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아주대학교 의학문헌정보센터
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Showing results 1 to 7 of 7
Pub Year
Title
Author(s)
2007
16q-linked autosomal dominant cerebellar ataxia in a Korean family.
김현주
,
이필휴
,
정선용
2004
A novel point mutation in PMP22 gene associated with a familial case of Charcot-Marie-Tooth disease type 1A with sensorineural deafness.
주인수
,
허균
2006
A rare extracellular D631Y germline mutation of the RET proto-oncogene in two Korean families with multiple endocrine neoplasia 2A.
김대중
2013
Dietary intake and breast cancer among carriers and noncarriers of BRCA mutations in the Korean Hereditary Breast Cancer Study.
정용식
2013
Mutation spectrum of NF1 and clinical characteristics in 78 Korean patients with neurofibromatosis type 1.
김현주
,
손영배
,
정선용
2006
Relationship between metabolic syndrome and familial history of hypertension/stroke, diabetes, and cardiovascular disease.
이관우
,
전기홍
2000
The first successful prenatal diagnosis on a Korean family with citrullinemia.
한시훈
1
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아주대학교 의학문헌정보센터
