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Genetic Counseling (Geneva, Switzerland)|December 18, 2013
The clinical features and genetic mutations of chronic granulomatous disease: results from a reference centre at middle AnatoliaT Patiroglu, H Eke Gungor, E Unal, et al.
Genetic Counseling (Geneva, Switzerland)|April 28, 2010
Femoral bifurcation associated with tibial aplasia: about 3 casesM A Fiogbe, G M Hounnou, A S Gbenou, et al.
Genetic Counseling (Geneva, Switzerland)|April 28, 2010
Two cases of Sotos syndrome with novel mutations of the NSD1 geneH Fryssira, P Drossatou, R Sklavou, et al.
Genetic Counseling (Geneva, Switzerland)|April 28, 2010
A case with a rare chromosomal abnormality: isochromosome 18pM Dundar, A O Caglayan, C Saatci, et al.
Genetic Counseling (Geneva, Switzerland)|April 28, 2010
Benign familial macrocephaly in a mother-son pairM Díaz-Rodríguez, L E Becerra-Solano, J J Toscano-Flores, et al.
Genetic Counseling (Geneva, Switzerland)|April 28, 2010
Familial pericentric inversion of chromosome 18: intrafamilial variability of the recombinant dup(18q)P Prontera, B Buldrini, V Aiello, et al.
Genetic Counseling (Geneva, Switzerland)|April 28, 2010
A small (sSMC) chromosome 22 due to a maternal translocation between chromosomes 8 and 22: a case reportF E P Mundhofir, A J A Kooper, T I Winarni, et al.
Genetic Counseling (Geneva, Switzerland)|September 15, 2006
Constitutional duplication 11q23 de novo involving the MLL geneM Partida-Pérez, M G Domínguez, J Sánchez-Corona, et al.
Genetic Counseling (Geneva, Switzerland)|September 15, 2006
Direct transmission of the 18q- syndrome from mother to daughterC P Chen, S P Lin, S R Chern, et al.
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