Gorlin Syndrome in a type IV-skin person with a novel PTCH1 mutation: Case report and literature review
Nevoid basal cell carcinoma syndrome (NBCCS), or Gorlin Syndrome, is an autosomal dominant multisystem disorder, characterized by multiple developmental abnormalities and inactivation germline mutations in the human homolog of the patched (PTCH) gene. We are presenting a case of NBCCS in a skin type...
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| Asıl Yazarlar: | , |
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| Materyal Türü: | Kitap |
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Wolters Kluwer Medknow Publications,
2016-01-01T00:00:00Z.
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Connect to this object online.3rd Floor Main Library
| Yer Numarası: |
A1234.567 |
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| Kopya Bilgisi 1 | Kütüphanede |