Genetic Heterogeneity of Familial Primary Cutaneous Amyloidosis: Lack of Evidence for Linkage with the Chromosome 10 Pericentromeric Region in Chinese Families-Reference-Cited by-同舟云学术

Genetic Heterogeneity of Familial Primary Cutaneous Amyloidosis: Lack of Evidence for Linkage with the Chromosome 10 Pericentromeric Region in Chinese Families

Published:1996-07 Issue:1 Volume:107 Page:30-33
ISSN:0022-202X
Container-title:Journal of Investigative Dermatology
language:en
Short-container-title:Journal of Investigative Dermatology

Author:

Lee Ding-Dar,Huang Jiun-Yu,Wong Chu-Kwan,Gagel Robert F.,Tsai Shih-Feng

Publisher

Elsevier BV

Subject

Cell Biology,Dermatology,Molecular Biology,Biochemistry

Reference32 articles.

1. Identification of the Cys634→Tyr mutation of the RET protooncogene in a pedigree with multiple endocrine neoplasia type 2A and localized cutaneous lichen amyloidosis;Ceccherini;J Endocrinol Invest,1994

2. Cutaneous lesions associated with multiple endocrine neoplasms type 2A (Sipple's syndrome);Chabre;An early clinical marker. Presse Med,1992

3. Mutarions in the RET proto-oncogene are associated with MEN 2A and FMTC;Donis-Keller;Hum Mol Genet,1993

4. Primary localized cutaneous amyloidosis and familial medullary thyroid carcinoma;Ferrer;Clin Endocrinol,1991

5. Cutaneous lichen amyloidosis and familial medullary thyroid carcinoma (Letter);Ferrer;Ann Intern Med,1989

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