Nevoid basal carcinoma syndrome (Gorlin syndrome) and pronounced androgenic alopecia in a woman with a novel mutation p.Leu1159fsx32 in the PTCH gene
スポンサーリンク
概要
- 論文の詳細を見る
- 2011-12-01
著者
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Willems Patrick
Gendia Network
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Kanavakis Emmanuel
Department Of Medical Genetics Medical School University Of Athens
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KANAVAKIS Emmanuel
Department of Medical Genetics, University of Athens, "Aghia Sophia" Children's Hospital
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KITSIOU-TZELI Sofia
Department of Medical Genetics, University of Athens, "Aghia Sophia" Children's Hospital
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KOSMADAKI Maria
Department of Dermatology, University of Athens, "Andreas Syggros" Hospital
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LEZE Eleni
Department of Medical Genetics, University of Athens, "Aghia Sophia" Children's Hospital
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VRETTOU Christine
Department of Medical Genetics, University of Athens, "Aghia Sophia" Children's Hospital
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KATSAROU Alexandra
Department of Dermatology, University of Athens, "Andreas Syggros" Hospital
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KOSMADAKI Maria
Department of Dermatology, University of Athens, "Andreas Syggros" Hospital
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KATSAROU Alexandra
Department of Dermatology, University of Athens, "Andreas Syggros" Hospital
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KITSIOU-TZELI Sofia
Department of Medical Genetics, University of Athens, "Aghia Sophia" Children's Hospital
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LEZE Eleni
Department of Medical Genetics, University of Athens, "Aghia Sophia" Children's Hospital
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WILLEMS Patrick
Gendia (GENetic DIAgnostic Network)
関連論文
- New neurocutaneous syndrome with defect in cell trafficking and melanosome pathway : The future challenge
- Combined microdeletions and CHD7 mutation causing severe CHARGE/DiGeorge syndrome : clinical presentation and molecular investigation by array-CGH
- Nevoid basal carcinoma syndrome (Gorlin syndrome) and pronounced androgenic alopecia in a woman with a novel mutation p.Leu1159fsx32 in the PTCH gene