Showing results (1-10 of 71) with videos related to

Sort By:
Pageof 8
Cancer Genetics and Cytogenetics|June 20, 2002
Compilation of published comparative genomic hybridization studiesStéphanie Struski, Martine Doco-Fenzy, Pascale Cornillet-Lefebvre
Methods in Molecular Biology (Clifton, N.J.)|August 30, 2025
ISCN and ChromoanagenesisMartine Doco-Fenzy, Jean-Michel Dupont, Caroline Schluth-Bolard
European Journal of Medical Genetics|November 12, 2021
Hepatotoxicity of metronidazole in Cockayne syndrome: A clinical reportThomas Hunaut, Camille Boulagnon-Rombi, Hugo Thorn, et al.
The British Journal of Oral & Maxillofacial Surgery|December 14, 2011
Cleft palate and bilateral congenital cataract: a familial observation: a new syndrome?Caroline François-Fiquet, Olivier Wavreille, Marie-Laurence Poli Merol, et al.
American Journal of Medical Genetics. Part A|January 13, 2021
Adult diagnosis of Townes-Brocks syndrome with renal failure: Two related cases and review of literatureOlivia Beaudoux, Anne-Sophie Lebre, Martine Doco Fenzy, et al.
Pathology, Research and Practice|February 16, 2008
Collapsing glomerulopathy in Galloway-Mowat syndrome: a case report and review of the literatureHervé Sartelet, Christine Pietrement, Laure-Hélène Noel, et al.
Cancer Genetics and Cytogenetics|January 22, 2002
Cytogenetic characterization of chromosomal rearrangement in a human vinblastine-resistant CEM cell line: use of comparative genomic hybridization and fluorescence in situ hybridizationStephanie Struski, Pascale Cornillet-Lefebvre, Martine Doco-Fenzy, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|March 26, 2013
Sirenomelia: a new type, showing VACTERL association with Thomas syndrome and a review of literatureMartin Lhuaire, Agnès Jestin, Camille Boulagnon, et al.
European Journal of Medical Genetics|December 15, 2010
A 5.3Mb deletion in chromosome 18q12.3 as the smallest region of overlap in two patients with expressive speech delaySonia Bouquillon, Joris Andrieux, Emilie Landais, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|December 12, 2018
Genetics of Usher Syndrome: New Insights From a Meta-analysisGuillaume Jouret, Céline Poirsier, Marta Spodenkiewicz, et al.
Pageof 8