Expanding the spectrum of syndromic PPP2R3C-related XY gonadal dysgenesis to XX gonadal dysgenesis.
Clin Genet
; 101(2): 221-232, 2022 02.
Article
in En
| MEDLINE
| ID: mdl-34750818
Key words
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Phenotype
/
Gonadal Dysgenesis, 46,XX
/
Protein Phosphatase 2
/
Gonadal Dysgenesis, 46,XY
/
Mutation
Type of study:
Diagnostic_studies
/
Prognostic_studies
Limits:
Female
/
Humans
/
Male
Language:
En
Journal:
Clin Genet
Year:
2022
Document type:
Article
Affiliation country:
Country of publication: