First molecular-cytogenetic characterization of Fanconi anemia fragile sites in primary lymphocytes of FA-D2 patients in different stages of the disease-Reference-Cited by-同舟云学术

First molecular-cytogenetic characterization of Fanconi anemia fragile sites in primary lymphocytes of FA-D2 patients in different stages of the disease

Published:2016-09-13 Issue:1 Volume:9 Page:
ISSN:1755-8166
Container-title:Molecular Cytogenetics
language:en
Short-container-title:Mol Cytogenet

Author:

Filipović Jelena,Joksić Gordana,Vujić Dragana,Joksić Ivana,Mrasek Kristin,Weise Anja,Liehr Thomas

Funder

Ministarstvo Prosvete, Nauke i Tehnolokog Razvoja

DAAD

Publisher

Springer Science and Business Media LLC

Subject

Biochemistry (medical),Genetics (clinical),Genetics,Molecular Biology,Molecular Medicine,Biochemistry

Link

http://link.springer.com/content/pdf/10.1186/s13039-016-0280-6.pdf

Reference40 articles.

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3. Vujic D, Petrovic S, Lazic E, Kuzmanovic M, Leskovac A, Joksic I, Micic D, Jovanovic A, Zecevic Z, Guc-Scekic M, Cirkovic S, Joksic G. Prevalence of FA-D2 Rare Complementation Group of Fanconi Anemia in Serbia. Indian J Pediatr. 2014;81:260–5.

4. Whitney M, Thayer M, Reifsteck C, Olson S, Smith L, Jakobs P, Leach R, Naylor S, Joenje H, Grompe M. Microcell mediated chromosome transfer maps the Fanconi anaemia group D gene to chromosome 3p. Nat Genet. 1995;11:341–3.

5. Kalb R, Neveling K, Hoehn H, Schneider H, Linka Y, Batish SD, Hunt C, Berwick M, Callen E, Surralles J, Casado JA, Bueren J, Dasi A, Soulier J, Gluckman E, Zwaan CM, van Spaendonk R, Pals G, de Winter JP, Joenje H, Grompe M, Auerbach AD, Hanenberg H, Schindler D. Hypomorphic mutations in the gene encoding a key Fanconi anemia protein, FANCD2, sustain a significant group of FA-D2 patients with severe phenotype. Am J Hum Genet. 2007;80:895–910.

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