Literature DB >> 9809264

Developmental presentation of 22q11.2 deletion (DiGeorge/velocardiofacial syndrome).

P P Wang1, C Solot, E M Moss, M Gerdes, D M McDonald-McGinn, D A Driscoll, B S Emanuel, E H Zackai.   

Abstract

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Year:  1998        PMID： 9809264     DOI： 10.1097/00004703-199810000-00004

Source DB:  PubMed          Journal:  J Dev Behav Pediatr        ISSN： 0196-206X            Impact factor:   2.225


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  5 in total

1.  Rare copy number variants in tourette syndrome disrupt genes in histaminergic pathways and overlap with autism.

Authors:  Thomas V Fernandez; Stephan J Sanders; Ilana R Yurkiewicz; A Gulhan Ercan-Sencicek; Young-Shin Kim; Daniel O Fishman; Melanie J Raubeson; Youeun Song; Katsuhito Yasuno; Winson S C Ho; Kaya Bilguvar; Joseph Glessner; Su Hee Chu; James F Leckman; Robert A King; Donald L Gilbert; Gary A Heiman; Jay A Tischfield; Pieter J Hoekstra; Bernie Devlin; Hakon Hakonarson; Shrikant M Mane; Murat Günel; Matthew W State
Journal:  Biol Psychiatry       Date:  2011-12-14       Impact factor: 13.382

2.  Behavior, brain, and genome in genomic disorders: finding the correspondences.

Authors:  Elena L Grigorenko; Alexander E Urban; Einar Mencl
Journal:  J Dev Behav Pediatr       Date:  2010-09       Impact factor: 2.225

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

Review 4.  Genetics of Cleft Palate and Velopharyngeal Insufficiency.

Authors:  Walter M Sweeney; Steve T Lanier; Chad A Purnell; Arun K Gosain
Journal:  J Pediatr Genet       Date:  2015-03

5.  Factors affecting articulation skills in children with velocardiofacial syndrome and children with cleft palate or velopharyngeal dysfunction: a preliminary report.

Authors:  Adriane L Baylis; Benjamin Munson; Karlind T Moller
Journal:  Cleft Palate Craniofac J       Date:  2008-03
  5 in total

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