Prenatal diagnosis of alpha 1-antitrypsin deficiency by restriction fragment length polymorphisms, and comparison with oligonucleotide probe analysis (Q69887574)

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scientific article published on 01 October 1986

Language	Label	Description	Also known as
English	Prenatal diagnosis of alpha 1-antitrypsin deficiency by restriction fragment length polymorphisms, and comparison with oligonucleotide probe analysis	scientific article published on 01 October 1986

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scholarly article

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2876232%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

Prenatal diagnosis of alpha 1-antitrypsin deficiency by restriction fragment length polymorphisms, and comparison with oligonucleotide probe analysis (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2876232%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

alpha-1-antitrypsin deficiency

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J F Hejtmancik

1

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6 October 2019

R N Sifers

2

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Europe PubMed Central

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6 October 2019

P A Ward

3

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6 October 2019

S Harris

4

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6 October 2019

T Mansfield

5

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6 October 2019

D W Cox

6

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6 October 2019

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publication date

1 October 1986

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6 October 2019

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2876232%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

2

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6 October 2019

8510

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6 October 2019

767-770

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6 October 2019

alpha1-antitrypsin deficiency (first of two parts).

1 reference

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Smoking, lung function, and alpha 1-antitrypsin deficiency.

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7 January 2021

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Liver Disease in Alpha1-Antitrypsin Deficiency Detected by Screening of 200,000 Infants

1 reference

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7 January 2021

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Four-year-old children with alpha 1-antitrypsin deficiency. Clinical follow-up and parental attitudes towards neonatal screening.

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7 January 2021

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Liver disease associated with alpha1-antitrypsin deficiency in childhood

1 reference

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7 January 2021

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Prenatal diagnosis of alpha 1-antitrypsin deficiency by analysis of fetal blood obtained at fetoscopy

1 reference

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

1 reference

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7 January 2021

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Evaluation of "at risk" alpha 1-antitrypsin genotype SZ with synthetic oligonucleotide gene probes

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7 January 2021

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Allele-specific hybridization using oligonucleotide probes of very high specific activity: discrimination of the human beta A- and beta S-globin genes

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7 January 2021

based on heuristic

inferred from DOI database lookup

Prenatal diagnosis for alpha 1-antitrypsin deficiency

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

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7 January 2021

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Analysis of human Y-chromosome-specific reiterated DNA in chromosome variants

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7 January 2021

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Polymorphism of DNA sequence adjacent to human beta-globin structural gene: relationship to sickle mutation

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

1 reference

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7 January 2021

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Identifiers

10.1016/S0140-6736(86)90297-7

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2876232%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2876232%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

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