Hypotonic infant with Pallister–Killian syndrome diagnosed by cytogenetic microarray, without pigmentary skin changes and malformations
J Genet
; 2020 Apr; 99: 1-3
Article
| IMSEAR
| ID: sea-215531
Texte intégral:
1
Indice:
IMSEAR
Type d'étude:
Diagnostic_studies
Texte intégral:
J Genet
Année:
2020
Type:
Article