Published in Dtsch Zahnarztl Z on February 01, 1977
Otodental syndrome. Orphanet J Rare Dis (2006) 0.92
Oral exophytic lesions in 23,616 white Americans over 35 years of age. Oral Surg Oral Med Oral Pathol (1986) 1.94
Hereditary defects of dentin. Dent Clin North Am (1975) 1.77
Visual system anomalies in human ocular albinos. Science (1978) 1.75
The Saethre-Chotzen syndrome. Birth Defects Orig Artic Ser (1975) 1.72
Asymmetric visually evoked potentials in human albinos: evidence for visual system anomalies. Invest Ophthalmol (1974) 1.66
Albinism. Surv Ophthalmol (1986) 1.41
Manifestations of genetic diseases in the human pulp. Oral Surg Oral Med Oral Pathol (1971) 1.40
Malformation syndromes. A selected miscellany. Birth Defects Orig Artic Ser (1975) 1.35
Autosomal recessively inherited ocular albinism. A new form of ocular albinism affecting females as severely as males. Arch Ophthalmol (1978) 1.33
Hermansky-Pudlak syndrome. Ophthalmic findings. Ophthalmology (1988) 1.26
Taurodontism, an isolated trait associated with syndromes and X-chromosomal aneuploidy. Am J Hum Genet (1980) 1.25
Medical and dental findings in the Brandywine isolate. Ala J Med Sci (1966) 1.24
Albinism. Adv Hum Genet (1971) 1.23
Autosomal recessive oculocutaneous albinism in man. Evidence for genetic heterogeneity. Am J Hum Genet (1970) 1.23
Basal cell nevus syndrome. Combined clinical staff conference at the National Institutes of Health. Ann Intern Med (1966) 1.20
Ophthalmologic, biochemical, platelet, and ultrastructural defects in the various types of oculocutaneous albinism. J Invest Dermatol (1973) 1.19
The Eurocleft project 1996-2000: overview. J Craniomaxillofac Surg (2001) 1.17
Abnormal visual pathways in the brain of a human albino. Brain Res (1975) 1.14
Studies of platelets in a variant of the Hermansky-Pudlak syndrome. Am J Pathol (1971) 1.13
Elevated urinary dolichol excretion in the Hermansky-Pudlak syndrome. Indicator of lysosomal dysfunction. Am J Med (1987) 1.12
Agenesis of succedaneous teeth: an expression of the homozygous state of the gene for the pegged or missing maxillary lateral incisor trait. Am J Med Genet (1987) 1.09
Partial expression of sex-linked recessive amelogenesis imperfecta in females compatible with the Lyon hypothesis. Oral Surg Oral Med Oral Pathol (1967) 1.08
The double-headed mandibular condyle. Oral Surg Oral Med Oral Pathol (1987) 1.08
Hypoplastic enamel, onycholysis, and hypohidrosis inherited as an autosomal dominant trait. A review of ectodermal dysplasia syndromes. Oral Surg Oral Med Oral Pathol (1975) 1.08
Inherited defects in tooth structure. Birth Defects Orig Artic Ser (1971) 1.07
Syndrome of amelogenesis imperfecta, nephrocalcinosis, impaired renal concentration, and possible abnormality of calcium metabolism. Am J Med Genet (1985) 1.05
Labile aggregation stimulating substance (LASS): the factor from storage pool deficient platelets correcting defective aggregation and release of aspirin treated normal platelets. Br J Haematol (1975) 1.05
Pathogenesis of pulmonary fibrosis: platelet-derived growth factor precedes structural alterations in the Hermansky-Pudlak syndrome. J Lab Clin Med (1994) 1.04
A single base insertion in the putative transmembrane domain of the tyrosinase gene as a cause for tyrosinase-negative oculocutaneous albinism. Proc Natl Acad Sci U S A (1991) 1.01
A frequent tyrosinase gene mutation associated with type I-A (tyrosinase-negative) oculocutaneous albinism in Puerto Rico. Am J Hum Genet (1993) 1.01
Hairbulb tyrosinase activity in oculocutaneous albinism. Nature (1976) 1.01
Heterogeneity in gingival fibromatosis. Birth Defects Orig Artic Ser (1971) 1.01
Detection of heterozygotes for tyrosinase-negative oculocutaneous albinism by hairbulb tyrosinase assay. Am J Hum Genet (1977) 1.00
