Prenatal diagnosis and carrier detection of Duchenne muscular dystrophy with closely linked RFLPs (Q69859264)

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6 October 2019

title

Prenatal diagnosis and carrier detection of Duchenne muscular dystrophy with closely linked RFLPs (English)

1 reference

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Duchenne muscular dystrophy

6 October 2019

main subject

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E Bakker

1

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6 October 2019

M H Hofker

2

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6 October 2019

N Goor

3

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6 October 2019

J L Mandel

4

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6 October 2019

K Wrogemann

5

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6 October 2019

K E Davies

6

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6 October 2019

L M Kunkel

7

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6 October 2019

H F Willard

8

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6 October 2019

W A Fenton

9

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6 October 2019

L Sandkuyl

10

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6 October 2019

language of work or name

English

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publication date

1 March 1985

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6 October 2019

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6 October 2019

volume

1

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6 October 2019

issue

8430

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6 October 2019

page(s)

655-658

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The biochemical identification of the carrier state in X-linked recessive (Duchenne) muscular dystrophy

6 October 2019

cites work

1 reference

https://api.crossref.org/works/10.1016/S0140-6736(85)91325-X

7 January 2021

Linkage relationship of a cloned DNA sequence on the short arm of the X chromosome to Duchenne muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016/S0140-6736(85)91325-X

7 January 2021

Linkage analysis of two cloned DNA sequences flanking the Duchenne muscular dystrophy locus on the short arm of the human X chromosome

1 reference

https://api.crossref.org/works/10.1016/S0140-6736(85)91325-X

7 January 2021

Expression of an X-linked muscular dystrophy in a female due to translocation involving Xp21 and non-random inactivation of the normal X chromosome

1 reference

https://api.crossref.org/works/10.1016/S0140-6736(85)91325-X

7 January 2021

Further evidence for Xp21 location of Duchenne muscular dystrophy (DMD) locus: X;9 translocation in a female with DMD.

1 reference

https://api.crossref.org/works/10.1016/S0140-6736(85)91325-X

7 January 2021

Carrier detection in Duchenne muscular dystrophy by use of cloned DNA sequences

1 reference

https://api.crossref.org/works/10.1016/S0140-6736(85)91325-X

7 January 2021

Regional localization on the human X of DNA segments cloned from flow sorted chromosomes

1 reference

https://api.crossref.org/works/10.1016/S0140-6736(85)91325-X

7 January 2021

Structure and Expression of a Complementary DNA for the Nuclear Coded Precursor of Human Mitochondrial Ornithine Transcarbamylase

1 reference

https://api.crossref.org/works/10.1016/S0140-6736(85)91325-X

7 January 2021

Gene for OTC: characterisation and linkage to Duchenne muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016/S0140-6736(85)91325-X

7 January 2021

First trimester chromosomal analysis of complex structural rearrangements with RHA banding on chorionic villi

1 reference

https://api.crossref.org/works/10.1016/S0140-6736(85)91325-X

7 January 2021

Detection of specific sequences among DNA fragments separated by gel electrophoresis

1 reference

https://api.crossref.org/works/10.1016/S0140-6736(85)91325-X

7 January 2021

Unusual scarcity of restriction site polymorphism in the human thyroglobulin gene. A linkage study suggesting autosomal dominance of a defective thyroglobulin allele

1 reference

https://api.crossref.org/works/10.1016/S0140-6736(85)91325-X

7 January 2021

DNA probes in Duchenne muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016/S0140-6736(85)91325-X

7 January 2021

Serum creatine kinase activity and carrier status for duchenne muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016/S0140-6736(85)91325-X

7 January 2021

10.1016/S0140-6736(85)91325-X

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2858615 AND SRC:MED&resulttype=core&format=json

6 October 2019

1 reference