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아주대학교 의학문헌정보센터
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Pub Year
Title
AJOU Author(s)
2007
16q-linked autosomal dominant cerebellar ataxia in a Korean family.
김현주
,
이필휴
,
정선용
2018
3'-Sialyllactose as an inhibitor of p65 phosphorylation ameliorates the progression of experimental rheumatoid arthritis
강이중
,
양시영
,
정선용
2014
A biochemical and physicochemical comparison of two recombinant enzymes used for enzyme replacement therapies of hunter syndrome.
손영배
2013
A Case of CATCH22 Syndrome Diagnosed in Postmenopausal Woman
손영배
,
정윤석
2012
A Case of CATCH22 Syndrome with Normal Parathyroid Function
손영배
,
안소연
,
정윤석
2010
A case of donor-derived granulocytic sarcoma after allogeneic hematopoietic stem cell transplantation
강석윤
,
박준성
,
이현우
,
정선용
,
정성현
,
최진혁
,
한재호
2007
A Case of Down`s Syndrome with Thyrotoxic Crisis
김대중
,
김현주
,
김혜진
,
이관우
,
정윤석
2005
A Case of Familial Medullary Thyroid Carcinoma with a E768D Mutation in RET Proto-Oncogene
김대중
,
김연경
,
김철호
,
김현주
,
송경은
,
안상미
,
이관우
,
정선용
,
정선혜
,
정윤석
2007
A Case of Familial Multiple Endocrine Neoplasia Type 1 with MEN1 Gene Mutation.
김대중
,
김현주
,
김혜진
,
이관우
,
정선용
,
정윤석
,
최용준
2014
A Case of Neonatal Intrahepatic Cholestasis Caused by Citrin Deficiency (NICCD) Confirmed by SLC25A13 Mutation
손영배
,
장주영
2007
A Case of Resistance Syndrome to Thyroid Hormone Associated with Mutation (G345D) in the Thyroid Hormone Receptor Beta Gene
김대중
,
김현주
,
김혜진
,
이관우
,
정선용
,
정윤석
2001
A case of slipped capital femoral epiphysis developed during growth hormone treatment
김현만
,
김현주
,
이관우
,
이수진
,
정윤석
1998
A Case of Splenic Embolization Followed by Splenectomy with Preservation of Accessory Spleen in Gaucher’s Disease
김명욱
,
김현주
,
소의영
,
임현이
2017
A case report of pycnodysostosis with atypical femur fracture diagnosed by next-generation sequencing of candidate genes
손영배
,
송형근
,
정윤석
,
최용준
2022
A Comparison of the Antiosteoporotic Effects of Cornelian Cherry (Cornus mas L.) Extracts from Red and Yellow Fruits Containing Different Constituents of Polyphenols and Iridoids in Osteoblasts and Osteoclasts
박은국
,
정선용
2008
A Family Case of Complete Androgen Insensitivity Syndrome in Sisters due to a Novel Mutation in the Androgen Receptor Gene
김미란
,
김현주
,
정윤석
,
주희재
2014
A Korean case of neurofibromatosis type 1 with an exonic splicing enhancer site mutation
박상욱
,
손영배
,
정선용
2012
A Korean patient with Morquio B disease with a novel c.13_14insA mutation in the GLB1 gene
손영배
2009
A Novel COMP Gene Mutation in a Korean Kindred with Multiple Epiphyseal Dysplasia
고정민
,
곽규성
,
김현주
2010
A novel homozygous MMP2 mutation in a patient with Torg-Winchester syndrome.
김옥화
,
김현주
,
정선용
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아주대학교 의학문헌정보센터