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Genetic Counseling (Geneva, Switzerland)|January 1, 1993
Oculo-auriculo-vertebral spectrum malformation and contralateral absence of internal carotid arteryE Legius, M Hellemans, G Wilms, et al.Clinical Genetics|March 1, 1987
Unusual in vivo rearrangements of the Y-chromosome in two malesJ P Fryns, A Kleczkowska, P Lemmens, et al.Clinical Genetics|January 1, 1988
Isolated mesomelic shortening of the forearm in father and daughter: a new entity in the group of mesomelic dysplasiasJ P Fryns, G Hofkens, G Fabry, et al.Annales De Genetique|January 1, 1989
Normal phenotype and slight mental retardation in de novo distal 8p deletion (8pter----8p23.1:)J P Fryns, A Kleczkowska, A Vogels, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1991
Noonan phenotype in the basal cell nevus syndromeC Grubben, J P Fryns, E Smeets, et al.Journal of Medical Genetics|November 1, 1990
MASA syndrome: new clinical features and linkage analysis using DNA probesC Schrander-Stumpel, E Legius, J P Fryns, et al.Virchows Archiv : an International Journal of Pathology|March 21, 1998
Adenoid cystic carcinoma arising in an adenomyoepithelioma of the breastJ Van Dorpe, A De Pauw, P MoermanInternational Journal of Gynecological Cancer : Official Journal of the International Gynecological Cancer Society|June 29, 2006
Second case of uterine mesonephric adenocarcinomaA Marquette, P Moerman, I Vergote, et al.American Journal of Medical Genetics|March 1, 1987
Mental retardation, deafness, skeletal abnormalities, and coarse face with full lips: confirmation of the Fountain syndromeJ P Fryns, A Dereymaeker, M Hoefnagels, et al.Clinical Genetics|February 1, 1986
Population cytogenetics of autosomal fragile sitesP Petit, J P Fryns, H van den Berghe, et al.Pageof 89