ΔF508 GENE DELETION IN CYSTIC FIBROSIS IN SOUTHERN EUROPE-Reference-Cited by-同舟云学术

ΔF508 GENE DELETION IN CYSTIC FIBROSIS IN SOUTHERN EUROPE

Published:1989-12 Issue:8676 Volume:334 Page:1404
ISSN:0140-6736
Container-title:The Lancet
language:en
Short-container-title:The Lancet

Author:

Estivill X.,Casals T.,Morral N.,Chillon M.,Bosch A.,Nunes V.,Gasparini P.,Seia A.,Pignatti P.F.,Novelli G.,Dallapiccola B.,Fernandez E.,Benitez J.,Williamson R.

Publisher

Elsevier BV

Subject

General Medicine

Reference7 articles.

1. Identification of the cystic fibrosis gene: genetic analysis;Kerem;Science,1989

2. Prenatal detection of major cystic fibrosis mutation;Halley;Lancet,1989

3. First-trimester prenatal diagnosis of cystic fibrosis by direct gene probing;McIntosh;Lancet,1989

4. Patterns of polymorphism and linkage disequilibrium for cystic fibrosis;Estivill;Genonucs,1987

5. Linkage disequilibrium between cystic fibrosis and linked DNA markers in Italian families: a collaborative study;Estivill;Am J Hum Genet,1988

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