Nance–Horan syndrome in females due to a balanced X;1 translocation that disrupts the NHS gene: Familial case report and review of the literature-Reference-Cited by-同舟云学术

Nance–Horan syndrome in females due to a balanced X;1 translocation that disrupts the NHS gene: Familial case report and review of the literature

Published:2017-09-18 Issue:1 Volume:39 Page:56-62
ISSN:1381-6810
Container-title:Ophthalmic Genetics
language:en
Short-container-title:Ophthalmic Genetics

Author:

Gómez-Laguna Laura¹,Martínez-Herrera Alejandro²,Reyes-de la Rosa Alejandra del Pilar³,García-Delgado Constanza³,Nieto-Martínez Karem²,Fernández-Ramírez Fernando¹,Valderrama-Atayupanqui Tania Yanet⁴,Morales-Jiménez Ariadna Berenice³,Villa-Morales Judith³,Kofman Susana¹,Cervantes Alicia¹²,Morán-Barroso Verónica Fabiola³

Affiliation:

1. Service of Genetics, Hospital General de México Dr. Eduardo Liceaga, Mexico City, Mexico

2. Faculty of Medicine, Universidad Nacional Autónoma de México (UNAM), Mexico City, Mexico

3. Department of Genetics, Hospital Infantil de México Federico Gómez, Mexico City, Mexico

4. Department of Ophthalmology, Hospital Infantil de México Federico Gómez, Mexico City, Mexico

Publisher

Informa UK Limited

Subject

Genetics (clinical),Ophthalmology,Pediatrics, Perinatology and Child Health

Link

https://www.tandfonline.com/doi/pdf/10.1080/13816810.2017.1363245

Reference35 articles.

1. The Nance-Horan syndrome.

2. Mental retardation in Nance-Horan syndrome: Clinical and neuropsychological assessment in four families

3. A Turkish family with Nance-Horan syndrome due to a novel mutation

4. Nance-Horan syndrome: linkage analysis in 4 families refines localization in Xp22.31-p22.13 region

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