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Birth Defects Original Article Series|January 1, 1981
Cutaneous manifestation of neurofibromatosis: cellular interaction, pigmentation, and mast cellsV M RiccardiBirth Defects Original Article Series|January 1, 1980
Dental diagnostic problems of potential genetic significance: the dental practitioner as geneticist in the developmental disabilities clinicH Diner, M D ChouBirth Defects Original Article Series|January 1, 1982
Duncan Guthrie Institute of Medical Genetics, Glasgow, University of Glasgow, ScotlandM A Ferguson-Smith, D A AitkenBirth Defects Original Article Series|January 1, 1977
Syndrome of myopathy, short stature, seizures, retinitis pigmentosa, and cleft lipS L Yong, R B Lowry, J E JanBirth Defects Original Article Series|January 1, 1977
The WT syndrome--a "new" autosomal dominant pleiotropic trait of radial/ulnar hypoplasia with high risk of bone marrow failure and/or leukemiaC H Gonzalez, M V Durkin-Stamm, N F Geimer, et al.Birth Defects Original Article Series|January 1, 1977
The course of the cerebrocostomandibular syndromeD J Harris, R A FellowsBirth Defects Original Article Series|January 1, 1977
Are the acrocephalosyndactyly syndromes variable expressions of a single gene defect?V Escobar, D BixlerBirth Defects Original Article Series|January 1, 1977
Autosomal recessive hypohidrotic ectodermal dysplasia with subclinical manifestation in the heterozygoteE Passarge, E FriesBirth Defects Original Article Series|January 1, 1996
Multisite neural tube closure in humansM I Van AllenPageof 62