Inherited Xq13.2-q21.31 duplication in a boy with recurrent seizures and pubertal gynecomastia: Clinical, chromosomal and aCGH characterization-Reference-Cited by-同舟云学术

Inherited Xq13.2-q21.31 duplication in a boy with recurrent seizures and pubertal gynecomastia: Clinical, chromosomal and aCGH characterization

Published:2016-09 Issue: Volume:9 Page:185-190
ISSN:2214-5400
Container-title:Meta Gene
language:en
Short-container-title:Meta Gene

Author:

Linhares Natália D.,Valadares Eugênia R.,da Costa Silvia S.,Arantes Rodrigo R.,de Oliveira Luiz Roberto,Rosenberg Carla,Vianna-Morgante Angela M.,Svartman Marta

Funder

FAPEMIG

FAPESP

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference23 articles.

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3. Neurodevelopmental defects resulting from ATRX overexpression in transgenic mice;Berube;Hum. Mol. Genet.,2002

4. Conservation of PCDHX in mammals; expression of human X/Y genes predominantly in brain;Blanco;Mamm. Genome,2000

5. Mental retardation, distinct facial changes, short stature, obesity, and hypogonadism: a new X-linked mental retardation syndrome;Chudley;Am. J. Med. Genet.,1988

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