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Clinical Genetics|October 1, 1994
Mild phenotype and normal gonadal function in females with 4p trisomy due to unbalanced t(X;4)(p22.1;p14)P Petit, C Hilliker, F Van Leuven, et al.Clinical Genetics|September 4, 1998
Marden-Walker syndrome versus isolated distal arthrogryposis: evidence that both conditions may be variable manifestations of the same mutated geneJ P Fryns, D Willekens, D Van Schoubroeck, et al.American Journal of Medical Genetics|February 15, 1992
Constrictive amniotic bands, amniotic adhesions, and limb-body wall complex: discrete disruption sequences with pathogenetic overlapP Moerman, J P Fryns, K Vandenberghe, et al.Prenatal Diagnosis|January 13, 1999
Prenatal diagnosis of de novo distal 5q duplication associated with hygroma colli, fetal oedema and complex cardiopathyI Witters, G Van Buggenhout, P Moerman, et al.American Journal of Medical Genetics|July 1, 1988
Caudal deficiency sequence in 7q terminal deletionC Schrander-Stumpel, J Schrander, J P Fryns, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1995
X-linked mental retardation and neurological symptoms: a nosological approachC T Schrander-Stumpel, C J Höweler, J P FrynsGenetic Counseling (Geneva, Switzerland)|January 1, 1997
The oculo-dento-digital syndrome: male-to-male transmission and variable expression in a familyD M Ioan, L Dumitriu, V Belengeariu, et al.Genetic Counseling (Geneva, Switzerland)|November 5, 1999
The concurrence of ring constrictions in Adams-Oliver syndrome: additional evidence for vascular disruption as common pathogenetic mechanismK Keymolen, L De Smet, P Bracke, et al.Clinical Genetics|September 1, 1993
Progressive pseudorheumatoid arthritis of childhood (PPAC) and normal adult heightE Legius, M Mulier, B Van Damme, et al.Genetic Counseling (Geneva, Switzerland)|February 1, 2003
Small terminal 10q26 deletion in a male patient with Noonan-like stigmata: diagnosis by cytogenetic and FISH analysisT Lukusa, E Smeets, J R Vermeesch, et al.Pageof 90