Severe plexiform facial neurofibromatosis, type 1 with underdeveloped eyes and a novel NF1 mutation
A Thai woman, who was affected with neurofibromatosis type 1, was followed up and re-evaluated at ages 45, 61, and 67 years. Her mother and her three brothers were also affected. The proposita was very severely affected. She was born blind with underdeveloped eyeglobes and had large plexiform neurof...
محفوظ في:
المؤلفون الرئيسيون: | Piranit Nik Kantaputra, Ans van den Ouweland, Tumtip Sangruchi, Chanin Limwongse |
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التنسيق: | دورية |
منشور في: |
2018
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الموضوعات: | |
الوصول للمادة أونلاين: | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84862704574&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/51380 |
الوسوم: |
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المؤسسة: | Chiang Mai University |
مواد مشابهة
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Severe plexiform facial neurofibromatosis, type 1 with underdeveloped eyes and a novel NF1 mutation
بواسطة: Piranit Nik Kantaputra, وآخرون
منشور في: (2018) -
Severe plexiform facial neurofibromatosis, type 1 with underdeveloped eyes and a novel NF1 mutation
بواسطة: Kantaputra P.N., وآخرون
منشور في: (2014) -
Clinics in diagnostic imaging (96). Plexiform neurofibromatosis
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منشور في: (2014) -
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بواسطة: Courtney, Eliza, وآخرون
منشور في: (2022) -
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منشور في: (2018)