Detecting X‐linked common and rare variant effects in family‐based sequencing studies.
Autor: | Turkmen, Asuman S., Lin, Shili |
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Zdroj: | Genetic Epidemiology; Feb2021, Vol. 45 Issue 1, p36-45, 10p |
Databáze: | Complementary Index |
Externí odkaz: |
Autor: | Turkmen, Asuman S., Lin, Shili |
---|---|
Zdroj: | Genetic Epidemiology; Feb2021, Vol. 45 Issue 1, p36-45, 10p |
Databáze: | Complementary Index |
Externí odkaz: |