Co-occurrence of Sturge–Weber syndrome and Klippel–Trenaunay–Weber syndrome phenotype: Consideration of the historical aspect

Yuri Sakaguchi; Toshiki Takenouchi; Tomoko Uehara; Kazuo Kishi; Takao Takahashi; Kenjiro Kosaki

doi:10.1002/ajmg.a.38363

Co-occurrence of Sturge–Weber syndrome and Klippel–Trenaunay–Weber syndrome phenotype: Consideration of the historical aspect

Yuri Sakaguchi, Toshiki Takenouchi, Tomoko Uehara, Kazuo Kishi, Takao Takahashi, Kenjiro Kosaki

研究成果: Letter › 査読

本文言語	English
ページ（範囲）	2831-2833
ページ数	3
ジャーナル	American Journal of Medical Genetics, Part A
巻	173
号	10
DOI	https://doi.org/10.1002/ajmg.a.38363
出版ステータス	Published - 2017 10月

ASJC Scopus subject areas

遺伝学
遺伝学（臨床）

文献へのアクセス

10.1002/ajmg.a.38363

他のファイルとリンク

引用スタイル

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title = "Co-occurrence of Sturge–Weber syndrome and Klippel–Trenaunay–Weber syndrome phenotype: Consideration of the historical aspect",

author = "Yuri Sakaguchi and Toshiki Takenouchi and Tomoko Uehara and Kazuo Kishi and Takao Takahashi and Kenjiro Kosaki",

note = "Funding Information: Japan Agency for Medical Research and Development Initiative on Rare and Undiagnosed Diseases, Grant number: Labor, and Welfare Research on Rare and Intractable Diseases Funding Information: We thank Mrs. Yumi Obayashi and Keiko Tsukue for their technical assistance in the preparation of this article. This work was supported by Research on Rare and Intractable Diseases from the Ministry of Health, Labor, and Welfare, Japan, and Initiative on Rare and Undiagnosed Diseases (Grant number: 16ek0109166h0002) from the Japan Agency for Medical Research and Development.",

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AU - Uehara, Tomoko

AU - Kishi, Kazuo

AU - Takahashi, Takao

AU - Kosaki, Kenjiro

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