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American Journal of Human Genetics|May 1, 1995
Myotubular myopathy in a girl with a deletion at Xq27-q28 and unbalanced X inactivation assigns the MTM1 gene to a 600-kb regionN Dahl, L J Hu, M Chery, et al.Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|April 1, 1977
[X chromosome with deletion of the long arm]S Gilgenkrantz, G BauéAnnales De Genetique|January 1, 1988
Type C brachydactyly transmitted through four generationsJ Sanz, S GilgenkrantzGenomics|September 1, 1992
Chromosomal mapping of the human (MACS) and mouse (Macs) genes encoding the MARCKS proteinP J Blackshear, J S Tuttle, R J Oakey, et al.Annales De Genetique|January 1, 1983
[Prenatal diagnosis of a male fetal carrier of fragile X chromosome by the amniotic fluid cells]I Tejada, J Boué, S GilgenkrantzArchives Francaises De Pediatrie|November 1, 1975
[Cat eye syndrome with pituitary dwarfism and normal mental development]M Pierson, S Gilgenkrantz, M SaborioAmerican Journal of Medical Genetics|August 15, 1994
Additional case of female monozygotic twins discordant for the clinical manifestations of Duchenne muscular dystrophy due to opposite X-chromosome inactivationN Abbadi, C Philippe, M Chery, et al.Comptes Rendus Des Seances De La Societe De Biologie Et De Ses Filiales|January 1, 1976
[Action of 5-bromodeoxyuridine as a function of time on the aspect of chromosomes. Attempt at interpretation]S Gilgenkrantz, M J Gregoire, F StreiffBulletin De L'Association Des Anatomistes|June 1, 1976
[Cytogenetic studies in spontaneous abortions]S Gilgenkrantz, M J Gregoire, F StreiffHuman Molecular Genetics|July 1, 1994
Cloning and characterization of the human choroideremia geneH van Bokhoven, J A van den Hurk, L Bogerd, et al.Pageof 24