지원사업
학술연구/단체지원/교육 등 연구자 활동을 지속하도록 DBpia가 지원하고 있어요.
커뮤니티
연구자들이 자신의 연구와 전문성을 널리 알리고, 새로운 협력의 기회를 만들 수 있는 네트워킹 공간이에요.
이용수
등록된 정보가 없습니다.
논문 유사도에 따라 DBpia 가 추천하는 논문입니다. 함께 보면 좋을 연관 논문을 확인해보세요!
An analysis of Y-chromosome microdeletion in infertile Korean men with severe oligozoospermia or azoospermia
Investigative and Clinical Urology
2024 .01
A Case of Partial Short Arm Deletion in Chromosome 9 with Inguinal Hernia, Testicular Cystic Lesion, and Arthrogryposis Multiplex Congenita
Neonatal medicine
2017 .01
Genetic Screening for Chromosomal Abnormalities and Y Chromosome Microdeletions in 846 Infertile Korean Men
Laboratory Medicine Online
2018 .01
Terminal Deletion of the Chromosome 4q with Hemivertebra: Case Report
Perinatology
2020 .01
Deletion of 20p13 and Duplication of 20p13p12.3 in a Patient with Delayed Speech and Development
Annals of Laboratory Medicine
2018 .01
A boy with 46,X,+mar presenting gynecomastia and short stature
Annals of Pediatirc Endocrinology & Metabolism
2017 .01
Role of CFP1 in spermatogenesis
한국실험동물학회 학술발표대회 논문집
2016 .08
A Patient With Delayed Development Resulting From De Novo Duplication of 7q36.1-q36.3 and Deletion of 9p24.3
Annals of Rehabilitation Medicine
2017 .01
Chromosome 11q13 deletion syndrome
Clinical and Experimental Pediatrics
2016 .01
Successful onco-testicular sperm extraction from a testicular cancer patient with a single testis and azoospermia
Clinical and experimental reproductive medicine : CERM
2018 .01
14q12q13.3 Deletion Diagnosed Using Chromosomal Microarray Analysis in an Infant Showing Seizures, Hypoplasia of the Corpus Callosum, and Developmental Delay
Neonatal medicine
2020 .01
Congenital Absence of the Bilateral Internal Carotid Arteries: a Case Report
Investigative Magnetic Resonance Imaging
2021 .09
De novo interstitial deletion of 15q22q23 with global developmental delay and hypotonia: the first Korean case
Clinical and Experimental Pediatrics
2015 .01
Dynamic regulation of TLE3 expression during spermatogenesis in mouse testis
한국실험동물학회 학술발표대회 논문집
2017 .08
Prenatal diagnosis of 4p deletion syndrome: A case series report
Journal of genetic medicine
2017 .01
Delayed Diagnosis of Chromosome 22q11.2 Deletion Syndrome Due to Late-Onset Generalized Epilepsy
Journal of Clinical Neurology
2020 .01
Diagnostic distal 16p11.2 deletion in a preterm infant with facial dysmorphism
Journal of genetic medicine
2018 .01
Anesthetic management of a patient with chromosome 6p duplication: a case report
Journal of dental anesthesia and pain medicine
2017 .01
Birth seasonality in Korean Prader-Willi syndrome with chromosome 15 microdeletion
Annals of Pediatirc Endocrinology & Metabolism
2015 .01
MEF2C-Related 5q14.3 Microdeletion Syndrome Detected by Array CGH: A Case Report
Annals of Rehabilitation Medicine
2015 .01
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