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Clinical and molecular characterization of the 20q11.2 microdeletion syndrome: six new patients.
Jedraszak, Guillaume; Demeer, Bénédicte; Mathieu-Dramard, Michèle; Andrieux, Joris; Receveur, Aline; Weber, Astrid; Maye, Una; Foulds, Nicola; Temple, I K; Crolla, John; Alex-Cordier, Marie-Pierre; Sanlaville, Damien; Ewans, Lisa; Wilson, Meredith; Armstrong, Ruth; Clarkson, Amanda; Copin, Henri; Morin, Gilles.
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  • Jedraszak G; Unité de Génétique Médicale et Oncogénétique, Centre Hospitalier Universitaire Amiens Picardie, Amiens, France; Laboratoire de Cytogénétique et Biologie de la Reproduction, Centre Hospitalier Universitaire Amiens Picardie, Amiens, France.
Am J Med Genet A ; 167A(3): 504-11, 2015 Mar.
Article in En | MEDLINE | ID: mdl-25572454
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Phenotype / Abnormalities, Multiple / Chromosomes, Human, Pair 20 / Chromosome Deletion Type of study: Prognostic_studies Limits: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male Language: En Journal: Am J Med Genet A Journal subject: GENETICA MEDICA Year: 2015 Document type: Article Affiliation country: Francia
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Phenotype / Abnormalities, Multiple / Chromosomes, Human, Pair 20 / Chromosome Deletion Type of study: Prognostic_studies Limits: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male Language: En Journal: Am J Med Genet A Journal subject: GENETICA MEDICA Year: 2015 Document type: Article Affiliation country: Francia