Two children with subtelomeric 11q deletions: a description and interpretation of their clinical presentations and molecular genetic findings-Reference-Cited by-同舟云学术

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Two children with subtelomeric 11q deletions: a description and interpretation of their clinical presentations and molecular genetic findings

Published:2009-04 Issue:2 Volume:18 Page:98-102
ISSN:0962-8827
Container-title:Clinical Dysmorphology
language:en
Short-container-title:

Author:

Cox Helen,Lucassen Anneke,Rio Marlene,Browne Caroline,Renforth Glenn,Craven Lyndsey,Salmon Tony,Wilson David I.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Genetics(clinical),General Medicine,Pathology and Forensic Medicine,Anatomy,Pediatrics, Perinatology, and Child Health

Reference25 articles.

1. A new congenital dysmegakaryopoetic thrombocytopenia (Paris-Trousseau) associated with giant platelet α-granules and chromosome 11 deletion at 11q23;Breton-Gorius;Blood,1995

2. Detecting rearrangements in children using FISH and SKY;Clarkson;Am J Med Genet,2002

3. A boy with a sub microscopic 22qter deletion, general overgrowth and features suggestive of FG syndrome;De Vries;Clin Genet,2000

4. Sub microscopic subtelomeric 1qter deletions: a recognisable phenotype?;De Vries;J Med Genet,2001a

5. Clinical studies on sub microscopic subtelomeric rearrangements: a checklist;De Vries;J Med Genet,2001b

Cited by 2 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. Cognitive-behavioral characteristics and developmental trajectories in children with deletion 11qter (Jacobsen syndrome), and their relation to deletion size;American Journal of Medical Genetics Part A;2014-11-25

2. Partial Trisomy 3p and Partial Monosomy 11q Associated with Atrial Septal Defect, Cleft Palate, and Developmental Delay: A Case Report;Cytogenetic and Genome Research;2011

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