PartialAFF2microduplication in a patient with auditory processing disorder, emotional impairment and macrosomia-Reference-Cited by-同舟云学术

PartialAFF2microduplication in a patient with auditory processing disorder, emotional impairment and macrosomia

Published:2014-09-24 Issue:12 Volume:164 Page:3206-3208
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

da Rocha Naiara Braz¹,dos Santos Pollyanna Almeida Costa¹,Safatle Heloisa Pires Netto²,de Melo Reneide Maria³,Pereira Rinaldo Wellerson⁴,de Oliveira Silviene Fabiana⁵⁶,Pic-Taylor Aline⁵,Ferrari Iris²⁵,Mazzeu Juliana Forte¹⁴

Affiliation:

1. Programa de Pós-graduação em Ciências da Saúde; Universidade de Brasília; DF Brazil

2. Hospital Universitário; Universidade de Brasília; Brasília DF Brazil

3. CIAPE; Gama DF Brazil

4. Programa de Pós-Graduação em Ciências Genômicas e Biotecnologia; Universidade Católica de Brasília; Brasília DF Brazil

5. Laboratório de Genética; Departamento de Genética e Morfologia; Instituto de Ciências Biológicas. Universidade de Brasília; Brasília DF Brazil

6. Jackson Laboratory for Genomic Medicine; Farmington Connecticut

Funder

CNPq

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.36768/fullpdf

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3. severe hunter syndrome (Mucopolysaccharidosis II) phenotype secondary to large deletion in the X chromosome encompassing IDS, FMR1, and AFF2 (FMR2);Burruss;J Child Neurol,2011

4. expression of the murine homologue of FMR2 in mouse brain and during development;Chakrabarti;Hum Mol Genet,1998

5. A candidate gene for mild mental handicap at the FRAXE fragile site;Chakrabarti;Hum Mol Genet,1996

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