Thrombocytopenia in patients with 22q11.2 deletion syndrome and its association with glycoprotein Ib-β-Reference-Cited by-同舟云学术

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Thrombocytopenia in patients with 22q11.2 deletion syndrome and its association with glycoprotein Ib-β

Published:2003-03 Issue:2 Volume:5 Page:113-119
ISSN:1098-3600
Container-title:Genetics in Medicine
language:en
Short-container-title:Genetics in Medicine

Author:

Kato Taichi,Kosaka Kazuki,Kimura Misa,Imamura Shin-ichiro,Yamada Osamu,Iwai Kazumasa,Ando Masahiko,Joh-o Kunitaka,Kuroe Kenji,Ohtake Akira,Takao Atsuyoshi,Momma Kazuo,Matsuoka Rumiko

Publisher

Elsevier BV

Subject

Genetics (clinical)

Reference35 articles.

1. A new concept of the cellular basis of immunity

2. A deletion in chromosome 22 can cause digeorge syndrome

3. Conotruncal anomaly face syndrome is associated with a deletion within chromosome 22q11.

4. Confirmation that the conotruncal anomaly face syndrome is associated with a deletion within 22q11.2

Cited by 44 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. A Case of Bernard-Soulier Syndrome Associated with 22q11.2 Deletion Syndrome;Clinical Pediatric Hematology-Oncology;2023-10-31

2. Childhood manifestations of 22q11.2 deletion syndrome: A Finnish nationwide register‐based cohort study;Acta Paediatrica;2023-03-07

3. Updated clinical practice recommendations for managing adults with 22q11.2 deletion syndrome;Genetics in Medicine;2023-03

4. 22q11.2 Deletion Syndrome: Impact of Genetics in the Treatment of Conotruncal Heart Defects;Children;2022-05-25

5. Hematologic and oncological manifestations of 22q11.2 deletion syndrome;The Chromosome 22q11.2 Deletion Syndrome;2022

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