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

Research output: Contribution to journal › Letter › peer-review

Original language	English
Pages (from-to)	2831-2833
Number of pages	3
Journal	American Journal of Medical Genetics, Part A
Volume	173
Issue number	10
DOIs	https://doi.org/10.1002/ajmg.a.38363
Publication status	Published - 2017 Oct

ASJC Scopus subject areas

Genetics
Genetics(clinical)

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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.",

year = "2017",

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T1 - Co-occurrence of Sturge–Weber syndrome and Klippel–Trenaunay–Weber syndrome phenotype

T2 - Consideration of the historical aspect

AU - Sakaguchi, Yuri

AU - Takenouchi, Toshiki

AU - Uehara, Tomoko

AU - Kishi, Kazuo

AU - Takahashi, Takao

AU - Kosaki, Kenjiro

N1 - 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.

PY - 2017/10

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SN - 1552-4825

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ER -

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

ASJC Scopus subject areas

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