X-linked VACTERL-H caused by deletion of exon 3 in FANCB: A case report.
Congenit Anom (Kyoto)
; 58(5): 171-172, 2018 Sep.
Article
in En
| MEDLINE
| ID: mdl-29232005
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Base Sequence
/
Sequence Deletion
/
Cardiovascular Abnormalities
/
Genetic Diseases, X-Linked
/
Digestive System Abnormalities
/
Fanconi Anemia Complementation Group Proteins
/
Hydrocephalus
/
Musculoskeletal Abnormalities
Type of study:
Diagnostic_studies
Limits:
Female
/
Humans
/
Infant
/
Male
/
Newborn
/
Pregnancy
Language:
En
Journal:
Congenit Anom (Kyoto)
Journal subject:
TERATOLOGIA
Year:
2018
Document type:
Article
Affiliation country:
Country of publication: