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22q13.3 deletion syndrome: clinical and molecular analysis using array CGH.
Dhar, S U; del Gaudio, D; German, J R; Peters, S U; Ou, Z; Bader, P I; Berg, J S; Blazo, M; Brown, C W; Graham, B H; Grebe, T A; Lalani, S; Irons, M; Sparagana, S; Williams, M; Phillips, J A; Beaudet, A L; Stankiewicz, P; Patel, A; Cheung, S W; Sahoo, T.
Affiliation
  • Dhar SU; Department of Molecular & Human Genetics, Baylor College of Medicine, Houston, Texas 77030, USA.
Am J Med Genet A ; 152A(3): 573-81, 2010 Mar.
Article in En | MEDLINE | ID: mdl-20186804
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Chromosomes, Human, Pair 22 / Chromosome Deletion Type of study: Prognostic_studies Limits: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male Language: En Journal: Am J Med Genet A Journal subject: GENETICA MEDICA Year: 2010 Document type: Article Affiliation country: Estados Unidos Country of publication: Estados Unidos
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Chromosomes, Human, Pair 22 / Chromosome Deletion Type of study: Prognostic_studies Limits: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male Language: En Journal: Am J Med Genet A Journal subject: GENETICA MEDICA Year: 2010 Document type: Article Affiliation country: Estados Unidos Country of publication: Estados Unidos