The differential diagnosis of familial lentiginosis syndromes-Reference-Cited by-同舟云学术

The differential diagnosis of familial lentiginosis syndromes

Published:2011-05-03 Issue:3 Volume:10 Page:481-490
ISSN:1389-9600
Container-title:Familial Cancer
language:en
Short-container-title:Familial Cancer

Author:

Lodish Maya B.,Stratakis Constantine A.

Publisher

Springer Science and Business Media LLC

Subject

Cancer Research,Genetics (clinical),Oncology,Genetics

Link

http://link.springer.com/content/pdf/10.1007/s10689-011-9446-x.pdf

Reference97 articles.

1. Fitzpatrick TB, Wolff K (2008) Fitzpatrick’s dermatology in general medicine, 7th edn. McGraw-Hill, New York

2. Marsh DJ, Stratakis CA (2001) Hamartoma and lentiginosis syndromes: clinical and molecular aspects. Front Horm Res 28:167–213

3. Stratakis CA (2000) Genetics of Peutz-Jeghers syndrome, Carney complex and other familial lentiginoses. Horm Res 54:334–343

4. Bauer AJ, Stratakis CA (2005) The lentiginoses: cutaneous markers of systemic disease and a window to new aspects of tumourigenesis. J Med Genet 42:801–810

5. Peutz JLA (1921) Very remarkable case of familial polyposis of mucous membrane of intestinal tract and nasopharynx accompanied by peculiar pigmentations of skin and mucous membrane. (Dutch). Nederl Maandschr Geneesk 10:134–146

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