SNP array and phenotype correlation shows that FLI1 deletion per se is not responsible for thrombocytopenia development in Jacobsen syndrome-Reference-Cited by-同舟云学术

SNP array and phenotype correlation shows that FLI1 deletion per se is not responsible for thrombocytopenia development in Jacobsen syndrome

Published:2012-08-07 Issue:10 Volume:158A Page:2545-2550
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Trkova Marie,Becvarova Vera,Hynek Martin,Hnykova Lenka,Hlavova Eva,Kreckova Gabriela,Kulovany Eduard,Cutka David,Zatloukalova Jitka,Markova Kristyna,Sukova Martina,Horacek Jiri,Stejskal David

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference27 articles.

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4. Cytomegalovirus infection in pregnancy: Should all women be screened?;Carlson;Rev Obstet Gynecol,2010

5. Prenatal diagnosis of the distal 11q deletion and review of the literature;Chen;Prenat Diagn,2004

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3. Transcription factor defects causing platelet disorders;Blood Reviews;2017-01

4. Complex Mosaic Ring Chromosome 11 Associated with Hemizygous Loss of 8.6 Mb of 11q24.2qter in Atypical Jacobsen Syndrome;Molecular Syndromology;2016-11-17

5. Jacobsen Syndrome: Surgical Complications due to Unsuspected Diagnosis, the Importance of Molecular Studies in Patients with Craniosynostosis;Molecular Syndromology;2015-12-18