In the line-up: deleted genes associated with DiGeorge/22q11.2 deletion syndrome: are they all suspects?-Reference-Cited by-同舟云学术

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In the line-up: deleted genes associated with DiGeorge/22q11.2 deletion syndrome: are they all suspects?

Published:2019-06-07 Issue:1 Volume:11 Page:
ISSN:1866-1947
Container-title:Journal of Neurodevelopmental Disorders
language:en
Short-container-title:J Neurodevelop Disord

Author:

Motahari Zahra,Moody Sally Ann,Maynard Thomas Michael,LaMantia Anthony-Samuel

Funder

National Institute of Child Health and Human Development

Eunice Kennedy Shriver National Institute of Child Health and Human Development

Simons Foundation

Publisher

Springer Science and Business Media LLC

Subject

Cognitive Neuroscience,Neurology (clinical),Pathology and Forensic Medicine,Pediatrics, Perinatology and Child Health

Link

http://link.springer.com/content/pdf/10.1186/s11689-019-9267-z.pdf

Reference418 articles.

1. McDonald-McGinn DM, Sullivan KE. Chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/ velocardiofacial syndrome). Medicine (Baltimore). 2011;90(1):1–18.

2. Burn J, Takao A, Wilson D, Cross I, Momma K, Wadey R, Scambler P, Goodship J. Conotruncal anomaly face syndrome is associated with a deletion within chromosome 22q11. J Med Genet. 1993;30(10):822–4.

3. Fernandez A, Meechan D, Baker JL, Karpinski BA, LaMantia AS, Maynard TM. 22q11 deletion syndrome: copy number variations and development. In: Principles of Developmental Genetics. 2nd ed; 2015. p. 677–96.

4. Robin NH, Shprintzen RJ. Defining the clinical spectrum of deletion 22q11.2. J Pediatr. 2005;147(1):90–6.

5. Schneider M, Debbane M, Bassett AS, Chow EW, Fung WL, van den Bree M, et al. Psychiatric disorders from childhood to adulthood in 22q11.2 deletion syndrome: results from the international consortium on brain and behavior in 22q11.2 deletion syndrome. Am J Psychiatry. 2014;171(6):627–39.

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