Cowden syndrome: report of a large family with macrocephaly and increased severity of signs in subsequent generations-Reference-Cited by-同舟云学术

Cowden syndrome: report of a large family with macrocephaly and increased severity of signs in subsequent generations

Published:2008-04-23 Issue:6 Volume:44 Page:281-286
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:

Author:

Hanssen A. M. N.,Werquin H.,Suys E.,Fryns J. P.

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1993.tb03901.x/fullpdf

Reference40 articles.

1. Multiple hamartoma syndrome with endometrial carcinoma and the sign of Leser-Trelat;Aylesworth;Arch Dermatol,1982

2. Sindrome di Cowden. A proposito di due casi familiari;Barba;G Ital Dermatol Venereol,1988

3. Cowden's disease;Bardenstein;Ophthalmology,1988

4. Maladie de Cowden (6e cas français). Efficacité de l'étretinate sur les manifestations cutanées et digestives;Bruhière;Gastroenterol Clin Biol,1986

5. Cowden disease. Report of two additional cases;Burnett;Br J Dermatol,1975

Cited by 37 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Hereditary Cancer Syndromes: Risk Assessment and Genetic Counseling;Holland‐Frei Cancer Medicine;2022-10-21

2. Sindrome dello spettro autistico e macrocefalia: la sindrome di Cowden;Medico e Bambino Pagine elettroniche;2022-05-31

3. Genomics of human congenital hydrocephalus;Child's Nervous System;2021-07-07

4. Approach to von Hippel Lindau, Cowden disease, and other inherited conditions;Neuro-Oncology for the Clinical Neurologist;2021

5. Hereditary Cancer Syndromes: Risk Assessment and Genetic Counseling;Holland‐Frei Cancer Medicine;2019-12-06