A novelWTXmutation in a female patient with osteopathia striata with cranial sclerosis and hepatoblastoma-Reference-Cited by-同舟云学术

A novelWTXmutation in a female patient with osteopathia striata with cranial sclerosis and hepatoblastoma

Published:2014-01-23 Issue:4 Volume:164 Page:998-1002
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Fujita Atsushi¹,Ochi Nobuhiko²,Fujimaki Hidehiko³,Muramatsu Hideki⁴,Takahashi Yoshiyuki⁴,Natsume Jun⁴,Kojima Seiji⁴,Nakashima Mitsuko¹,Tsurusaki Yoshinori¹,Saitsu Hirotomo¹,Matsumoto Naomichi¹,Miyake Noriko¹

Affiliation:

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

2. Department of Pediatrics; Aichi Prefectural Rehabilitation Center for Children with Disabilities Daini Aoitori Gakuen; Okazaki Japan

3. Division of Neonatology, Center for Maternal-Neonatal Care; Nagoya University Hospital; Nagoya Japan

4. Department of Pediatrics; Nagoya University Graduate School of Medicine; Nagoya Japan

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.36369/fullpdf

Reference25 articles.

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2. Osteopathia striata with cranial sclerosis: Literature reappraisal argues for X-linked inheritance;Behninger;Genet Couns,2000

3. Conductive hearing loss in osteopathia striata-cranial sclerosis;Berenholz;Otolaryngol Head Neck Surg,2002

4. Wnt/beta-catenin signaling and disease;Clevers;Cell,2012

5. Risk of cancer during the first four years of life in children from the Beckwith-Wiedemann syndrome registry;DeBaun;J Pediatr,1998

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