Severe manifestations of hand-foot-genital syndrome associated with a novelHOXA13mutation

Author:

Imagawa Eri1,Kayserili Hülya2,Nishimura Gen3,Nakashima Mitsuko1,Tsurusaki Yoshinori1,Saitsu Hirotomo1,Ikegawa Shiro4,Matsumoto Naomichi1,Miyake Noriko1

Affiliation:

1. Department of Human Genetics; Yokohama City University Graduate School of Medicine; Yokohama Japan

2. Medical Genetics Department, Istanbul Medical Faculty; Istanbul University; Fatih, Istanbul Turkey

3. Department of Pediatric Imaging; Tokyo Metropolitan Children's Medical Center; Fuchu Japan

4. Laboratory of Bone and Joint Diseases; Center for Genomic Medicine, RIKEN; Tokyo Japan

Funder

Ministry of Health, Labour, and Welfare of Japan

Ministry of Education, Culture, Sports, Science and Technology

Strategic Research Program for Brain Sciences

Ministry of Education, Culture, Sports, Science, and Technology of Japan

Japan Society for the Promotion of Science

Takeda Science Foundation

Yokohama Foundation for the Advancement of Medical Science

Hayashi Memorial Foundation for Female Natural Scientists

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Cited by 14 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Hand-foot-genital syndrome due to a duplication variant in the GC-rich region of HOXA13;European Journal of Medical Genetics;2023-03

2. Genetic and phenotypic continuum of HOXA genes: A case with double HOXA9/HOXA13 mutations;Molecular Medicine Reports;2023-01-27

3. An unusual manifestation of Hand-Foot-Genital Syndrome: Embryonal Rhabdomyosarcoma - A case report;Annals of Medicine and Surgery;2021-02

4. Hereditary and Congenital Nail Disorders;Baran & Dawber's Diseases of the Nails and their Management;2018-12-07

5. Developmental biology of the upper limb;Hand Surgery and Rehabilitation;2018-10

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