Effects of normal and aspirin platelets on defective secondary aggregation in the Hermansky-Pudlak syndrome. A test for storage pool deficient platelets. Am J Pathol (1972) 1.00
Albinism in England. Birth Defects Orig Artic Ser (1982) 1.00
Hermansky-Pudlak syndrome in a Swiss population. Dermatology (1993) 0.99
Amish albinism: a distinctive autosomal recessive phenotype. Am J Hum Genet (1970) 0.98
Auditory brainstem anomalies in human albinos. Science (1980) 0.98
Hydro-jet cutting: a method for selective surgical dissection of nerve tissue. An experimental study on the sciatic nerve of rats. J Craniomaxillofac Surg (1999) 0.97
Autosomal recessive pigmented hypomaturation amelogenesis imperfecta. Report of a kindred. Oral Surg Oral Med Oral Pathol (1973) 0.97
Prevalence o f malocclusion in Chippewa Indian children. J Dent Res (1968) 0.96
Psychosocial factors in low-incidence genetic disease: the case of osteogenesis imperfecta. Soc Work Health Care (1976) 0.95
Combined chemical and electron microscopic studies of pheomelanosomes in human red hair. J Invest Dermatol (1983) 0.93
Autosomal dominant hypodontia with nail dysgenesis. Report of twenty-nine cases in six families. Oral Surg Oral Med Oral Pathol (1975) 0.92
Tyrosinase subcellular distribution and kinetic parameters in wild type and C-locus mutant C57BL/6J mice. J Exp Zool (1981) 0.92
Inherited disorders of pigmentation. Clin Dermatol (1986) 0.92
Clinical, histologic, cytologic, and ultrastructural characteristics of the oral lesions from hereditary mucoepithelial dysplasia. A disease of gap junction and desmosome formation. Oral Surg Oral Med Oral Pathol (1978) 0.92
Hereditary mucoepithelial dysplasia: a disease apparently of desmosome and gap junction formation. Am J Hum Genet (1979) 0.91
Albinism in Nigeria with delineation of new recessive oculocutaneous type. Clin Genet (1980) 0.91
Classification of albinism in man. Birth Defects Orig Artic Ser (1971) 0.91
Treatment of congenital anophthalmos with self-inflating polymer expanders: a new method. J Craniomaxillofac Surg (1999) 0.90
Clinical aspects of dental anomalies. Int Dent J (1976) 0.89
An improved method for the extraction of endogenous platelet serotonin. J Lab Clin Med (1976) 0.89
Incidence of velopharyngoplasty following various techniques of palatoplasty. J Craniomaxillofac Surg (1994) 0.89
Formhydroxamic acid-induced malformations of the temporo-mandibular joint. J Maxillofac Surg (1983) 0.87
Thioredoxin reductase activity in Hermansky-Pudlak syndrome: a method for identification of putative heterozygotes. J Invest Dermatol (1988) 0.87
The questionable relation between cochlear pigmentation and noise-induced hearing loss. Audiology (1985) 0.87
An electron optic analysis and explanation for the etiology of dentinal dysplasia. Oral Surg Oral Med Oral Pathol (1972) 0.87
Pulpal dysplasia. Oral Surg Oral Med Oral Pathol (1970) 0.86
Electromyography of oral-facial musculature in craniocarpaltarsal dysplasia (Freeman-Sheldon syndrome). Clin Genet (1974) 0.86
Auditory system abnormalities in human albinos. Ear Hear (1982) 0.86
Characterization of human hairbulb tyrosinase: properties of normal and albino enzyme. J Invest Dermatol (1978) 0.86
Odd tongues: the prevalence of common tongue lesions in 23,616 white Americans over 35 years of age. Quintessence Int (1986) 0.86
Odontogenic myxoma - clinical concept and morphological studies. J Oral Pathol (1977) 0.85
The influence of prostaglandin G2 on platelet ultrastructure and platelet secretion. Am J Pathol (1977) 0.85
Odd lips: the prevalence of common lip lesions in 23,616 white Americans over 35 years of age. Quintessence Int (1987) 0.84
Genetics and nutrition. Fed Proc (1967) 0.84
Perioperative antibiotic prophylaxis in maxillofacial surgery: penetration of clindamycin into various tissues. J Craniomaxillofac Surg (1999) 0.83
