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아주대학교 의학문헌정보센터
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고, 정민
Not currently indexed
[School of Medicine / Graduate School of Medicine] - [Medical Genetics]
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-
ISNI
0000000467813989
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-
SCOPUS
-
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(15)
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(0)
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(0)
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(0)
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Showing results 1 to 15 of 15
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Pub Year
Title
AJOU Author(s)
2011
Genetic Variations of GNRH1, GNRHR and GPR54 Genes in Korean Girls with Central Precocious Puberty
고정민
,
이해상
,
황진순
2010
The natural history and prognostic factors of Graves’ disease in Korean children and adolescents
고정민
2010
Early Diagnosis of Fabry Disease in a Patient with Toe Tip Pain
고정민
,
김찬
,
한경림
2010
Phenotypic and Cytogenetic Delineation of Six Korean Children with Kabuki Syndrome
고정민
,
김현주
2010
Partial tetrasomy of chromosome 22q11.1 resulting from a supernumerary isodicentric marker chromosome in a boy with cat-eye syndrome.
고정민
,
배기수
2010
Influence of parental origin of the X chromosome on physical phenotypes and GH responsiveness of patients with Turner syndrome.
고정민
2010
Novel mutation in SLC6A19 causing late-onset seizures in Hartnup disorder.
고정민
2010
The common exon 3 polymorphism of the growth hormone receptor gene and the effect of growth hormone therapy on growth in Korean patients with Turner syndrome.
고정민
2010
Clinical characterization and analysis of the SRD5A2 gene in six Korean patients with 5alpha-reductase type 2 deficiency.
고정민
2010
Clinical features and outcomes of holoprosencephaly in Korea.
고정민
,
김성환
2010
KISS1 gene analysis in Korean girls with central precocious puberty: a polymorphism, p.P110T, suggested to exert a protective effect.
고정민
,
황진순
2009
A Novel COMP Gene Mutation in a Korean Kindred with Multiple Epiphyseal Dysplasia
고정민
,
곽규성
,
김현주
2009
The Clinical Features, Immunostaining and Genetic Study in Duchenne/Becker Muscular Dystrophy
고정민
2009
Novel Therapies for Type 2 Diabetes Mellitus
고정민
2009
A case of Antley-Bixler syndrome caused by compound heterozygous mutations of the cytochrome P450 oxidoreductase gene.
고정민
1
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아주대학교 의학문헌정보센터