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Genetic Counseling (Geneva, Switzerland)|October 27, 2009
A Feingold syndrome case with previously undescribed features and a new mutationH Koçak, E Ozaydin, G Köse, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1997
Patterns of meiotic variability of the (CAG)n repeat in the Huntington disease geneG Lucotte, N Gérard, A Aouizérate, et al.Genetic 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)|January 1, 1997
Brachydactyly and short stature in a mother and her daughter with a fragile site at 16q22C Stoll, B Roy-Doray, B Dott, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1994
Genetic basis of developmental dysphasia. Report of eleven familial cases in six familiesC Billard, A Toutain, M L Loisel, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1994
Oto-palato-digital syndrome type IIC Stoll, Y AlembikGenetic Counseling (Geneva, Switzerland)|January 1, 1994
Thrombocytopenia and cleft hand in monosomy 21A Vogels, L de Smet, H van den Berghe, et al.Genetic Counseling (Geneva, Switzerland)|November 2, 2005
M-FISH applications in clinical geneticsZ Cetin, S Berker Karaüzüm, S Yakut, et al.Genetic Counseling (Geneva, Switzerland)|November 2, 2005
Report of a patient with a trisomy of chromosome region 20q11.2-->20q12 and characterization with FISHH Y C Wanderley, C T R M Schrander-Stumpel, M O J M Visser, et al.Genetic Counseling (Geneva, Switzerland)|November 2, 2005
Robinow Syndrome: a case reportH Gulcan, A Akinci, A AktarPageof 116