Platelet parameters in children with chromosome 22q11 deletion and conotruncal heart defects-Reference-Cited by-同舟云学术

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Platelet parameters in children with chromosome 22q11 deletion and conotruncal heart defects

Published:2018-03-05 Issue:3 Volume:13 Page:483-487
ISSN:1747-079X
Container-title:Congenital Heart Disease
language:en
Short-container-title:Congenital Heart Disease

Author:

Anilkumar Alka¹^ORCID,Vasudevan D. M.²,Kappanayil Mahesh³,Sundaram K. R.⁴,Krishna Kumar R.³,Nampoothiri Sheela⁵

Affiliation:

1. Department of Human Cytogenetics; Amrita Institute of Medical Sciences and Research Centre; Kochi India

2. School of Medicine; Amrita Institute of Medical Sciences and Research Centre; Kochi India

3. Department of Paediatric Cardiology; Amrita Institute of Medical Sciences and Research Centre; Kochi India

4. Department of Biostatistics; Amrita Institute of Medical Sciences and Research Centre; Kochi India

5. Department of Paediatric Genetics; Amrita Institute of Medical Sciences and Research Centre; Kochi India

Funder

Indian Council of Medical Research

Publisher

Computers, Materials and Continua (Tech Science Press)

Subject

Cardiology and Cardiovascular Medicine,Radiology Nuclear Medicine and imaging,General Medicine,Surgery,Pediatrics, Perinatology, and Child Health

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/chd.12600/fullpdf

Reference27 articles.

1. Velo-cardio-facial syndrome: a distinctive behavioural phenotype;Shprintzen;Ment Retard Dev Disabil Res Rev.,2000

2. 22q11.2 deletions in patients with conotruncal defects: data from 1,610 consecutive cases;Peyvandi;Pediatr Cardiol.,2013

3. Association of schizophrenia in 22q11.2 deletion syndrome and gray matter volumetric deficits in the superior temporal gyrus;Chow;Am J Psychiatr.,2011

4. Variation in prevalence of chromosome 22q11 deletion in subtypes of conotruncal defect in 254 children;Anilkumar;Acta Paediatr.,2011

5. Cognitive, behavioural, and psychiatric phenotype in 22q11.2 deletion syndrome;Philip;Behav Genet.,2011

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Hemizygosity for the gene encoding glycoprotein Ibβ is not responsible for macrothrombocytopenia and bleeding in patients with 22q11 deletion syndrome;Journal of Thrombosis and Haemostasis;2019-01-22

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