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  *입력하신 저널에 한하여 검색결과를 보여줍니다. (예. Nature Genetics 또는 Nat. Genet. 로 정확히 입력)
한빛사논문    44건 정확도순날짜순
김도균 (Geisinger Health System, 현 University of Pennsylvania)
Human-Disease Phenotype Map Derived from PheWAS across 38,682 Individuals
Am. J. Hum. Genet., Volume 104, ISSUE 1, P55-64, January 03, 2019 | https://doi.org/10.1016/j.ajhg.2018.11.006
Genetics
정형록 (Baylor College of Medicine, Texas Children’s Hospital) 인터뷰
Bi-allelic Loss-of-Function Variants in DNMBP Cause Infantile Cataracts
Am. J. Hum. Genet., Volume 103, Issue 4, 4 October 2018, Pages 568-578 | https://doi.org/10.1016/j.ajhg.2018.09.004
Genetics, Genetics, Medicine
이종민 (Massachusetts General Hospital / Harvard Medical School, the..)
Genetic Modification of Huntington Disease Acts Early in the Prediagnosis Phase
Am. J. Hum. Genet., Available online 16 August 2018 | https://doi.org/10.1016/j.ajhg.2018.07.017
Genetics
이상홍 (University of South Australia, University of New England, Un..)
Estimation of Genetic Correlation via Linkage Disequilibrium Score Regression and Genomic Restricted Maximum Likelihood
Am. J. Hum. Genet., Volume 102, Issue 6, 7 June 2018, Pages 1185-1194 | https://doi.org/10.1016/j.ajhg.2018.03.021
Genetics
손정훈 (Columbia University)
Deep Phenotyping on Electronic Health Records Facilitates Genetic Diagnosis by Clinical Exomes
Am. J. Hum. Genet., Published: June 28, 2018 | DOI: https://doi.org/10.1016/j.ajhg.2018.05.010
Genetics
윤완희 (Baylor College of Medicine) 인터뷰
Biallelic Mutations in ATP5F1D, which Encodes a Subunit of ATP Synthase, Cause a Metabolic Disorder
Am. J. Hum. Genet., Volume 102, Issue 3, 1 March 2018, Pages 494-504 | https://doi.org/10.1016/j.ajhg.2018.01.020
Genetics
이승근 (University of Michigan)
A Fast and Accurate Algorithm to Test for Binary Phenotypes and Its Application to PheWAS
Am. J. Hum. Genet., Volume 101, Issue 1, 6 July 2017, Pages 37-49 | https://doi.org/10.1016/j.ajhg.2017.05.014
Genetics
김선영 (Texas Children’s Hospital, Baylor College of Medicine)
MARRVEL: Integration of Human and Model Organism Genetic Resources to Facilitate Functional Annotation of the Human Genome
Am. J. Hum. Genet., Available online 11 May 2017, https://doi.org/10.1016/j.ajhg.2017.04.010
Genetics
윤완희 (Baylor College of Medicine)
Recurrent De Novo and Biallelic Variation of ATAD3A, Encoding a Mitochondrial Membrane Protein, Results in Distinct Neurological Syndromes
Am. J. Hum. Genet., Available online 15 September 2016 | http://dx.doi.org/10.1016/j.ajhg.2016.08.007
Genetics
설재훈 (Brigham and Women’s Hospital and Harvard Medical School, Uni..)
Increasing Generality and Power of Rare-Variant Tests by Utilizing Extended Pedigrees
Am. J. Hum. Genet., Available online 22 September 2016 | http://dx.doi.org/10.1016/j.ajhg.2016.08.015
Genetics
(주)비아이코퍼레이션
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나노스캐닝현미경(SCANNING PROBE MICROSCOPE, NANOMAN-0...
모델명 없음 | 한국표준과학연구원 | 2003.08.06
현미경시스템(Variable Temperature UHV Scanning Prob...
모델명 없음 | 한국표준과학연구원 | 2003.04.02
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molecular_biology 1
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