39 - EXPLORANDO LA DIVERSIDAD FENOTÍPICA Y GENOTÍPICA DEL SÍNDROME DE MICRODELECIÓN 1P36

IF 2.3 4区医学 Q2 MEDICINE, GENERAL & INTERNAL

Revista clinica espanola Pub Date : 2024-10-01 DOI:10.1016/S0014-2565(24)00294-7

Álex García Tellado, Mónica García Castro, Nuria Puente Ruiz, Sandra de la Roz Fernández, José Luis Fernández Luna, Andrea Sariego Jamargo, José Antonio Riancho Moral

引用次数: 0

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39 -探索1P36微解综合征的表现型和基因型多样性

本文章由计算机程序翻译，如有差异，请以英文原文为准。

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来源期刊

Revista clinica espanola 医学-医学：内科

CiteScore

4.40

自引率

6.90%

发文量

审稿时长

28 days

期刊介绍： Revista Clínica Española published its first issue in 1940 and is the body of expression of the Spanish Society of Internal Medicine (SEMI). The journal fully endorses the goals of updating knowledge and facilitating the acquisition of key developments in internal medicine applied to clinical practice. Revista Clínica Española is subject to a thorough double blind review of the received articles written in Spanish or English. Nine issues are published each year, including mostly originals, reviews and consensus documents.