Published in Cleft Palate J on January 01, 1981
Epidemiological and genetic study in 207 cases of oral clefts in Alsace, north-eastern France. J Med Genet (1991) 1.00
Prevalence of congenital heart diseases in oral cleft patients. Pediatr Cardiol (2003) 0.90
A family study of isolated cleft palate. J Med Genet (1982) 0.84
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
Diagnostic criteria for the whistling face syndrome. Birth Defects Orig Artic Ser (1975) 1.09
Hypertelorism, microtia, and facial clefting. A newly described inherited syndrome. Am J Dis Child (1969) 1.07
Periodontosis: a phenotypic and genetic analysis. Oral Surg Oral Med Oral Pathol (1976) 1.07
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
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
Linkage studies in Van der Woude syndrome. J Med Genet (1978) 0.89
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
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
Analysis of intrafamilial correlations, serum levels of IGM and the human X-chromosome. Hum Hered (1979) 0.82
Anthropometric analysis of the face in hypohidrotic ectodermal dysplasia: a family study. Am J Phys Anthropol (1987) 0.82
Bilateral macrostomia in one of monozygotic twins. Oral Surg Oral Med Oral Pathol (1984) 0.82
Microcephalic dwarfism in sisters. Birth Defects Orig Artic Ser (1974) 0.82
Serum alkaline phosphatase: normal values by sex and age. Clin Chem (1977) 0.82
X-linked (recessive) hypomaturation amelogenesis imperfecta: a prosthodontic, genetic, and histopathologic report. J Prosthet Dent (1991) 0.82
The human X-chromosome and the levels of serum immunoglobulin M. Clin Genet (1979) 0.81
Oral manifestations of acute leukemia in children. J Am Dent Assoc (1977) 0.81
Dentinogenesis imperfecta: genetic variations in a six-generation family. J Dent Res (1970) 0.80
Fetal mortality associated with cleft lip and cleft palate. Johns Hopkins Med J (1982) 0.80
Gustatory lacrimation in association with the branchio-oto-renal syndrome. Clin Genet (1985) 0.80
Unusual association of Saethre-Chotzen syndrome and congenital adrenal hyperplasia. Clin Genet (1977) 0.80
The syndrome of multisynostotic osteodysgenesis with long-bone fractures. Am J Med Genet (1980) 0.79
Blood and urinary fluoride studies following the ingestion of single dosages of fluoride. J Oral Ther Pharmacol (1966) 0.79
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
Bone dysplasias: the prenatal diagnostic challenge. Am J Med Genet (1990) 0.78
Genetic counseling in dentistry. Dent Clin North Am (1975) 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
Agnathia-holoprosencephaly: a developmental field complex involving face and brain. Report of 3 cases. J Craniofac Genet Dev Biol Suppl (1985) 0.78
Radiographic hand abnormalities in fifteen cases of Crouzon syndrome. J Craniofac Genet Dev Biol (1982) 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
Fetal mortality in oral cleft families: data from Indiana and Montreal. Clin Genet (1983) 0.77
Antley-Bixler syndrome from a prognostic perspective: report of a case and review of the literature. Am J Med Genet (1988) 0.76
Genetic counseling in dentistry. J Dent Educ (1976) 0.76
Multifactorial threshold concept. Teratology (1978) 0.76
Quantitation of craniofacial anomalies in utero: fetal alcohol and Crouzon syndromes and thanatophoric dysplasia. Am J Med Genet (1993) 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
Dominantly inherited syndromic blepharophimosis. Am J Med Genet (1989) 0.75
Linkage analysis in dominant acrocephalosyndactyly. J Med Genet (1978) 0.75
Cleft lip and dermatoglyphic asymmetry. Am J Hum Genet (1977) 0.75
Effectiveness of a stannous fluoride-containing dentifrice in reducing dental caries in children in a boarding school environment. J Am Dent Assoc (1966) 0.75
[Juvenile polyposis of the colon]. Ann Radiol (Paris) (1976) 0.75
Familial reticulum cell sarcoma. Birth Defects Orig Artic Ser (1976) 0.75
Velopharyngeal variations in relatives of cleft-affected individuals. J Craniofac Genet Dev Biol (1985) 0.75
Fetal mortality in oral cleft families(IV): the "doubling effect". Clin Genet (1983) 0.75
Stickler syndrome: a cephalometric study of the face. J Craniofac Genet Dev Biol (1983) 0.75
Fetal mortality in oral cleft families (V): Studies of sporadic vs familial and pure vs syndromic clefts. Clin Genet (1984) 0.75
Facio-cardio-renal syndrome: a newly delineated recessive disorder. Clin Genet (1977) 0.75
Cleidocranial dysplasia-treatment of dental problems: report a case. ASDC J Dent Child (1982) 0.75
Uncritical use of the expression multifactorial threshold inheritance. Clin Genet (1976) 0.75
Lethal and mild hypophosphatasia in half-sibs. J Craniofac Genet Dev Biol (1982) 0.75
Clouston syndrome: an ultrastructural study. Clin Genet (1983) 0.75
Dominant inheritance of velopharyngeal incompetence. Clin Genet (1981) 0.75
Birth intervals in oral cleft families. Clin Genet (1985) 0.75
[Effect of use of a dentifrice with SnF2-ZrSi04]. Prev Stomatol (1978) 0.75
Popliteal pterygium syndrome in monozygous twins. Birth Defects Orig Artic Ser (1974) 0.75
Fetal mortality in oral cleft families (VI): a search for early embryonic and zygotic mortality. Clin Genet (1983) 0.75
The role of genetics in the practice of dentistry. J Indiana Dent Assoc (1981) 0.75
Fetal mortality in oral cleft families (VII): Birth intervals. Clin Genet (1984) 0.75
Autosomal dominant blepharophimosis with multiple congenital anomalies. J Clin Dysmorphol (1984) 0.75
Amelogenesis imperfecta and genetic counseling. J Oral Med (1974) 0.75
Developments in the trapezoidcephaly-multiple synostosis syndrome. Am J Med Genet (1983) 0.75
Fetal mortality in oral cleft families (X): a response. Clin Genet (1985) 0.75