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Journal of Medical Genetics|January 15, 2003
The human Y chromosome's azoospermia factor b (AZFb) region: sequence, structure, and deletion analysis in infertile menA Ferlin, E Moro, A Rossi, et al.Acta Haematologica|January 1, 1979
Y chromosome duplication: a minor route evolutive pattern in CMLG Alimena, F Mandelli, A Montuoro, et al.Clinical Genetics|December 1, 1977
Translocation Y/5 resulting in Cri du Chat syndromeP Vignetti, L Chessa, L Bruni, et al.Human Genetics|August 1, 1989
Partial correction of chromosome instability in Fanconi anemia by desferrioxamineB Porfirio, G Ambroso, G Giannella, et al.Human Genetics|October 1, 1991
3' creatine kinase (M-type) polymorphisms linked to myotonic dystrophy in Italian and Spanish populationsM Gennarelli, G Novelli, A Cobo, et al.Annales De Genetique|January 1, 1991
Ring chromosome 14 syndrome. Report of two cases, including extended evaluation of a previously reported patient and reviewL Zelante, F Torricelli, S Calvano, et al.Bollettino Della Societa Italiana Di Biologia Sperimentale|January 1, 1989
[Construction of an apparatus for pulsed field electrophoresis for the analysis of high molecular weight DNA]M Gennarelli, G Novelli, A Ruzzo, et al.Pediatric Radiology|January 1, 1995
Spontaneous regression of exostoses: two case reportsA Castriota-Scanderbeg, M G Bonetti, M Cammisa, et al.American Journal of Medical Genetics|May 9, 2001
Congenital heart defects in Kabuki syndromeM C Digilio, B Marino, A Toscano, et al.Journal of Medical Genetics|October 1, 1980
De novo duplication 1q32-q42: variability of phenotypic features in partial lq trisomicsM S Lungarotti, A Falorni, A Calabro, et al.Pageof 34