Prenatal diagnosis of alpha 1-antitrypsin deficiency by direct analysis of the mutation site in the gene.

Authors :: Kidd VJ
Golbus MS
Wallace RB
Itakura K
Woo SL
Source :: The New England journal of medicine [N Engl J Med] 1984 Mar 08; Vol. 310 (10), pp. 639-42.
Publication Year :: 1984

Subjects :: Female
Heterozygote
Homozygote
Humans
Male
Nucleic Acid Hybridization
alpha 1-Antitrypsin genetics
Chromosome Mapping
DNA analysis
Mutation
Prenatal Diagnosis methods
alpha 1-Antitrypsin Deficiency

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