Duplication of the 15q11-q13 region: Clinical and genetic study of 30 new cases-Reference-Cited by-同舟云学术

Duplication of the 15q11-q13 region: Clinical and genetic study of 30 new cases

Published:2014-01 Issue:1 Volume:57 Page:5-14
ISSN:1769-7212
Container-title:European Journal of Medical Genetics
language:en
Short-container-title:European Journal of Medical Genetics

Author:

Al Ageeli Essam,Drunat Séverine,Delanoë Catherine,Perrin Laurence,Baumann Clarisse,Capri Yline,Fabre-Teste Jennifer,Aboura Azzedine,Dupont Céline,Auvin Stéphane,El Khattabi Laila,Chantereau Dominique,Moncla Anne,Tabet Anne-Claude,Verloes Alain

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics,General Medicine

Reference50 articles.

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3. High-resolution molecular characterization of 15q11-q13 rearrangements by array comparative genomic hybridization (array CGH) with detection of gene dosage;Wang;Am. J. Hum. Genet.,2004

4. Swedish survey on extra structurally abnormal chromosomes in 39 105 consecutive prenatal diagnoses: prevalence and characterization by fluorescence in situ hybridization;Blennow;Prenat. Diagn.,1994

5. Chromosome 15 anomalies and the Prader–Willi syndrome: cytogenetic analysis;Mattei;Hum. Genet.,1984

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