Application of Chromosome Microarray Analysis in the Investigation of Developmental Disabilities and Congenital Anomalies: Single Center Experience and Review of NRXN3 and NEDD4L Deletions.
Mol Syndromol
; 11(4): 197-206, 2020 Nov.
Article
en En
| MEDLINE
| ID: mdl-33224013
Texto completo:
1
Bases de datos:
MEDLINE
Tipo de estudio:
Observational_studies
/
Risk_factors_studies
Idioma:
En
Revista:
Mol Syndromol
Año:
2020
Tipo del documento:
Article
País de afiliación:
Turquía