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Entire PTCH1 deletion is a common event in point mutation-negative cases with nevoid basal cell carcinoma syndrome in Japan |
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| Authors: | Nagao K Fujii K Saito K Sugita K Endo M Motojima T Hatsuse H Miyashita T |
| Affiliation: | 1. Department of Molecular Genetics, Kitasato University School of Medicine, Sagamihara, Japan;2. Department of Pediatrics, Chiba University Graduate School of Medicine, Chiba, Japan;3. Institute of Medical Genetics, Tokyo Women's Medical University, Tokyo, Japan;4. Division of Child Health, Faculty of Education, Chiba University, Chiba, Japan;5. Department of Pediatrics, Motojima General Hospital, Ota, Japan |
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| 本文献已被 PubMed 等数据库收录！ | |