Identification of a novel variant of SCARF2 in a Jordanian family with a van den Ende-Gupta Syndrome and literature review.
Clin Dysmorphol
; 31(3): 157-161, 2022 07 01.
Article
in En
| MEDLINE
| ID: mdl-35256560
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Abnormalities, Multiple
/
Blepharophimosis
/
Arachnodactyly
Type of study:
Diagnostic_studies
Limits:
Humans
Country/Region as subject:
Asia
Language:
En
Journal:
Clin Dysmorphol
Journal subject:
TERATOLOGIA
Year:
2022
Document type:
Article