Microduplications of 3p26.3p26.2 containing CRBN gene in patients with intellectual disability and behavior abnormalities-Reference-Cited by-同舟云学术

Microduplications of 3p26.3p26.2 containing CRBN gene in patients with intellectual disability and behavior abnormalities

Published:2015-05 Issue:5 Volume:58 Page:319-323
ISSN:1769-7212
Container-title:European Journal of Medical Genetics
language:en
Short-container-title:European Journal of Medical Genetics

Author:

Papuc Sorina M.,Hackmann Karl,Andrieux Joris,Vincent-Delorme Catherine,Budişteanu Magdalena,Arghir Aurora,Schrock Evelin,Ţuţulan-Cuniţă Andreea C.,Di Donato Nataliya

Funder

Wellcome Trust

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics,General Medicine

Reference25 articles.

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2. A 9-year-old male with a duplication of chromosome 3p25.3p26.2: clinical report and gene expression analysis;Bittel;Am J Med Genet,2006

3. Clinical and cytogenetic spectrum of duplication 3p;Braga;Eur J Pediatr,1982

4. Recurrent reciprocal 1q21.1 deletions and duplications associated with microcephaly or macrocephaly and developmental and behavioral abnormalities;Brunetti-Pierri;Nat Genet,2008

5. Molecular cytogenetic characterization of a subtle interstitial del(3)(p25.3p26.2) in a patient with deletion 3p syndrome;Cargile;Am J Med Genet,2002

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