Autosomal dominant oculoauriculovertebral spectrum and 14q23.1 microduplication-Reference-Cited by-同舟云学术

Autosomal dominant oculoauriculovertebral spectrum and 14q23.1 microduplication

Published:2013-06-21 Issue:8 Volume:161 Page:2030-2035
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Ballesta-Martínez Maria Juliana¹,López-González Vanesa¹,Dulcet Lluis Armengol²,Rodríguez-Santiago Benjamín²,Garcia-Miñaúr Sixto³,Guillen-Navarro Encarna¹

Affiliation:

1. Unidad de Genética Médica y Dismorfología, Servicio de Pediatría, Hospital Universitario Virgen de la Arrixaca; Murcia; Spain

2. Quantitative Genomic Medicine Laboratories; Barcelona; Spain

3. Instituto de Genética Médica y Molecular-INGEMM, Hospital Universitario La Paz; Madrid; Spain

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.36007/fullpdf

Reference24 articles.

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3. Congenital heart defects in patients with oculo-auriculo-vertebral spectrum (Goldenhar syndrome);Digilio;Am J Med Genet Part A,2008

4. Oculovertebralauricular Dysplasia;Gorlin;J Pediatr,1963

5. Review of the etiologic heterogeneity of the oculo-auriculo-vertebral spectrum (Hemifacial Microsomia);Hartsfield;Orthod Craniofac Res,2007

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