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Genetic Counseling (Geneva, Switzerland)|January 23, 1999
Terminal deletion of chromosome 10q26: delineation of two clinical phenotypesP Petit, K Devriendt, M Azou, et al.Genetic Counseling (Geneva, Switzerland)|January 23, 1999
Progressive pseudorheumatoid dysplasia: report of a patient with symptoms present at birthG van Buggenhout, L De Smet, P Maroteaux, et al.Genetic Counseling (Geneva, Switzerland)|January 23, 1999
Syndrome of myxomas, spotty skin pigmentation, and endocrine overactivity (Carney complex)E Legius, W Daenen, V Vandenbergh, et al.Genetic Counseling (Geneva, Switzerland)|October 20, 1998
Localization by FISH of centric fission breakpoints in a de novo trisomy 9p patient with i(9p) and t(9q;11p)P Petit, K Devriendt, J R Vermeesch, et al.Genetic Counseling (Geneva, Switzerland)|January 31, 2006
Chromosomal region 13q21q31 and heterochrony of developmentC Stoll, V Martel-PetitGenetic Counseling (Geneva, Switzerland)|January 31, 2006
Double aneuploidy in three Egyptian patients: Down-Turner and Down-Klinefelter syndromesM S Zaki, A A Kamel, M El-RubyGenetic Counseling (Geneva, Switzerland)|January 1, 1997
Complete androgen insensitivity syndrome: clinical and anatomopathological findings in 23 patientsF Alvarez-Nava, S Gonzalez, M Soto, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1997
Del(4)(pter-->q33:) case report and review of the literatureP Grammatico, L Spaccini, C Di Rosa, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1996
Nager acrofacial dysostosis. An adult male with severe neurological deficitJ P Fryns, A Bonhomme, H Van den BergheGenetic Counseling (Geneva, Switzerland)|April 7, 1999
Congenital heart defects in patients with DiGeorge/velocardiofacial syndrome and del22q11B Marino, M C Digilio, A Toscano, et al.Pageof 116