Phenotypic variation in the familial atypical multiple mole-melanoma syndrome (FAMMM).-Reference-Cited by-同舟云学术

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Phenotypic variation in the familial atypical multiple mole-melanoma syndrome (FAMMM).

Published:1983-02-01 Issue:1 Volume:20 Page:25-29
ISSN:1468-6244
Container-title:Journal of Medical Genetics
language:en
Short-container-title:Journal of Medical Genetics

Author:

Lynch H T,Fusaro R M,Albano W A,Pester J,Kimberling W J,Lynch J F

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference14 articles.

1. Heritable disorders of connectite tissiue;McKusick, V.A.,1972

2. Cancer genetics;Lynch, H.T.,1976

3. Lynch HT. Genetics, etiology, and human cancer. Prev Med 1980;9:231-43.

4. Breast c ancer genetics;Lynch, H.T.,1981

5. Tumour spectrum in the FAMMM syndrome;Lynch, H.T.; Fusaro, R.M.; Pester, J.;BrJ Cancer,1981

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1. The management of hereditary melanoma, FAMMM syndrome and germline CDKN2A mutations: a narrative review;Australasian Journal of Plastic Surgery;2022-09-30

2. Commentary on Almassalha et al., “The Greater Genomic Landscape: The Heterogeneous Evolution of Cancer”;Cancer Research;2016-09-16

3. Familial atypical multiple mole melanoma (FAMMM) syndrome: history, genetics, and heterogeneity;Familial Cancer;2016-02-18

4. Management of Melanoma Families;Cancers;2010-04-16

5. Hereditary cancer syndrome diagnosis: molecular genetic clues and cancer control;Future Oncology;2007-04

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