[A case of Van Wyk-Grumbach syndrome with inherited RET gene variation].

Subjects

Subjects :

Humans
Female
Child
Abnormalities, Multiple genetics
Thyroxine therapeutic use
Hypothyroidism genetics
Hypothyroidism drug therapy
Puberty, Precocious genetics
Mutation
Heterozygote
Proto-Oncogene Proteins c-ret genetics

Details

Language :

Chinese

ISSN :

0578-1310

Volume :

62

Issue :

8

Database :

MEDLINE

Journal :

Zhonghua er ke za zhi = Chinese journal of pediatrics

Publication Type :

Academic Journal

Accession number :

39039885

Full Text :

https://doi.org/10.3760/cma.j.cn112140-20240327-00216