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Genetic Counseling (Geneva, Switzerland)|January 1, 1993
Miller postaxial acrofacial dysostosis. The phenotypic changes with ageK Chrzanowska, J P FrynsJournal De Genetique Humaine|September 1, 1989
[Tetrasomy 12p (Pallister-Killian syndrome): possible diagnosis before the age of a year]K Chrzanowska, J P FrynsJournal of Medical Genetics|August 1, 1989
Hypohidrotic ectodermal dysplasia, primary hypothyroidism, and agenesis of the corpus callosumJ P Fryns, K Chrzanowska, H Van den BergheAmerican Journal of Medical Genetics|August 1, 1989
Cardio-facio-cutaneous (CFC) syndrome: report of a new patientK Chrzanowska, J P Fryns, H Van den BergheGenetic Counseling (Geneva, Switzerland)|January 5, 2001
MCA/MR syndrome with severe pre- and postnatal growth retardation, deep mental retardation, distinct facial appearance with nasal hypoplasia, cleft palate and retino-choroidal coloboma in two unrelated female patientsJ P FrynsAmerican Journal of Medical Genetics|April 1, 1992
Aarskog syndrome: the changing phenotype with ageJ P FrynsJournal De Genetique Humaine|January 1, 1988
[Balanced chromosome abnormalities with abnormal phenotype]J P FrynsAmerican Journal of Medical Genetics|January 1, 1986
The female and the fragile X. A study of 144 obligate female carriersJ P FrynsGenetic Counseling (Geneva, Switzerland)|January 1, 1994
Corpus callosum agenesis in Coffin-Lowry syndromeD Soekarman, J P FrynsPageof 81