A Case Report of Familial Mayer-Rokitansky-Küster-Hauser Syndrome as Part of the Phenotypic Spectrum of the 2q37 Deletion.
J Pediatr Adolesc Gynecol
; 37(1): 95-97, 2024 Feb.
Article
in En
| MEDLINE
| ID: mdl-37734585
Key words
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Congenital Abnormalities
/
46, XX Disorders of Sex Development
Type of study:
Prognostic_studies
Limits:
Adolescent
/
Female
/
Humans
Language:
En
Journal:
J Pediatr Adolesc Gynecol
Journal subject:
GINECOLOGIA
/
PEDIATRIA
Year:
2024
Document type:
Article
Country of publication: