Diagnostic and clinical utility of next-generation sequencing in children born with multiple congenital anomalies in the China neonatal genomes project.
Hum Mutat
; 42(4): 434-444, 2021 04.
Article
in En
| MEDLINE
| ID: mdl-33502061
Key words
Full text:
1
Database:
MEDLINE
Main subject:
DNA Copy Number Variations
/
High-Throughput Nucleotide Sequencing
Type of study:
Diagnostic_studies
/
Etiology_studies
/
Incidence_studies
/
Observational_studies
/
Risk_factors_studies
Limits:
Humans
/
Newborn
Country/Region as subject:
Asia
Language:
En
Journal:
Hum Mutat
Journal subject:
GENETICA MEDICA
Year:
2021
Type:
Article
Affiliation country:
China