1p36 deletion syndrome: Review and mapping with further characterization of the phenotype, a new cohort of 86 patients.
Am J Med Genet A
; 191(2): 445-458, 2023 02.
Article
in En
| MEDLINE
| ID: mdl-36369750
Key words
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Down Syndrome
/
DiGeorge Syndrome
/
Epilepsy
/
Intellectual Disability
/
Microcephaly
Type of study:
Risk_factors_studies
Limits:
Humans
Language:
En
Journal:
Am J Med Genet A
Journal subject:
GENETICA MEDICA
Year:
2023
Document type:
Article
Affiliation country:
Country of publication: