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Journal of Medical Genetics|February 1, 1979
Familial dicentric translocation t(13;18)(p13;p11.2) ascertained by recurrent miscarriagesA Daniel, I D Perel, A J Clarke, et al.Journal of Medical Genetics|June 1, 1979
Inherited anaemias in the Greek community of Cape TownR P Bonafede, M C Botha, P BeightonJournal of Medical Genetics|June 1, 1979
Triple mosaicism 45,XY,--18/46, XY/47,XY,+18M Frydman, F Shabtai, Y Barak, et al.Journal of Medical Genetics|June 1, 1979
The Prader-Willi syndrome with a 15/3 translocationM Kucerová, M Straková, Z PolívkováJournal of Medical Genetics|March 1, 1975
Prenatal diagnosis of a neural tube defect: Meckel syndromeM J SellerJournal of Medical Genetics|March 1, 1975
A case of hyalinosis cutis et mucosae (lipoid proteinosis of Urbach and Wiethe) with common ancestors in four remote generationsR C Juberg, P R Winder, L L TurkJournal of Medical Genetics|May 4, 2004
Functional dimorphism of two hAgRP promoter SNPs in linkage disequilibriumF Bai, T Rankinen, C Charbonneau, et al.Journal of Medical Genetics|June 21, 2005
Revisiting the craniosynostosis-radial ray hypoplasia association: Baller-Gerold syndrome caused by mutations in the RECQL4 geneL Van Maldergem, H A Siitonen, N Jalkh, et al.Journal of Medical Genetics|October 4, 2005
Matrilin-3 mutations that cause chondrodysplasias interfere with protein trafficking while a mutation associated with hand osteoarthritis does notC Otten, R Wagener, M Paulsson, et al.Journal of Medical Genetics|June 1, 1992
Experience with direct molecular diagnosis of fragile XJ C Mulley, S Yu, A K Gedeon, et al.Pageof 649