A case of de novo 18p deletion syndrome with panhypopituitarism.

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第一作者： Aram,Yang

第一单位： Department of Pediatrics, Inha University Hospital, Inha University College of Medicine, Incheon, Korea.

作者： Aram,Yang ^[1] ; Jinsup,Kim ^[2] ; Sung Yoon,Cho ^[3] ; Ji-Eun,Lee ^[1] ; Hee-Jin,Kim ^[4] ; Dong-Kyu,Jin ^[3]

作者单位： Department of Pediatrics, Inha University Hospital, Inha University College of Medicine, Incheon, Korea. ^[1] Department of Pediatrics, Hanyang University Medical Center, Hanyang University School of Medicine, Seoul, Korea. ^[2] Department of Pediatrics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea. ^[3] Department of Laboratory Medicine & Genetics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea. ^[4]

关键词 Growth hormone SNP microarray 18p deletion syndrome

DOI 10.6065/apem.2019.24.1.60

PMID 30943682

发布时间 2020-09-30

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Annals of pediatric endocrinology & metabolism

2019年24卷1期

60-63页

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A case of de novo 18p deletion syndrome with panhypopituitarism.

Annals of pediatric endocrinology & metabolism

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Annals of pediatric endocrinology & metabolism

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A case of de novo 18p deletion syndrome with panhypopituitarism.

Annals of pediatric endocrinology & metabolism

相似文献

Annals of pediatric endocrinology & metabolism

相关期刊

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