View in EDS PDF Full Text

一例常染色体显性遗传智力障碍 21 型患者携带 CTCF 突变.

Saved in:
Bibliographic Details
Title: 一例常染色体显性遗传智力障碍 21 型患者携带 CTCF 突变.
Alternate Title: A case of autosomal dominant intellectual disability type 21 with CTCF mutations.
Authors: 丁娟1, 马明圣1 minsaint@aliyun.com
Source: Basic & Clinical Medicine. Dec2025, Vol. 45 Issue 12, p1639-1642. 4p.
Database: Academic Search Ultimate
Description
ISSN:10016325
DOI:10.16352/j.issn.1001-6325.2025.12.1639