PRENATAL DIAGNOSIS OF α1-ANTITRYPSIN DEFICIENCY BY RESTRICTION FRAGMENT LENGTH POLYMORPHISMS, AND COMPARISON WITH OLIGONUCLEOTIDE PROBE ANALYSIS-Reference-Cited by-同舟云学术

PRENATAL DIAGNOSIS OF α1-ANTITRYPSIN DEFICIENCY BY RESTRICTION FRAGMENT LENGTH POLYMORPHISMS, AND COMPARISON WITH OLIGONUCLEOTIDE PROBE ANALYSIS

Published:1986-10 Issue:8510 Volume:328 Page:767-770
ISSN:0140-6736
Container-title:The Lancet
language:en
Short-container-title:The Lancet

Author:

Hejtmancik J.F.,Ward P.A.,Mansfield T.,Sifers R.N.,Harris S.,Cox D.W.

Publisher

Elsevier BV

Subject

General Medicine

Reference25 articles.

1. Studies in alpha 1-antitrypsin deficiency;Eriksson;Acta Med Scand,1965

2. Natural history and life expectancy in severe alpha 1-antitrypsin deficiency, PI Z;Larsson;Acta Med Scand,1978

3. Cirrhosis associated with alpha 1-antitrypsin deficiency: a previously unrecognized inherited disorder;Sharp;J Lab Clin Med,1969

4. Protease inhibitors in patients with chronic obstructive pulmonary disease: the alpha 1-antitrypsin heterozygote controversy;Cox;Am Rev Resp Dis,1976

5. Mass screening of newborn Swedish infants for alpha 1-antitrypsin deficiency;Laurell;Am J Hum Genet,1975

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