Neonatal Pancytopenia Associated With De Novo 1q43-44 Deletion and 10p15 Duplication
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Oncology,Hematology,Pediatrics, Perinatology and Child Health
Reference22 articles.
1. Acute lymphoblastic leukemia in a patient with constitutional chromosome 1pter-p36.31 duplication and 1q43-qter deletion.;Khan;J Pediatr Hematol Oncol,2012
2. Deletion of the distal long arm of chromosome 1: a definable syndrome.;Johnson;Am J Med Genet,1985
3. Clinical and molecular characteristics of 1qter microdeletion syndrome: delineating a critical region for corpus callosum agenesishypogenesis.;van Bon;J Med Genet,2008
4. High-resolution array CGH defines critical regions and candidate genes for microcephaly, abnormalities of the corpus callosum, and seizure phenotypes in patients with microdeletions of 1q43q44.;Ballif;Hum Genet,2012
5. Four patients with speech delay, seizures and variable corpus callosum thickness sharing a 0.440 Mb deletion in region 1q44 containing the HNRPU gene.;Caliebe;Eur J Med Genet,2010
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