De novo 911 Kb interstitial deletion on chromosome 1q43 in a boy with mental retardation and short stature
Author:
Publisher
Elsevier BV
Subject
Genetics (clinical),Genetics,General Medicine
Reference12 articles.
1. Terminal (1)(q43) long-arm deletion of chromosome no. 1 in a three-year-old female;Mankinen;Birth Defects Orig. Artic. Ser.,1976
2. Two new cases of pure 1q terminal deletion presenting with brain malformations;Hiraki;Am. J. Med. Genet. Part A,2008
3. A 2-Mb critical region implicated in the microcephaly associated with terminal 1q deletion syndrome;Hill;Am. J. Med. Genet. A,2007
4. Formin-dependent synaptic growth: evidence that dlar signals via Diaphanous to modulate synaptic actin and dynamic pioneer microtubules;Pawson;J. Neurosci.,2008
5. Formin-2, a novel forming homology protein of the cappuccino subfamily, is highly expressed in the developing and adult central nervous system;Leader;Mech. Develop.,2000
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