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아주대학교 의학문헌정보센터
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Browsing by Keyword : Genetic Association Studies
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Showing results 27 to 40 of 40
Pub Year
Title
AJOU Author(s)
2010
Linkage and association studies of joint morbidity from rheumatoid arthritis.
민경복
2022
Mutation spectrum and genotype–phenotype correlations in 157 Korean CADASIL patients: a multicenter study
박서진
2013
Mutation spectrum of NF1 and clinical characteristics in 78 Korean patients with neurofibromatosis type 1.
김현주
,
손영배
,
정선용
2017
No association between estrogen receptor gene polymorphisms and premature thelarche in girls
윤종서
,
이해상
,
황진순
2018
Nonsynonymous Variants in PAX4 and GLP1R Are Associated With Type 2 Diabetes in an East Asian Population
조남한
2014
Overgrowth syndrome associated with a gain-of-function mutation of the natriuretic peptide receptor 2 (NPR2) gene.
김옥화
2012
Prioritization of SNPs for genome-wide association studies using an interaction model of genetic variation, gene expression, and trait variation
백효정
2012
Response to growth hormone therapy in children with Noonan syndrome: correlation with or without PTPN11 gene mutation
황진순
2011
Revisit of multiple epiphyseal dysplasia: ethnic difference in genotypes and comparison of radiographic features linked to the COMP and MATN3 genes.
김옥화
2014
Single nucleotide polymorphisms associated with abnormal coronary microvascular function.
최병주
2010
The genetic association of the FPRL1 promoter polymorphism with chronic urticaria in a Korean population.
김승현
,
박해심
2012
TRPV4-pathy manifesting both skeletal dysplasia and peripheral neuropathy: a report of three patients
김옥화
2011
Whole-exome sequencing detects somatic mutations of IDH1 in metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria (MC-HGA).
김옥화
2011
Whole-exome sequencing identifies mutations of KIF22 in spondyloepimetaphyseal dysplasia with joint laxity, leptodactylic type.
김옥화
1
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아주대학교 의학문헌정보센터