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European Journal of Human Genetics : EJHG|March 14, 2000
Opposite deletions/duplications of the X chromosome: two novel reciprocal rearrangementsS Giglio, B Pirola, G Arrigo, et al.Genomics|February 15, 1997
Eleven X chromosome breakpoints associated with premature ovarian failure (POF) map to a 15-Mb YAC contig spanning Xq21C Sala, G Arrigo, G Torri, et al.American Journal of Human Genetics|April 29, 1998
A human homologue of the Drosophila melanogaster diaphanous gene is disrupted in a patient with premature ovarian failure: evidence for conserved function in oogenesis and implications for human sterilityS Bione, C Sala, C Manzini, et al.Genomics|February 28, 1998
Human NRD convertase: a highly conserved metalloendopeptidase expressed at specific sites during development and in adult tissuesP Fumagalli, M Accarino, A Egeo, et al.Human Molecular Genetics|April 18, 1998
The mouse Mid1 gene: implications for the pathogenesis of Opitz syndrome and the evolution of the mammalian pseudoautosomal regionL Dal Zotto, N A Quaderi, R Elliott, et al.Journal of Medical Genetics|September 4, 2007
Cryptic deletions are a common finding in "balanced" reciprocal and complex chromosome rearrangements: a study of 59 patientsM De Gregori, R Ciccone, P Magini, et al.Pageof 4