Albinism: hematologic-storage disease, susceptibility to skin cancer, and optic neuronal defects shared in all types of oculocutaneous and ocular albinism. Ala J Med Sci (1979) 0.83
Classification of facial malformations. Int J Oral Surg (1981) 0.83
Globodontia in the otodental syndrome. Oral Surg Oral Med Oral Pathol (1976) 0.83
Ultrastructural study of hereditary benign intraepithelial dyskeratosis. Oral Surg Oral Med Oral Pathol (1977) 0.82
Platelet aggregation independent of ADP release or prostaglandin synthesis in patients with hermansky-Pudlak syndrome. Prostaglandins Med (1981) 0.81
Quantification of a novel dense granule protein (granulophysin) in platelets of patients with dense granule storage pool deficiency. Blood (1992) 0.81
The presence of Candida albicans in hereditary benign intraepithelial dyskeratosis. An ultrastructural observation. Oral Surg Oral Med Oral Pathol (1979) 0.81
The Hermansky-Pudlak syndrome. Evidence for a lowered 5-hydroxytryptamine content in platelets of heterozygotes. Scand J Haematol (1977) 0.81
Closure of vertical alveolar bone defects with guided horizontal distraction osteogenesis: an experimental study in pigs and first clinical results. J Craniomaxillofac Surg (2001) 0.81
Electron optic microanalysis of two gene products in enamel of females heterozygous for X-linked hypomaturation amelogenesis imperfecta. Am J Hum Genet (1972) 0.81
Heterogeneity in inherited dental traits, gingival fibromatosis and amelogenesis imperfecta. South Med J (1971) 0.81
Pseudohypoparathyroidism. Oral Surg Oral Med Oral Pathol (1965) 0.81
Gardner's syndrome and other osteognathodermal disorders with defects in parathyroid functions. J Oral Surg (1968) 0.80
Is it possible to prevent cleft palate by prenatal administration of folic acid? An experimental study. Cleft Palate Craniofac J (2001) 0.80
Clinical, genetic, and histologic features of the trichoonychodental (TOD) syndrome. Oral Surg Oral Med Oral Pathol (1978) 0.79
[Mandibular condyle fractures in childhood--the clinico-roentgenological follow-up]. Dtsch Zahn Mund Kieferheilkd Zentralbl (1992) 0.79
Odontodysplasia. Report of three cases with vascular nevi overlying the adjacent skin of the face. Oral Surg Oral Med Oral Pathol (1978) 0.79
Dental implants in alveolar cleft patients: a retrospective study. J Craniomaxillofac Surg (1999) 0.78
[Contribution to the etiology and pathogenesis of chronic recurring parotitis]. Dtsch Zahnarztl Z (1979) 0.78
Tyrosinase positive oculocutaneous albinism among the Zuni and the Brandywine triracial isolate: biochemical and clinical characteristics and fertility. Am J Phys Anthropol (1972) 0.78
Molecular analyses of a tyrosinase-negative albino family. Am J Hum Genet (1993) 0.78
Late results following different methods of cleft lip repair. Cleft Palate J (1982) 0.78
Multiple basal cell carcinomas and keratocysts - the Gorlin and Goltz syndrome. J Maxillofac Surg (1979) 0.78
Hermansky-Pudlak syndrome (HPS): a proposed block in glutathione peroxidase. Oral Surg Oral Med Oral Pathol (1973) 0.78
Analysis of primary gingivoperiosteoplasty in alveolar cleft repair. Part I: Facial growth. J Craniomaxillofac Surg (1997) 0.77
p53 gene mutations and HPV infection in primary head and neck squamous cell carcinomas do not correlate with overall survival: a long-term follow-up study. J Oral Pathol Med (1997) 0.77
[Cleidocranial dysplasia--histological findings in the dental cementum]. Dtsch Zahnarztl Z (1978) 0.77
Chromosome breaks and sister chromatid exchanges in albinos in Nigeria. Clin Genet (1979) 0.76
The arrangement of muscle fibres in cleft lips. J Maxillofac Surg (1979) 0.76
Proceedings: Differences in platelet storage pool deficiency (SPD) of Hermansky Pudlak syndrome (HPS) and non-albinos (NA). Thromb Diath Haemorrh (1975) 0.76
Teeth with short, thin, dilacerated roots in patients with short stature: a dominantly inherited trait. Oral Surg Oral Med Oral Pathol (1982) 0.76