两例Apert综合征的临床与遗传学分析

IF 0.6 Q4 PEDIATRICS
Francisco Cammarata-Scalisi, Elanur Yilmaz, Michele Callea, Andrea Avendaño, Ercan Mihçi, Ozgul M. Alper
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引用次数: 2

摘要

本文章由计算机程序翻译,如有差异,请以英文原文为准。
Clinical and genetic findings of two cases with Apert syndrome
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来源期刊
CiteScore
1.60
自引率
0.00%
发文量
73
审稿时长
20 weeks
期刊介绍: The Boletín Médico del Hospital Infantil de México is a bimonthly publication edited by the Hospital Infantil de México Federico Gómez. It receives unpublished manuscripts, in English or Spanish, relating to paediatrics in the following areas: biomedicine, clinical, public health, clinical epidemology, health education and clinical ethics. Articles can be original research articles, in-depth or systematic reviews, clinical cases, clinical-pathological cases, articles about public health, letters to the editor or editorials (by invitation).
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