Prenatal diagnosis of 5p deletion syndrome: A case series report

Han ,  You Jung ,  Kwak 외 1명

Journal of genetic medicine

2017 .01

Prenatal diagnosis of 4p deletion syndrome: A case series report

Kwak ,  Dong Wook ,  Ahn 외 1명

Journal of genetic medicine

2017 .01

Effects of e2f3 gene deletion in mice

Ki-Hoan Nam ,  Hae-Rim Kim ,  Eun-Kyeung Kim 외 7명

한국실험동물학회 학술발표대회 논문집

2020 .02

Understanding of uterine cell type-specific function of microRNAs using Dgcr8 conditional knockout mice by multiple Cre systems

Yeon Sun Kim ,  Mi ,  a Pa 외 8명

한국실험동물학회 학술발표대회 논문집

2018 .01

A case of CHARGE syndrome featuring immunodeficiency and hypocalcemia

Son ,  Yu Yun ,  Lee 외 11명

Journal of genetic medicine

2015 .01

The First Korean Case of De Novo Proximal 4p Deletion Syndrome in a Child With Developmental Delay

Soyoung Pa ,  k ,  Byung Ryul Jeon 외 3명

Annals of Laboratory Medicine

2020 .01

Chromosome 11q13 deletion syndrome

Kim ,  Yu-Seon ,  Kim 외 7명

Clinical and Experimental Pediatrics

2016 .01

X-linked Hypophosphatemic Rickets, del(2)(q37.1;q37.3) Deletion Syndrome and Mosaic Turner Syndrome, mos 45,X/46,X, del(2)(q37.1;q37.3) in a 3-year-old Female

Alaina P. Vidma ,  B ,  ian Miyazaki 외 4명

대한골대사학회지

2017 .01

Overexpression of Tbx3 Predicts Poor Prognosis of Patients with Resectable Pancreatic Carcinoma

Wang ,  Hong-Cheng ,  Meng 외 7명

Asian Pacific journal of cancer prevention : APJCP

2015 .01

Non-Homologous End Joining Repair Mechanism-Mediated Deletion of CHD7 Gene in a Patient with Typical CHARGE Syndrome

이승준 ,  채종희 ,  이정애 외 5명

Annals of Laboratory Medicine

2015 .01

1p36 Deletion syndrome Presenting with Various Epileptic Semiologies

김애리 ,  이지원 ,  이문향 외 1명

대한소아신경학회지

2015 .12

A case of de novo 18p deletion syndrome with panhypopituitarism

A ,  am Yang ,  Jinsup Kim 외 4명

Annals of Pediatirc Endocrinology & Metabolism

2019 .01

Delayed Diagnosis of Chromosome 22q11.2 Deletion Syndrome Due to Late-Onset Generalized Epilepsy

이선경 ,  이응준 ,  권경현 외 2명

Journal of Clinical Neurology

2020 .01

A case of 18p chromosomal deletion encompassing GNAL in a patient with dystonia-parkinsonism

F ,  ancesco Cavallie ,  i

Journal Of Movement Disorders

2024 .04

Vascular compression syndromes: a pictorial review

Renato Fa ,  ina ,  Piet 외 15명

ULTRASONOGRAPHY

2022 .07

A Case of Partial Short Arm Deletion in Chromosome 9 with Inguinal Hernia, Testicular Cystic Lesion, and Arthrogryposis Multiplex Congenita

김은정 ,  정성훈 ,  박태성 외 1명

Neonatal medicine

2017 .01

Terminal Deletion of the Chromosome 4q with Hemivertebra: Case Report

Seung-Hyun Ko ,  Hyun Ju Lee ,  김창렬 외 2명

Perinatology

2020 .01

A Korean Case of De Novo 18q Deletion Syndrome With a Large Atrial Septal Defect and Cyanosis

김영진 ,  박태성 ,  한미영 외 2명

Annals of Laboratory Medicine

2015 .01

Diagnostic distal 16p11.2 deletion in a preterm infant with facial dysmorphism

Hyun ,  Ju Kyung ,  Jung 외 1명

Journal of genetic medicine

2018 .01

Two base pair deletion in IL2 receptor γ gene in NOD/SCID mice induces a highly severe immunodeficiency

Inseon Bak ,  Doo-Jin Kim ,  Hyoung-Chin Kim 외 4명

한국실험동물학회 학술발표대회 논문집

2020 .07