Unique association of hypochondroplasia with craniosynostosis and cleft palate in a Mexican family-Reference-Cited by-同舟云学术

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Unique association of hypochondroplasia with craniosynostosis and cleft palate in a Mexican family

Published:2017-11-17 Issue:1 Volume:176 Page:161-166
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am J Med Genet

Author:

González-del Angel Ariadna¹^ORCID,Caro-Contreras Alan²,Alcántara-Ortigoza Miguel Angel¹,Ramos Sandra³,Cruz-Alcívar Roberto⁴,Moyers-Pérez Paola⁵

Affiliation:

1. Laboratorio de Biología Molecular, Departamento de Genética Humana; Instituto Nacional de Pediatría; Ciudad de México México

2. Médico Residente de Genética Médica, Departamento de Genética Humana; Instituto Nacional de Pediatría; Ciudad de México México

3. Laboratorio de Citogenética, Departamento de Genética Humana; Instituto Nacional de Pediatría; Ciudad de México México

4. Laboratorio de Genética y Cáncer, Departamento de Genética Humana; Instituto Nacional de Pediatría; Ciudad de México México

5. Hospital Bité-Médica Santa Fe; Ciudad de México; México

Funder

Instituto Nacional de Pediatría (México)

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference31 articles.

1. Association of achondroplasia with sagittal synostosis and scaphocephaly in two patients, an underestimated condition;Accogli;American Journal of Medical Genetics Part A,2015

2. The palatal and oral manifestations of muenke syndrome (FGFR3 related craniosynostosis);Agochukwu;The Journal of Craniofacial Surgery,2012

3. Achondroplasia and multiple-suture craniosynostosis;Albino;The Journal of Craniofacial Surgery,2015

4. Muencke syndrome with cleft lip and palate;Anderson;The Journal of Craniofacial Surgery,2013

5. Molecularly proven hypochondroplasia with cloverleaf skull deformity: A novel association;Angle;Clinical Genetics,1998

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. CLARITY : Co‐occurrences in achondroplasia—craniosynostosis, seizures, and decreased risk of diabetes mellitus;American Journal of Medical Genetics Part A;2021-01-26

2. Genetics and signaling mechanisms of orofacial clefts;Birth Defects Research;2020-07-15

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