[10号染色体长臂末端部分缺失。1例新病例]
[Partial deletion 10qter. A new case].
作者信息
Vanlieferinghen P, Dechelotte P, Charbonné F
机构信息
Unité de Réanimation Néonatale et Infantile Clinique Médicale Infantile A, Clermont-Ferrand.
出版信息
Ann Genet. 1987;30(2):118-21.
PMID:3314664
Abstract
A newborn with 10qter deletion is described and compared with the others previously reported cases. We confirm that the clinical features are not characteristic enough to delineate a syndrome in this chromosomal abnormality.
摘要
本文描述了一名患有10q末端缺失的新生儿，并将其与先前报道的其他病例进行了比较。我们证实，临床特征不足以在这种染色体异常中明确一种综合征。
Zotero 插件