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논문 유사도에 따라 DBpia 가 추천하는 논문입니다. 함께 보면 좋을 연관 논문을 확인해보세요!
A Case of Single-step Mutations at Two Short Tandem Repeat loci (D13S317 and DXS10148) among Three Generations of a Korean Family
대한의생명과학회지
2022 .12
Improvement of the Discrimination Capacity through the Expansion of Y Chromosomal STR Markers
대한의생명과학회지
2023 .12
A Review of Extended STR Loci and DNA Database
대한의생명과학회지
2022 .09
STR 검사에서 관찰된 모자이시즘 사례
대한법의학회지
2021 .11
Sequence Variations of 31 Y-Chromosomal Short Tandem Repeats Analyzed by Massively Parallel Sequencing in Three U.S. Population Groups and Korean Population
Journal of Korean Medical Science
2022 .02
Novel Germline Mutations of BRCA1 and BRCA2 in Korean Familial Breast Cancer Patients
전남의대학술지
2019 .01
Looking Back at Our 5-Year Experience of Paternity Testing: A Summary
대한법의학회지
2016 .01
The Association of Acquired T790M Mutation with Clinical Characteristics after Resistance to First-Line Epidermal Growth Factor Receptor Tyrosine Kinase Inhibitor in Lung Adenocarcinoma
Cancer Research and Treatment
2018 .01
Prevalence of PALB2 Germline Mutations in Early-onset and Familial Breast/Ovarian Cancer Patients from Pakistan
Cancer Research and Treatment
2019 .01
Novel SLC37A4 Mutations in Korean Patients With Glycogen Storage Disease Ib
Annals of Laboratory Medicine
2017 .01
Congenital hypothyroidism due to thyroglobulin deficiency: a case report with a novel mutation in TG gene
Annals of Pediatirc Endocrinology & Metabolism
2019 .01
Effectivity of several DNA polymerases for str analysis of contaminated DNAs
대한체질인류학회 학술대회 연제 초록
2016 .05
Mutation Analysis of IDH1/2 Genes in Unselected De novo Acute Myeloid Leukaemia Patients in India - Identification of A Novel IDH2 Mutation
Asian Pacific journal of cancer prevention : APJCP
2015 .01
Incidence, Clinical Features, and Prognostic Impact of CALR Exon 9 Mutations in Essential Thrombocythemia and Primary Myelofibrosis: An Experience of a Single Tertiary Hospital in Korea
Annals of Laboratory Medicine
2015 .01
Mutations in GJB2 as Major Causes of Autosomal Recessive Non-Syndromic Hearing Loss: First Report of c.299-300delAT Mutation in Kurdish Population of Iran
Journal of Audiology & Otology
2019 .01
Types of 23S Ribosomal RNA Point Mutations and Therapeutic Outcomes for Helicobacter pylori
Gut and Liver
2021 .01
Genetic diagnosis of autosomal dominant polycystic kidney disease: linkage analysis versus direct mutation analysis
Kidney Research and Clinical Practice
2016 .01
Validation of Reduced-volume Reaction in the PowerQuant® System for human DNA Quantification
대한의생명과학회지
2020 .12
Efficacy of Stiripentol in Dravet Syndrome with or without SCN1A Mutations
Journal of Clinical Neurology
2018 .01
Genetic Profiles of Korean Patients With Glucose-6-Phosphate Dehydrogenase Deficiency
Annals of Laboratory Medicine
2017 .01
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