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Volume 155, Issue 6 , Pages 900-903.e1 , December 2009

Maternal Uniparental Disomy 14 Syndrome Demonstrates Prader-Willi Syndrome-Like Phenotype

Kana Hosoki, MS
- Department of Pediatrics, Hokkaido University Graduate School of Medicine, Sapporo, Japan
Masayo Kagami, MD, PhD
- Department of Endocrinology and Metabolism, National Research Institute for Child Health and Development, Tokyo, Japan
Touju Tanaka, MD, PhD
- Division of Clinical Genetics and Molecular Medicine, National Research Institute for Child Health and Development, Tokyo, Japan
Masaya Kubota, MD, PhD
- Department of Pediatric Neurology, National Research Institute for Child Health and Development, Tokyo, Japan
Kenji Kurosawa, MD, PhD
- Division of Medical Genetics, Kanagawa Children's Medical Center, Yokohama, Japan
Mitsuhiro Kato, MD, PhD
- Department of Pediatrics, Yamagata University School of Medicine, Yamagata, Japan
Kimiaki Uetake, MD
- Department of Pediatrics, Obihiro Kosei Hospital, Obihiro, Japan
Jun Tohyama, MD, PhD
- Department of Pediatrics, Nishi-Niigata Chuo National Hospital, Niigata, Japan
Tsutomu Ogata, MD, PhD
- Department of Endocrinology and Metabolism, National Research Institute for Child Health and Development, Tokyo, Japan
Shinji Saitoh, MD, PhD
- Department of Pediatrics, Hokkaido University Graduate School of Medicine, Sapporo, Japan
- Reprint requests: Shinji Saitoh, MD, PhD, Department of Pediatrics, Hokkaido University, Graduate School of Medicine, North 15, West 7, Kita-ku, Sapporo, 060-8638, Japan.

Received 20 March 2009 ,Revised 6 May 2009 ,Accepted 22 June 2009.

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This work was partially supported by a grant from the Ministry of Education, Science and Culture of Japan. The authors declare no conflicts of interest.

PII: S0022-3476(09)00614-3

doi: 10.1016/j.jpeds.2009.06.045

« Previous Next » The Journal of Pediatrics
Volume 155, Issue 6 , Pages 900-903.e1 , December 2009