4.6 Article

Characterization of individuals at high risk of developing melanoma in Latin America: bases for genetic counseling in melanoma

Related references

Note: Only part of the references are listed.
Review Oncology

Genetics of familial melanoma: 20 years after CDKN2A

Lauren G. Aoude et al.

PIGMENT CELL & MELANOMA RESEARCH (2015)

Article Dermatology

MC1R gene variants and sporadic malignant melanoma susceptibility in the Canary Islands population

Elizabeth Cordoba-Lanus et al.

ARCHIVES OF DERMATOLOGICAL RESEARCH (2014)

Article Oncology

Germline CDKN2A mutations in Brazilian patients of hereditary cutaneous melanoma

Alexandre Leon Ribeiro de Avila et al.

FAMILIAL CANCER (2014)

Article Oncology

Melanoma Genetic Counseling and Test Reporting Improve Screening Adherence Among Unaffected Carriers 2 Years Later

Lisa G. Aspinwall et al.

CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION (2013)

Article Dermatology

Monitoring Patients with Multiple Nevi

Susana Puig et al.

DERMATOLOGIC CLINICS (2013)

Article Dermatology

Genetic variations of patients with familial or multiple melanoma in Southern Brazil

T. C. Grazziotin et al.

JOURNAL OF THE EUROPEAN ACADEMY OF DERMATOLOGY AND VENEREOLOGY (2013)

Article Oncology

Evaluation of PAX3 genetic variants and nevus number

Zighereda Ogbah et al.

PIGMENT CELL & MELANOMA RESEARCH (2013)

Article Dermatology

Genetic counseling in melanoma

Celia Badenas et al.

DERMATOLOGIC THERAPY (2012)

Article Genetics & Heredity

CDKN2A is the main susceptibility gene in Italian pancreatic cancer families

Paola Ghiorzo et al.

JOURNAL OF MEDICAL GENETICS (2012)

Article Dermatology

Melanomas Detected in a Follow-up Program Compared With Melanomas Referred to a Melanoma Unit

Gabriel Salerni et al.

ARCHIVES OF DERMATOLOGY (2011)

Article Oncology

Association of MC1R Variants and Host Phenotypes With Melanoma Risk in CDKN2A Mutation Carriers: A GenoMEL Study

F. Demenais et al.

JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE (2010)

Article Dermatology

CDKN2A mutations in melanoma families from Uruguay

A. L. Borges et al.

BRITISH JOURNAL OF DERMATOLOGY (2009)

Article Oncology

Melanocortin receptor 1 variants and melanoma risk: A study of 2 European populations

Dominique Scherer et al.

INTERNATIONAL JOURNAL OF CANCER (2009)

Article Oncology

Final Version of 2009 AJCC Melanoma Staging and Classification

Charles M. Balch et al.

JOURNAL OF CLINICAL ONCOLOGY (2009)

Review Dermatology

Selection criteria for genetic assessment of patients with familial melanoma

Sancy A. Leachman et al.

JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY (2009)

Article Oncology

MC1R variants, melanoma and red hair color phenotype: A meta-analysis

Sara Raimondi et al.

INTERNATIONAL JOURNAL OF CANCER (2008)

Article Dermatology

Clinical and molecular characterization of patients at risk for hereditary melanoma in Southern Brazil

Patricia Ashton-Prolla et al.

JOURNAL OF INVESTIGATIVE DERMATOLOGY (2008)

Article Genetics & Heredity

Comprehensive evaluation of allele frequency differences of MC1R variants across populations

Meg R. Gerstenblith et al.

HUMAN MUTATION (2007)

Article Genetics & Heredity

Features associated with germline CDKN2A mutations: a GenoMEL study of melanoma-prone families from three continents

Alisa M. Goldstein et al.

JOURNAL OF MEDICAL GENETICS (2007)

Article Oncology

Cancer in 15-to 29-year-olds by primary site

Archie Bleyer et al.

ONCOLOGIST (2006)

Article Biology

The P48T germline mutation and polymorphism in the CDKN2A gene of patients with melanoma

J Huber et al.

BRAZILIAN JOURNAL OF MEDICAL AND BIOLOGICAL RESEARCH (2006)

Article Oncology

Role of the CDKN2A locus in patients with multiple primary melanomas

S Puig et al.

JOURNAL OF CLINICAL ONCOLOGY (2005)

Article Genetics & Heredity

A single genetic origin for the G101W CDKN2A mutation in 20 melanoma-prone families

P Ciotti et al.

AMERICAN JOURNAL OF HUMAN GENETICS (2000)