Direct gene analysis of chorionic villi: A possible technique for first-trimester antenatal diagnosis of haemoglobinopathies (Q72511033)

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27 October 2019

title

Direct gene analysis of chorionic villi: A possible technique for first-trimester antenatal diagnosis of haemoglobinopathies (English)

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27 October 2019

author name string

R. Williamson

1

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8 August 2023

J. Eskdale

2

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8 August 2023

D. V. Coleman

3

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8 August 2023

M. Niazi

4

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8 August 2023

F. E. Loeffler

5

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8 August 2023

B. M. Modell

6

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8 August 2023

language of work or name

English

0 references

publication date

1 November 1981

1 reference

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27 October 2019

21 November 1981

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=6118574

full work available at URL

8 August 2023

https://api.elsevier.com/content/article/PII:S0140673681905833?httpAccept=text/xml

1 reference

10.1016/S0140-6736(81)90583-3

DOI

https://api.crossref.org/works/10.1016/S0140-6736(81)90583-3

https://api.elsevier.com/content/article/PII:S0140673681905833?httpAccept=text/plain

8 August 2023

1 reference

10.1016/S0140-6736(81)90583-3

DOI

https://api.crossref.org/works/10.1016/S0140-6736(81)90583-3

8 August 2023

1 reference

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27 October 2019

volume

2

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27 October 2019

issue

8256

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27 October 2019

page(s)

1125-1127

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The severe form of alpha thalassaemia is caused by a haemoglobin gene deletion

27 October 2019

cites work

1 reference

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7 January 2021

Gene deletion as the cause of α thalassaemia: Genetic lesion in homozygous α thalassaemia (hydrops fetalis)

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7 January 2021

Insertion of synthetic copies of human globin genes into bacterial plasmids

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7 January 2021

Isolation and partial sequence of recombinant plasmids containing human α-, β- and γ-globin cDNA fragments

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7 January 2021

Prenatal diagnosis of alpha-thalassemia. Clinical application of molecular hybridization

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7 January 2021

Application of endonuclease mapping to the analysis and prenatal diagnosis of thalassemias caused by globin-gene deletion

1 reference

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7 January 2021

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

1 reference

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7 January 2021

Model for antenatal diagnosis of β-thalassaemia and other monogenic disorders by molecular analysis of linked DNA polymorphisms

1 reference

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7 January 2021

An intron nucleotide sequence variant in a cloned β+-thalassaemia globin gene

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7 January 2021

Direct identification of sickle cell anemia by blot hybridization

1 reference

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7 January 2021

Prenatal diagnosis of hemoglobinopathies. A review of 15 cases

1 reference

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7 January 2021

10.1016/S0140-6736(81)90583-3

Identifiers

DOI

1 reference

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27 October 2019

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