首页> Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology> Combined pituitary hormone deficiency with unique pituitary dysplasia and morning glory syndrome related to a heterozygous PROKR2 mutation.

Combined pituitary hormone deficiency with unique pituitary dysplasia and morning glory syndrome related to a heterozygous PROKR2 mutation.

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第一作者： Yumi,Asakura

第一单位： Department of Endocrinology and Metabolism, Kanagawa Children's Medical Center, Yokohama, Japan.

作者： Yumi,Asakura ^[1] ; Koji,Muroya ^[1] ; Junko,Hanakawa ^[1] ; Takeshi,Sato ^[2] ; Noriko,Aida ^[3] ; Satoshi,Narumi ^[4] ; Tomonobu,Hasegawa ^[4] ; Masanori,Adachi ^[1]

作者单位： Department of Endocrinology and Metabolism, Kanagawa Children's Medical Center, Yokohama, Japan. ^[1] Department of Endocrinology and Metabolism, Kanagawa Children's Medical Center, Yokohama, Japan ; Department of Pediatrics, Keio University School of Medicine, Tokyo, Japan. ^[2] Department of Radiology, Kanagawa Children's Medical Center, Yokohama, Japan. ^[3] Department of Pediatrics, Keio University School of Medicine, Tokyo, Japan. ^[4]

关键词 PROK2 PROKR2 combined pituitary hormone deficiency (CPHD)morning glory syndrome pituitary dysplasia

DOI 10.1297/cpe.24.27

PMID 25678757

发布时间 2020-09-30

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Clinical pediatric endocrinology

2015年24卷1期

27-32页

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Clinical pediatric endocrinology

2015年24卷1期

27-32页

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Combined pituitary hormone deficiency with unique pituitary dysplasia and morning glory syndrome related to a heterozygous PROKR2 mutation.

Clinical pediatric endocrinology

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Clinical pediatric endocrinology

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Combined pituitary hormone deficiency with unique pituitary dysplasia and morning glory syndrome related to a heterozygous PROKR2 mutation.

Clinical pediatric endocrinology

相似文献

同项目论文

Clinical pediatric endocrinology

相关期刊

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