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Genetic Counseling (Geneva, Switzerland)|January 31, 2006
Apert syndrome with preaxial polydactyly showing the typical mutation Ser252Trp in the FGFR2 geneJ M Mantilla-Capacho, L Arnaud, M Díaz-Rodriguez, et al.Genetic Counseling (Geneva, Switzerland)|February 12, 2002
The 4q-SyndromeE M Strehle, O A Ahmed, M Hameed, et al.Genetic Counseling (Geneva, Switzerland)|February 12, 2002
Intrafamilial clinical variability in type C brachydactylyP Debeer, L De Smet, J P FrynsGenetic Counseling (Geneva, Switzerland)|February 12, 2002
Interchange trisomy 21 by t(1;21)(p22;q22)matM G Dominguez, H Rivera, A I Vasquez, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1991
Pericentric inversion of chromosome 13: familial study and review of the literatureC Fernández-Novoa, T Vargas, J M Fernández-Ortega, et al.Genetic Counseling (Geneva, Switzerland)|October 20, 1998
Mutation analysis of the HLA-H gene in French hemochromatosis patients, and genetic counseling in familiesG Mercier, A Burckel, C Bathelier, et al.Genetic Counseling (Geneva, Switzerland)|January 23, 1999
Linkage analysis excludes familial congenital hypothyroidism from chromosome 21B E Ahlbom, M Yaqoob, G Annerén, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1992
Apert syndrome with partial preaxial polydactylyG Lefort, P Sarda, C Humeau, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1992
A syndrome of mental retardation, short stature, craniofacial anomalies with palpebral ptosis and pulmonary stenosis in three siblings with normal parents. An example of autosomal recessive inheritance of the Noonan phenotype?C Maximilian, D M Ioan, J P FrynsGenetic Counseling (Geneva, Switzerland)|January 1, 1992
Partial monosomy 8p and partial trisomy 8p with moderate mental retardationI D van Balkom, J Hagendoorn, J M De Pater, et al.Pageof 116