A case report and mechanism analysis of a normal phenotype mosaic 47, XXY complicated by paternal iUPD (9) who had a normal PGD result.
BMC Med Genet
; 20(1): 172, 2019 11 07.
Article
in En
| MEDLINE
| ID: mdl-31699048
Key words
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Phenotype
/
Sex Chromosome Aberrations
/
Preimplantation Diagnosis
/
Uniparental Disomy
Type of study:
Diagnostic_studies
Limits:
Adult
/
Female
/
Humans
/
Male
/
Newborn
/
Pregnancy
Language:
En
Journal:
BMC Med Genet
Journal subject:
GENETICA MEDICA
Year:
2019
Document type:
Article
Country of publication:
Reino Unido