Hallazgos clínicos y genéticos de dos casos con síndrome de Apert-Reference-Cited by-同舟云学术

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Hallazgos clínicos y genéticos de dos casos con síndrome de Apert

Published:2019-07-26 Issue:1 Volume:76 Page:
ISSN:0539-6115
Container-title:Boletín Médico del Hospital Infantil de México
language:es
Short-container-title:BMHIM

Author:

Cammarata-Scalisi Francisco,Yilmaz Elanur,Callea Michele,Avendaño Andrea,Mihçi Ercan,Alper Ozgul M.

Publisher

Publicidad Permanyer, SLU

Subject

Pediatrics, Perinatology and Child Health

Cited by 4 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. Cleft Palate in Apert Syndrome;Journal of Developmental Biology;2022-08-11

2. The Evaluation of FGFR1, FGFR2 and FOXO1 in Orofacial Cleft Tissue;Children;2022-04-06

3. Early Prenatal Ultrasound and Molecular Diagnosis of Apert Syndrome: Case Report with Postmortem CT-Scan and Chondral Plate Histology;Fetal and Pediatric Pathology;2020-06-15

4. Apert Syndrome: Diagnostic and Management Problems in a Resource-Limited Country;Pediatric Reports;2019-12-02

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