Incidental Radiologic Findings in the 22q11.2 Deletion Syndrome-Reference-Cited by-同舟云学术

Incidental Radiologic Findings in the 22q11.2 Deletion Syndrome

Published:2014-06-19 Issue:11 Volume:35 Page:2186-2191
ISSN:0195-6108
Container-title:American Journal of Neuroradiology
language:en
Short-container-title:AJNR Am J Neuroradiol

Author:

Schmitt J.E.,Yi J.J.,Roalf D.R.,Loevner L.A.,Ruparel K.,Whinna D.,Souders M.C.,McDonald-McGinn D.M.,Yodh E.,Vandekar S.,Zackai E.H.,Gur R.C.,Emanuel B.S.,Gur R.E.

Publisher

American Society of Neuroradiology (ASNR)

Subject

Clinical Neurology,Radiology Nuclear Medicine and imaging

Reference53 articles.

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2. Prevalence of 22q11 microdeletions in DiGeorge and velocardiofacial syndromes: implications for genetic counselling and prenatal diagnosis.

3. Low-Copy Repeats Mediate the Common 3-Mb Deletion in Patients with Velo-cardio-facial Syndrome

4. Chromosome 22-specific low copy repeats and the 22q11.2 deletion syndrome: genomic organization and deletion endpoint analysis

5. Bridging the gene–behavior divide through neuroimaging deletion syndromes: Velocardiofacial (22q11.2 Deletion) and Williams (7q11.23 Deletion) syndromes

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