[A case of a syndrome characterized by short stature, and developmental delay caused by heterozygous variation in the FOXP4 gene].

Subjects

Subjects :

Child
Humans
Male
Body Height
Dwarfism genetics
Growth Disorders genetics
Language Development Disorders genetics
Mutation
Phenotype
Syndrome
Developmental Disabilities genetics
Forkhead Transcription Factors genetics
Heterozygote

Details

Language :

Chinese

ISSN :

0578-1310

Volume :

62

Issue :

6

Database :

MEDLINE

Journal :

Zhonghua er ke za zhi = Chinese journal of pediatrics

Publication Type :

Academic Journal

Accession number :

38763881

Full Text :

https://doi.org/10.3760/cma.j.cn112140-20231117-00379