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아주대학교 의학문헌정보센터
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Showing results 1 to 3 of 3
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2019
Deletion of exons 16-17b of CFTR is frequently identified in Korean patients with cystic fibrosis
손영배
,
장주영
1995
Heterozygosity for an exon 12 splicing mutation and a W234G missense mutation in an American child with chronic tyrosinemia type 1.
한시훈
2010
KISS1 gene analysis in Korean girls with central precocious puberty: a polymorphism, p.P110T, suggested to exert a protective effect.
고정민
,
황진순
1
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아주대학교 의학문헌정보센터
