Detection of an interstitial 3q21.1-q21.3 deletion in a child with multiple congenital abnormalities, mental retardation, pancytopenia, and myelodysplasia-Reference-Cited by-同舟云学术

Detection of an interstitial 3q21.1-q21.3 deletion in a child with multiple congenital abnormalities, mental retardation, pancytopenia, and myelodysplasia

Published:2009-06 Issue:6 Volume:149A Page:1323-1326
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Callier P.,Faivre L.,Marle N.,Thauvin-Robinet C.,Guy J.,Mosca A.L.,D'Athis P.,Masurel-Paulet A.,Assous D.,Teyssier J.R.,Huet F.,Mugneret F.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.32857/fullpdf

Reference19 articles.

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2. Array-CGH in a series of 30 patients with mental retardation, dysmorphic features, and congenital malformations detected an interstitial 1p22.2-p31.1 deletion in a patient with features overlapping the Goldenhar syndrome;Callier;Am J Med Genet Part A,2008

3. GATA1 in normal and malignant hematopoiesis;Crispino;Semin Cell Dev Biol,2005

4. Telomeres: A diagnosis at the end of the chromosomes;De Vries;J Med Genet,2003

5. The detection of subtelomeric chromosomal rearrangements in idiopathic mental retardation;Flint;Nature Genet,1995

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4. GATA2 Deficiency Due to de Novo Complete Monoallelic Deletion in an Adolescent With Myelodysplasia;Journal of Pediatric Hematology/Oncology;2018-05

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