Increased runs of homozygosity in the autosomal genome of Brazilian individuals with neurodevelopmental delay/intellectual disability and/or multiple congenital anomalies investigated by chromosomal microarray analysis.
第一单位:
Universidade de Campinas, Faculdade de Ciências Médicas, Departamento de Medicina Translacional, Campinas, SP, Brazil.
作者:
DOI
10.1590/1678-4685-GMB-2020-0480
PMID
35238326
发布时间
2022-07-16
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Genetics and molecular biology
e20200480页
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