NewEPCAMfounder deletion in Polish population-Reference-Cited by-同舟云学术

NewEPCAMfounder deletion in Polish population

Published:2017-08-03 Issue:6 Volume:92 Page:649-653
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:Clin Genet

Author:

Dymerska D.¹,Gołębiewska K.¹,Kuświk M.¹,Rudnicka H.¹,Scott R.J.¹²³,Billings R.³,Pławski A.⁴⁵,Boruń P.⁴,Siołek M.⁵⁶,Kozak-Klonowska B.⁵⁶,Szwiec M.⁶⁷,Kilar E.⁷⁸,Huzarski T.¹,Byrski T.¹,Lubiński J.¹,Kurzawski G.¹

Affiliation:

1. Hereditary Cancer Center, Department of Genetics and Pathology; Pomeranian Medical University; Szczecin Poland

2. Discipline of Medical Genetics; University of Newcastle; Newcastle Australia

3. Division of Genetics; John Hunter Hospital; Newcastle Australia

4. Institute of Human Genetics; Polish Academy of Sciences; Poznań Poland

5. Department of General, Endocrinological Surgery and Gastroenterological Oncology; Poznan University of Medical Sciences; Poznań Poland

6. Holy Cross Cancer Center, Counselling Unit; Kielce Poland

7. Regional Oncology Center, Counselling Unit; Opole Poland

8. Regional Oncology Center, Counselling Unit; Świdnica Poland

Funder

Disease Model & Mechanisms traveling fellowship by the Company of Biologists

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/cge.13026/fullpdf

Reference26 articles.

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5. Identification of a founder BRCA2 mutation in Sardinia;Pisano;Br J Cancer,2000

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