Published in Arch Oral Biol on April 01, 1973
Hereditary dentine disorders: dentinogenesis imperfecta and dentine dysplasia. Orphanet J Rare Dis (2008) 1.66
A novel splice acceptor mutation in the DSPP gene causing dentinogenesis imperfecta type II. Hum Genet (2004) 1.45
Disorders of human dentin. Cells Tissues Organs (2007) 1.37
Mutational hot spot in the DSPP gene causing dentinogenesis imperfecta type II. Hum Genet (2004) 1.26
Signaling networks regulating tooth organogenesis and regeneration, and the specification of dental mesenchymal and epithelial cell lineages. Cold Spring Harb Perspect Biol (2012) 1.14
Astacin proteases cleave dentin sialophosphoprotein (Dspp) to generate dentin phosphoprotein (Dpp). J Bone Miner Res (2011) 1.08
Tooth dentin defects reflect genetic disorders affecting bone mineralization. Bone (2012) 1.07
A dentin sialophosphoprotein mutation that partially disrupts a splice acceptor site causes type II dentin dysplasia. J Endod (2008) 1.03
Rough endoplasmic reticulum trafficking errors by different classes of mutant dentin sialophosphoprotein (DSPP) cause dominant negative effects in both dentinogenesis imperfecta and dentin dysplasia by entrapping normal DSPP. J Bone Miner Res (2012) 1.03
A novel DSPP mutation is associated with type II dentinogenesis imperfecta in a Chinese family. BMC Med Genet (2007) 1.02
Dental abnormalities in Schimke immuno-osseous dysplasia. J Dent Res (2012) 0.95
Dentinogenesis imperfecta type I: A case report with literature review on nomenclature system. J Oral Maxillofac Pathol (2014) 0.95
Phenotypic variation in dentinogenesis imperfecta/dentin dysplasia linked to 4q21. J Dent Res (2006) 0.95
Isolated dentinogenesis imperfecta and dentin dysplasia: revision of the classification. Eur J Hum Genet (2014) 0.92
Roles of heparan sulfate sulfation in dentinogenesis. J Biol Chem (2012) 0.89
Dentinogenesis and Dentin Sialophosphoprotein (DSPP). J Oral Biosci (2009) 0.89
Porcine dentin sialoprotein glycosylation and glycosaminoglycan attachments. BMC Biochem (2011) 0.84
Immunocytochemical detection of dentin matrix proteins in primary teeth from patients with dentinogenesis imperfecta associated with osteogenesis imperfecta. Eur J Histochem (2014) 0.81
Dentin dysplasia type I: a challenge for treatment with dental implants. Head Face Med (2007) 0.81
Phenotype characterization and DSPP mutational analysis of three Brazilian dentinogenesis imperfecta type II families. Cells Tissues Organs (2008) 0.80
Dental Management of a Child with Dentinogenesis Imperfecta: A Case Report. J Dent (Tehran) (2016) 0.80
Essential Roles of Bone Morphogenetic Protein-1 and Mammalian Tolloid-like 1 in Postnatal Root Dentin Formation. J Endod (2016) 0.79
Dentin phosphoprotein gene locus is not associated with dentinogenesis imperfecta types II and III. Am J Hum Genet (1992) 0.79
Multiple pulp stones: a case report. Eur J Dent (2011) 0.78
A DSPP mutation causing dentinogenesis imperfecta and characterization of the mutational effect. Biomed Res Int (2012) 0.78
Clinical manifestations and dental management of dentinogenesis imperfecta associated with osteogenesis imperfecta: Case report. Saudi Dent J (2013) 0.77
N-terminal Dentin Sialoprotein fragment induces type I collagen production and upregulates dentinogenesis marker expression in osteoblasts. Biochem Biophys Rep (2016) 0.77
Root anomalies and dentin dysplasia in autosomal recessive hyperphosphatemic familial tumoral calcinosis (HFTC). Oral Surg Oral Med Oral Pathol Oral Radiol (2015) 0.77
Malformations of the tooth root in humans. Front Physiol (2015) 0.76
Klf10 regulates odontoblast differentiation and mineralization via promoting expression of dentin matrix protein 1 and dentin sialophosphoprotein genes. Cell Tissue Res (2015) 0.76
Site-specific function and regulation of Osterix in tooth root formation. Int Endod J (2016) 0.76
Dentin dysplasia type I. BMJ Case Rep (2013) 0.75
Prosthodontic rehabilitation of dentinogenesis imperfecta. Contemp Clin Dent (2011) 0.75
Dentin dysplasia type I-novel findings in deciduous and permanent teeth. BMC Oral Health (2015) 0.75
The dentin phosphoprotein repeat region and inherited defects of dentin. Mol Genet Genomic Med (2015) 0.75
Detection of a Novel DSPP Mutation by NGS in a Population Isolate in Madagascar. Front Physiol (2016) 0.75
Hereditary dentine dysplasias: terminology in the context of osteogenesis imperfecta. Br Dent J (2016) 0.75
Prevalence of Dentinogenesis Imperfecta in a French Population. J Int Soc Prev Community Dent (2017) 0.75
Hereditary opalescent dentin. BMJ Case Rep (2013) 0.75
Dentinal dysplasia type I: a case report with a 6-year followup. Case Rep Dent (2013) 0.75
Dentin dysplasia type I - A rare entity. J Oral Maxillofac Pathol (2015) 0.75
