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MeSH:(22q11 Deletion Syndrome*)

1.Monosomy 22 Mosaicism Associated Thrombocytopenia Presenting as Behcet's Disease

Ji Yoon KIM ; Ki Hyeong LEE ; Sang Cheol LEE ; Ji Yeoun LEE

Clinical Pediatric Hematology-Oncology 2012;19(1):40-43

2.Analysis of genome copy number variations in fetuses with isolated ventricular septal defect and a literature review.

Panlai SHI ; Yaqin HOU ; Duo CHEN ; Yanjie XIA ; Xiaofan ZHU ; Gege SUN ; Qianqian LI ; Mingcong SHE ; Xiangdong KONG

Chinese Journal of Medical Genetics 2023;40(3):317-321

3.Genetic Syndromes associated with Congenital Heart Disease.

Jung Min KO

Korean Circulation Journal 2015;45(5):357-361

4.Prenatal ultrasonic characteristics and genetic analysis of fetuses with chromosome 22q11 microdeletion syndrome.

Meiying CAI ; Na LIN ; Linjuan SU ; Xiaoqing WU ; Xiaorui XIE ; Ying LI ; Hailong HUANG ; Liangpu XU

Chinese Journal of Medical Genetics 2021;38(9):853-856

5.A Case Report of Schizophrenia Patient with 22q11 Deletion Syndrome.

Soo Young BHANG ; Chang Yoon KIM ; Yeon Ho JOO ; Eul Ju SEU ; Han Euk RYU

Journal of Korean Neuropsychiatric Association 2003;42(4):528-531

6.Delayed diagnosis of 22q11 deletion syndrome due to late onset hypocalcemia in a 11-year-old girl with imperforated anus.

Dong Yoon YOO ; Hae Jung KIM ; Kee Hyun CHO ; Eun Byul KWON ; Eun Gyong YOO

Annals of Pediatric Endocrinology & Metabolism 2017;22(2):133-138

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