unusual association of Saethre-Chotzen syndrome and congenital adrenal hyperplasia. Clin Genet (1977) 0.80

Dentinogenesis imperfecta: genetic variations in a six-generation family. J Dent Res (1970) 0.80

Gustatory lacrimation in association with the branchio-oto-renal syndrome. Clin Genet (1985) 0.80

Blood and urinary fluoride studies following the ingestion of single dosages of fluoride. J Oral Ther Pharmacol (1966) 0.79

The syndrome of multisynostotic osteodysgenesis with long-bone fractures. Am J Med Genet (1980) 0.79

Focal odontoblastic dysplasia: dentin dysplasia type III? Oral Surg Oral Med Oral Pathol (1977) 0.79

Bone dysplasias: the prenatal diagnostic challenge. Am J Med Genet (1990) 0.78

Genetic counseling in dentistry. Dent Clin North Am (1975) 0.78

Agnathia-holoprosencephaly: a developmental field complex involving face and brain. Report of 3 cases. J Craniofac Genet Dev Biol Suppl (1985) 0.78

Generalized cortical hyperostosis (Van Buchem disease): nosologic considerations. Radiology (1977) 0.78

The effectiveness of iontophoresis in reducing cervical hypersensitivity. J Periodontol (1971) 0.78

Cleft lip, cleft palate, and congenital fistulas of the lower lip. Report of a familial occurrence. Oral Surg Oral Med Oral Pathol (1967) 0.78

Fetal mortality in oral cleft families: data from Indiana and Montreal. Clin Genet (1983) 0.77

The dentition of the Queckchi Indians. Anthropological aspects. Am J Phys Anthropol (1977) 0.77

Fetal mortality and cleft lip with or without cleft palate. Clin Genet (1983) 0.77

An incident of familial cancer, including 3 cases of osteogenic sarcoma. Cancer (1970) 0.77

Radiographic hand abnormalities in fifteen cases of Crouzon syndrome. J Craniofac Genet Dev Biol (1982) 0.77

Hemangioma-like lesions: diagnosis and management. Gen Dent (1998) 0.77

Ultrafiltrable calcium and the conformation of albumin. Clin Chim Acta (1975) 0.76

Quantitation of craniofacial anomalies in utero: fetal alcohol and Crouzon syndromes and thanatophoric dysplasia. Am J Med Genet (1993) 0.76

Genetic counseling in dentistry. J Dent Educ (1976) 0.76

Multifactorial threshold concept. Teratology (1978) 0.76

A clinical, genetic, and ultrastructural study of snow-capped teeth: amelogenesis imperfecta, hypomaturation type. Oral Surg Oral Med Oral Pathol (1981) 0.76

Antley-Bixler syndrome from a prognostic perspective: report of a case and review of the literature. Am J Med Genet (1988) 0.76

Cleft lip and dermatoglyphic asymmetry. Am J Hum Genet (1977) 0.75

Linkage analysis in dominant acrocephalosyndactyly. J Med Genet (1978) 0.75