Prevalence of FA-D2 Rare Complementation Group of Fanconi Anemia in Serbia-Reference-Cited by-同舟云学术

Prevalence of FA-D2 Rare Complementation Group of Fanconi Anemia in Serbia

Published:2013-12-10 Issue:3 Volume:81 Page:260-265
ISSN:0019-5456
Container-title:The Indian Journal of Pediatrics
language:en
Short-container-title:Indian J Pediatr

Author:

Dragana Vujić,Sandra Petrović,Emilija Lazić,Miloš Kuzmanović,Andreja Leskovac,Ivana Joksić,Dragan Mićić,Ankica Jovanović,Željko Zečević,Marija Guć-Šćekić,Sanja Ćirković,Gordana Joksić

Publisher

Springer Science and Business Media LLC

Subject

Pediatrics, Perinatology and Child Health

Link

http://link.springer.com/content/pdf/10.1007/s12098-013-1284-4.pdf

Reference17 articles.

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3. Al-Haggar M, Al-Morsy Z, Yahia S, Chalaby N, Ragab A, Mesbah A. Correlation of thyroid and growth hormones to chromosomal instability in Egyptian Fanconi anemia patients. Indian J Pediatr. 2008;75:679–84.

4. D'Souza F, Usha MK, Subba Rao SD. Fanconi's anemia in monozygotic twins. Indian J Pediatr. 2007;74:859–61.

5. Buchwald M. Complementation groups: One or more per gene? Nat Genet. 1995;11:228–30.

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1. Genotype-phenotype associations in Fanconi anemia: A literature review;Blood Reviews;2019-09

2. Genotyping Fanconi anemia patients from Serbia reveals three novel FANCD2 variants;Genetika;2017

3. First molecular-cytogenetic characterization of Fanconi anemia fragile sites in primary lymphocytes of FA-D2 patients in different stages of the disease;Molecular Cytogenetics;2016-09-13