Published in Clin Genet on May 01, 1985
Congenital aberrant tearing: a re-look. Trans Am Ophthalmol Soc (2008) 0.91
Genomewide search and genetic localization of a second gene associated with autosomal dominant branchio-oto-renal syndrome: clinical and genetic implications. Am J Hum Genet (2000) 0.86
Anatomical Changes and Audiological Profile in Branchio-oto-renal Syndrome: A Literature Review. Int Arch Otorhinolaryngol (2013) 0.82
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
Capsular management and refractive error in pediatric intraocular lenses. Ophthalmology (1997) 1.63
Surgical treatment of superior oblique palsy. Trans Am Ophthalmol Soc (1996) 1.60
Ocular lesions caused by caterpillar hairs (ophthalmia nodosa). Can J Ophthalmol (1984) 1.56
Early surgery for essential infantile esotropia. J Pediatr Ophthalmol Strabismus (1990) 1.48
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
Incidence of strabismus in neonates. Am J Ophthalmol (1985) 1.18
Surgical treatment of congenital esotropia. Am J Ophthalmol (1983) 1.17
The trochlea. A study of the anatomy and physiology. Ophthalmology (1982) 1.16
On the classification of the acrocephalosyndactyly syndromes. Clin Genet (1977) 1.15
Congenital blepharoptosis, anisometropia, and amblyopia. Am J Ophthalmol (1980) 1.14
Augmented recession of the medial recti. Ophthalmology (1978) 1.13
Surgical results of secondary glaucomas in childhood. Ophthalmology (1998) 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
Hypertelorism, microtia, and facial clefting. A newly described inherited syndrome. Am J Dis Child (1969) 1.07
Stereopsis in normal infants and infants with congenital esotropia. Am J Ophthalmol (1986) 1.06
Incidence of retinopathy of prematurity in a tertiary newborn intensive care unit. Arch Ophthalmol (1983) 1.05
X-linked recessive familial exudative vitreoretinopathy. Am J Ophthalmol (1992) 1.03
A new classification of superior oblique palsy based on congenital variations in the tendon. Ophthalmology (1992) 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
Persistent binocular diplopia after cataract surgery. Am J Ophthalmol (1987) 0.99
Visual function and academic performance. Am J Ophthalmol (1985) 0.98
Possible localization of a major gene for cleft lip and palate to 4q. Clin Genet (1994) 0.98
Microcephaly, microphthalmia, falciform retinal folds, and blindness. A new syndrome. Am J Dis Child (1981) 0.97
Facial clefts in Danish twins. Cleft Palate J (1979) 0.97
The geographic localization of presumed histoplasmic choroiditis. Am J Ophthalmol (1973) 0.96
Linear subcutaneous fat atrophy after corticosteroid injection of periocular hemangiomas. Am J Ophthalmol (1988) 0.96
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
Superior oblique palsy: diagnosis and classification. Int Ophthalmol Clin (1976) 0.94
Posterior scleral choristoma in the organoid nevus syndrome (linear nevus sebaceus of Jadassohn). Ophthalmology (1999) 0.94
Clinical, laboratory, and genetic investigations of hypophosphatasia: support for autosomal dominant inheritance with homozygous lethality. J Craniofac Genet Dev Biol (1983) 0.93
Superior oblique tuck for superior oblique palsy. Aust J Ophthalmol (1983) 0.92
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
Evaluation of an absorbable muscle sleeve to limit postoperative adhesions in strabismus surgery. Ophthalmic Surg (1987) 0.90
Optic chiasmatic glioma in children. Am J Ophthalmol (1979) 0.90
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
Large recession of the horizontal recti for treatment of nystagmus. Ophthalmology (1991) 0.89
Studies of cleft lip and cleft palate in the population of Denmark. Prog Clin Biol Res (1980) 0.88
Duane's retraction syndrome -- plus. J Pediatr Ophthalmol Strabismus (1982) 0.88
The effects of changing caries prevalence and diagnostic criteria on clinical caries trials. Caries Res (1983) 0.87
Congenital absence of the superior oblique tendon. Trans Am Ophthalmol Soc (1981) 0.87
Fetal mortality in oral cleft families (IX): factors relating to the occurrence of sporadic clefts. Clin Genet (1984) 0.87
Treatment of congenital glaucoma. Am J Ophthalmol (1981) 0.86
Adjustable sutures for horizontal and vertical strabismus. Am Orthopt J (1978) 0.86
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
The effect of tetracycline on the incidence of postextraction alveolar osteitis. J Oral Maxillofac Surg (1987) 0.84
Unilateral cataracts in children. Ophthalmic Surg (1980) 0.84
Silicone intubation in children with nasolacrimal obstruction. J Pediatr Ophthalmol Strabismus (1981) 0.84
Interradicular dentin dysplasia associated with amelogenesis imperfecta. Oral Surg Oral Med Oral Pathol (1985) 0.83
Aphakic cystoid macular edema in children. Arch Ophthalmol (1981) 0.83
Clouston syndrome: a rare autosomal dominant trait with palmoplantar hyperkeratosis and alopecia. J Craniofac Genet Dev Biol (1992) 0.83
Unilateral esotropia after enucleation in infancy. Am J Ophthalmol (1985) 0.83
Surgical management of strabismus associated with chronic progressive external ophthalmoplegia. Ophthalmology (1997) 0.83
Treatment of peripheral corneal ulcers by limlial conjunctivectomy. Br J Ophthalmol (1976) 0.83
Periodontal disease in diabetics. J Periodontol (1967) 0.82
Bilateral macrostomia in one of monozygotic twins. Oral Surg Oral Med Oral Pathol (1984) 0.82
Analysis of intrafamilial correlations, serum levels of IGM and the human X-chromosome. Hum Hered (1979) 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
Anthropometric analysis of the face in hypohidrotic ectodermal dysplasia: a family study. Am J Phys Anthropol (1987) 0.82
Microcephalic dwarfism in sisters. Birth Defects Orig Artic Ser (1974) 0.82
Filtering surgery in childhood glaucoma. Ophthalmic Surg (1984) 0.82
Strabismus surgery for endocrine ophthalmopathy. Ophthalmology (1979) 0.81
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
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
Cystoid macular edema in pediatric aphakia. J Pediatr Ophthalmol Strabismus (1988) 0.80
Dentinogenesis imperfecta: genetic variations in a six-generation family. J Dent Res (1970) 0.80
Comparison of temperaments of children with and without baby bottle tooth decay. ASDC J Dent Child (1998) 0.80
Surgical treatment of subluxated lenses in children. Ophthalmology (1992) 0.79
The syndrome of multisynostotic osteodysgenesis with long-bone fractures. Am J Med Genet (1980) 0.79
Vergence amplitudes with random-dot stereograms. Br J Ophthalmol (1986) 0.79