DNA restriction fragments associated with alpha 1-antitrypsin indicate a single origin for deficiency allele PI Z. (Q53813578)

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English	DNA restriction fragments associated with alpha 1-antitrypsin indicate a single origin for deficiency allele PI Z.	scientific article

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

20 May 2018

http://europepmc.org/abstract/MED/2989709

DNA restriction fragments associated with alpha 1-antitrypsin indicate a single origin for deficiency allele PI Z. (English)

1 reference

Europe PubMed Central

PubMed publication ID

20 May 2018

http://europepmc.org/abstract/MED/2989709

author name string

Cox DW

1

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Europe PubMed Central

PubMed publication ID

20 May 2018

http://europepmc.org/abstract/MED/2989709

Woo SL

2

1 reference

Europe PubMed Central

PubMed publication ID

20 May 2018

http://europepmc.org/abstract/MED/2989709

Mansfield T

3

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Europe PubMed Central

PubMed publication ID

20 May 2018

http://europepmc.org/abstract/MED/2989709

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1 July 1985

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Europe PubMed Central

PubMed publication ID

20 May 2018

http://europepmc.org/abstract/MED/2989709

1 reference

Europe PubMed Central

PubMed publication ID

20 May 2018

http://europepmc.org/abstract/MED/2989709

316

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Europe PubMed Central

PubMed publication ID

20 May 2018

http://europepmc.org/abstract/MED/2989709

6023

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Europe PubMed Central

PubMed publication ID

20 May 2018

http://europepmc.org/abstract/MED/2989709

79-81

1 reference

Europe PubMed Central

PubMed publication ID

20 May 2018

http://europepmc.org/abstract/MED/2989709

Genes for immunoglobulin heavy chains and for α1-antitrypsin are localized to specific regions of chromosome 14q

1 reference

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7 January 2021

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Sequence homology and structural comparison between the chromosomal human alpha 1-antitrypsin and chicken ovalbumin genes

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α1-Antitrypsin deficiency detection by direct analysis of the mutation in the gene

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Complete sequence of the cDNA for human .alpha.1-antitrypsin and the gene for the S variant

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7 January 2021

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Amino acid substitution Glu→Lys in α1-antitrypsin PiZ

1 reference

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7 January 2021

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Molecular abnormality of human alpha1-antitrypsin variant (Pi-ZZ) associated with plasma activity deficiency

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Antenatal diagnosis of sickle-cell anaemia by D.N.A. analysis of amniotic-fluid cells

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Evolution of sickle variant gene

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Nonrandom association of polymorphic restriction sites in the β-globin gene cluster

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Restriction fragment length polymorphisms associated with immunoglobulin C gamma genes reveal linkage disequilibrium and genomic organization

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Prenatal diagnosis for alpha 1-antitrypsin deficiency

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Association of severe rheumatoid arthritis with heterozygosity for alpha 1-antitrypsin deficiency

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Identifiers

10.1038/316079A0

1 reference

Europe PubMed Central

PubMed publication ID

20 May 2018

http://europepmc.org/abstract/MED/2989709

Dimensions Publication ID

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

20 May 2018

http://europepmc.org/abstract/MED/2989709

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