Literature DB >> 9603617

On cognitive variability in velocardiofacial syndrome: profound mental retardation and autism.

C Kozma.   

Abstract

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Mesh：

Year:  1998        PMID： 9603617     DOI： 10.1002/(sici)1096-8628(19980508)81:3<269::aid-ajmg12>3.0.co;2-d

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN： 0148-7299


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  4 in total

1.  The use of two different MLPA kits in 22q11.2 deletion syndrome.

Authors:  L J M Evers; J J M Engelen; L M H Houben; L M G Curfs; T A M J van Amelsvoort
Journal:  Eur J Med Genet       Date:  2016-02-24       Impact factor: 2.708

2.  Autism spectrum disorders and symptoms in children with molecularly confirmed 22q11.2 deletion syndrome.

Authors:  Sarah E Fine; Alison Weissman; Marsha Gerdes; Jennifer Pinto-Martin; Elaine H Zackai; Donna M McDonald-McGinn; Beverly S Emanuel
Journal:  J Autism Dev Disord       Date:  2005-08

Review 3.  Phenotype of adults with the 22q11 deletion syndrome: A review.

Authors:  E Cohen; E W Chow; R Weksberg; A S Bassett
Journal:  Am J Med Genet       Date:  1999-10-08

4.  An Adult Case of Chromosome 22q11.2 Deletion Syndrome Associated with a High-positioned Right Aortic Arch.

Authors:  Yoichi Hoshino; Moriya Machida; Shun-Ichi Shimano; Teizo Taya
Journal:  Intern Med       Date:  2017-04-01       Impact factor: 1.271
  4 in total

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