Amelogenesis imperfecta: review of diagnostic findings and treatment concepts. Odontology (2016) 0.75
Dentinogenesis imperfecta type II: A case report with 17 years of follow-up. Imaging Sci Dent (2017) 0.75
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
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
Allelic restriction: a biologic alternative to multifactorial threshold inheritance. Lancet (1976) 1.10
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
Genetic epidemiology of the susceptibility to leprosy. J Clin Invest (1987) 1.07
Hypertelorism, microtia, and facial clefting. A newly described inherited syndrome. Am J Dis Child (1969) 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
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
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
Tricho-dento-osseous syndrome: a scanning electron microscopic analysis. Clin Genet (1977) 0.87
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
Orofaciodigital syndrome, type I: a phenotypic and genetic analysis. Oral Surg Oral Med Oral Pathol (1975) 0.85
Aarskog syndrome: new oral-facial findings. Clin Genet (1976) 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
Clouston syndrome: a rare autosomal dominant trait with palmoplantar hyperkeratosis and alopecia. J Craniofac Genet Dev Biol (1992) 0.83
Interradicular dentin dysplasia associated with amelogenesis imperfecta. Oral Surg Oral Med Oral Pathol (1985) 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
Analysis of intrafamilial correlations, serum levels of IGM and the human X-chromosome. Hum Hered (1979) 0.82
Bilateral macrostomia in one of monozygotic twins. Oral Surg Oral Med Oral Pathol (1984) 0.82
Serum alkaline phosphatase: normal values by sex and age. Clin Chem (1977) 0.82
Microcephalic dwarfism in sisters. Birth Defects Orig Artic Ser (1974) 0.82
Cavitation defects on the lingual ramus: a further expression of Stafne's defect. J Craniofac Genet Dev Biol (1992) 0.81
Oral manifestations of acute leukemia in children. J Am Dent Assoc (1977) 0.81
The human X-chromosome and the levels of serum immunoglobulin M. Clin Genet (1979) 0.81
Unusual association of Saethre-Chotzen syndrome and congenital adrenal hyperplasia. Clin Genet (1977) 0.80
Fetal mortality associated with cleft lip and cleft palate. Johns Hopkins Med J (1982) 0.80
Dentinogenesis imperfecta: genetic variations in a six-generation family. J Dent Res (1970) 0.80
Locomotor phenotypes of unstimulated CD45RAhigh and CD45ROhigh CD4+ and CD8+ lymphocytes in three-dimensional collagen lattices. Immunology (1994) 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
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
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
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
A new classification of heritable human enamel defects and a discussion of dentin defects. Birth Defects Orig Artic Ser (1983) 0.78
Oral findings in patients with autosomal dominant hypophosphatemic bone disease and X-linked hypophosphatemia: further evidence that they are different diseases. Oral Surg Oral Med Oral Pathol (1988) 0.77
Fetal mortality in oral cleft families: data from Indiana and Montreal. Clin Genet (1983) 0.77
Radiographic hand abnormalities in fifteen cases of Crouzon syndrome. J Craniofac Genet Dev Biol (1982) 0.77
Locomotory characteristics of fibroblasts within a three-dimensional collagen lattice: modulation by a helium/neon soft laser. Lasers Surg Med (1992) 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
Genetic counseling in dentistry. J Dent Educ (1976) 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
Quantitation of craniofacial anomalies in utero: fetal alcohol and Crouzon syndromes and thanatophoric dysplasia. Am J Med Genet (1993) 0.76
Multifactorial threshold concept. Teratology (1978) 0.76
Linkage analysis in dominant acrocephalosyndactyly. J Med Genet (1978) 0.75
Cleft lip and dermatoglyphic asymmetry. Am J Hum Genet (1977) 0.75
Dominantly inherited syndromic blepharophimosis. Am J Med Genet (1989) 0.75
Facio-cardio-renal syndrome: a newly delineated recessive disorder. Clin Genet (1977) 0.75
The oral-facial geneticist: his training and role in dentistry. J Dent Educ (1977) 0.75
Fetal craniofacial morphometrics: in utero evaluation at 16 weeks' gestation. Obstet Gynecol (1988) 0.75
[Juvenile polyposis of the colon]. Ann Radiol (Paris) (1976) 0.75
Renal agenesis with meningomyelocele and absence of Müllerian structures. Am J Med Genet (1988) 0.75
Uncritical use of the expression multifactorial threshold inheritance. Clin Genet (1976) 0.75
[Effect of use of a dentifrice with SnF2-ZrSi04]. Prev Stomatol (1978) 0.75
Familial reticulum cell sarcoma. Birth Defects Orig Artic Ser (1976) 0.75