Craniosynostosis in 10q26 deletion patients: A consequence of brain underdevelopment or altered suture biology?-Reference-Cited by-同舟云学术

Craniosynostosis in 10q26 deletion patients: A consequence of brain underdevelopment or altered suture biology?

Published:2015-11-14 Issue:2 Volume:170 Page:403-409
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Faria Ágatha Cristhina¹²,Rabbi-Bortolini Eliete³,Rebouças Maria R. G. O.⁴,de S. Thiago Pereira Andréia L. A.⁵,Frasson Milena G. Tonini⁵,Atique Rodrigo⁶,Lourenço Naila Cristina V.⁶,Rosenberg Carla⁶,Kobayashi Gerson S.⁶,Passos-Bueno Maria Rita⁶,Errera Flávia Imbroisi Valle¹²

Affiliation:

1. Programa de Graduação em Biotecnologia, Centro de Ciências da Saúde; Universidade Federal do Espírito Santo (UFES); Vitória Espírito Santo Brasil

2. Laboratório de Genética Humana e Molecular, Centro de Pesquisa ICALP; Escola Superior de Ciências da Santa Casa de Misericórdia (EMESCAM); Vitória Espírito Santo Brasil

3. Laboratório de Genética e Biologia Molecular; Associação Educacional de Vitória; Vitória Espírito Santo Brasil

4. Divisão de Genética Clínica; Hospital Estadual Infantil Nossa Senhora da Glória (HEINSG); Vitória Espírito Santo Brasil

5. Unidade de Neonatologia; Hospital Santa Casa de Misericórdia; Vitória Espírito Santo Brasil

6. Centro de Pesquisas Sobre o Genoma Humano e Células Tronco, Departamento de Genética e Biologia Evolutiva; Instituto De Biociências, Universidade de São Paulo (USP); São Paulo São Paulo Brasil

Publisher

Wiley

Subject

Genetics(clinical),Genetics

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2. Terminal 10q26.12 deletion is associated with neonatal asymmetric crying facies syndrome: a case report and literature review;Molecular Cytogenetics;2021-07-13

3. WDR11 is another causative gene for coloboma, cardiac anomaly and growth retardation in 10q26 deletion syndrome;European Journal of Medical Genetics;2020-01

4. De novo variants in EBF3 are associated with hypotonia, developmental delay, intellectual disability, and autism;Molecular Case Studies;2017-11

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