Hereditary genodermatoses with cancer predisposition - Test2 - elhamkhani - TriplyDB

Hereditary genodermatoses with cancer predisposition

Hereditary genodermatoses with cancer predisposition

http://www.wikidata.org/entity/Q30470596

about

Risk of subsequent malignant neoplasms in long-term hereditary retinoblastoma survivors after chemotherapy and radiotherapy Fallopian tube correlates of ovarian serous borderline tumors.Multiple skin neoplasms in subjects under 40 years of age in Goiania, Brazil

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P2860

Hereditary genodermatoses with cancer predisposition

http://www.wikidata.org/entity/Q30470596

description

2010 nî lūn-bûn

@nan

2010 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2010 թվականի հոտեմբերին հրատարակված գիտական հոդված

@hy

2010年の論文

@ja

2010年学术文章

@wuu

2010年学术文章

@zh-cn

2010年学术文章

@zh-hans

2010年学术文章

@zh-my

2010年学术文章

@zh-sg

2010年學術文章

@yue

name

Hereditary genodermatoses with cancer predisposition

@ast

Hereditary genodermatoses with cancer predisposition

@en

type

label

Hereditary genodermatoses with cancer predisposition

@ast

Hereditary genodermatoses with cancer predisposition

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prefLabel

Hereditary genodermatoses with cancer predisposition

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Hereditary genodermatoses with cancer predisposition

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P356

J.HOC.2010.06.003

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Hematology / Oncology Clinics of North America

P1476

Hereditary genodermatoses with cancer predisposition

@en

P2093

Alisa M Goldstein

http://www.w3.org/2001/XMLSchema#string

Margaret A Tucker

http://www.w3.org/2001/XMLSchema#string

Meg R Gerstenblith

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P2860

The protein product of the neurofibromatosis type 1 gene is expressed at highest abundance in neurons, Schwann cells, and oligodendrocytes

Most germ-line mutations in the nevoid basal cell carcinoma syndrome lead to a premature termination of the PATCHED protein, and no genotype-phenotype correlations are evident

Interaction between hamartin and tuberin, the TSC1 and TSC2 gene products

Activating Smoothened mutations in sporadic basal-cell carcinoma

Mutations of the human homolog of Drosophila patched in the nevoid basal cell carcinoma syndrome

Mutational analysis in a cohort of 224 tuberous sclerosis patients indicates increased severity of TSC2, compared with TSC1, disease in multiple organs

Comprehensive mutation analysis of TSC1 and TSC2-and phenotypic correlations in 150 families with tuberous sclerosis.

Xeroderma pigmentosum, trichothiodystrophy and Cockayne syndrome: a complex genotype-phenotype relationship

Renal cystic disease in tuberous sclerosis: role of the polycystic kidney disease 1 gene

Identification of PATCHED mutations in medulloblastomas by direct sequencing

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885-906

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scholarly article

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10.1016/J.HOC.2010.06.003

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5

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24

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2010-10-01T00:00:00Z

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46147942

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20816579

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3276063

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