(Q59082330)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3014348%20AND%20SRC:MED&resulttype=core&format=json

8 October 2019

title

Analysis of deletions in DNA from patients with Becker and Duchenne muscular dystrophy (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3014348%20AND%20SRC:MED&resulttype=core&format=json

Duchenne muscular dystrophy

8 October 2019

main subject

1 reference

inferred from title

author

Albert de la Chapelle

60

object named as

de la Chapelle A

1 reference

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8 October 2019

author name string

Kunkel LM

1

1 reference

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8 October 2019

Hejtmancik JF

2

1 reference

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8 October 2019

Caskey CT

3

1 reference

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8 October 2019

Speer A

4

1 reference

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8 October 2019

Monaco AP

5

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8 October 2019

Middlesworth W

6

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8 October 2019

Colletti CA

7

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8 October 2019

Bertelson C

8

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8 October 2019

Müller U

9

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8 October 2019

Bresnan M

10

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8 October 2019

Shapiro F

11

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8 October 2019

Tantravahi U

12

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8 October 2019

Speer J

13

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8 October 2019

Latt SA

14

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8 October 2019

Bartlett R

15

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8 October 2019

Pericak-Vance MA

16

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8 October 2019

Roses AD

17

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8 October 2019

Thompson MW

18

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8 October 2019

Ray PN

19

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8 October 2019

Worton RG

20

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8 October 2019

Fischbeck KH

21

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8 October 2019

Gallano P

22

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8 October 2019

Coulon M

23

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8 October 2019

Duros C

24

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8 October 2019

Boue J

25

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8 October 2019

Junien C

26

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8 October 2019

Chelly J

27

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8 October 2019

Hamard G

28

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8 October 2019

Jeanpierre M

29

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8 October 2019

Lambert M

30

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8 October 2019

Kaplan JC

31

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8 October 2019

Emery A

32

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8 October 2019

Dorkins H

33

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8 October 2019

McGlade S

34

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8 October 2019

Davies KE

35

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8 October 2019

Boehm C

36

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8 October 2019

Arveiler B

37

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8 October 2019

Lemaire C

38

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8 October 2019

Morgan GJ

39

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8 October 2019

Denton MJ

40

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8 October 2019

Amos J

41

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8 October 2019

Bobrow M

42

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8 October 2019

Benham F

43

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8 October 2019

Boswinkel E

44

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8 October 2019

Cole C

45

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8 October 2019

Dubowitz V

46

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8 October 2019

Hart K

47

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8 October 2019

Hodgson S

48

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8 October 2019

Johnson L

49

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8 October 2019

Walker A

50

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8 October 2019

Roncuzzi L

51

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8 October 2019

Ferlini A

52

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8 October 2019

Nobile C

53

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8 October 2019

Romeo G

54

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8 October 2019

Wilcox DE

55

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8 October 2019

Affara NA

56

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8 October 2019

Ferguson-Smith MA

57

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8 October 2019

Lindolf M

58

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8 October 2019

Kaariainen H

59

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8 October 2019

Ionasescu V

61

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8 October 2019

Searby C

62

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8 October 2019

Ionasescu R

63

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8 October 2019

Bakker E

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8 October 2019

van Ommen GJ

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8 October 2019

Pearson PL

66

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8 October 2019

Greenberg CR

67

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8 October 2019

Hamerton JL

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8 October 2019

Wrogemann K

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8 October 2019

Doherty RA

70

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8 October 2019

Polakowska R

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8 October 2019

Hyser C

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8 October 2019

Quirk S

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8 October 2019

Thomas N

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8 October 2019

Harper JF

75

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8 October 2019

Darras BT

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8 October 2019

Francke U

77

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8 October 2019

language of work or name

English

0 references

publication date

1 July 1986

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8 October 2019

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8 October 2019

volume

322

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8 October 2019

page(s)

73-77

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8 October 2019

issue

6074

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https://scigraph.springernature.com/pub.10.1038/322073a0

8 October 2019

exact match

0 references

cites work

Detection of deletions spanning the Duchenne muscular dystrophy locus using a tightly linked DNA segment

1 reference

7 January 2021

Cloning of the breakpoint of an X;21 translocation associated with Duchenne muscular dystrophy.

1 reference

7 January 2021

Molecular Genetics of the Bithorax Complex in Drosophila melanogaster.

1 reference

7 January 2021

Lambda replacement vectors carrying polylinker sequences

1 reference

7 January 2021

Genetic linkage relationships of seven DNA probes with Duchenne and Becker muscular dystrophy

1 reference

7 January 2021

Definitive localization of Becker muscular dystrophy in Xp by linkage to a cluster of DNA polymorphisms (DXS43 and DXS9)

1 reference

7 January 2021

Multipoint linkage analysis of the short arm of the human X chromosome in families with X-linked muscular dystrophy

1 reference

7 January 2021

Isolation of probes detecting restriction fragment length polymorphisms from X chromosome-specific libraries: potential use for diagnosis of Duchenne muscular dystrophy

1 reference

7 January 2021

Specific cloning of DNA fragments absent from the DNA of a male patient with an X chromosome deletion

1 reference

7 January 2021

The genetic linkage map of the human X chromosome

1 reference

7 January 2021

Expression of an X-linked gene from an inactive human X chromosome in mouse-human hybrid cells: further evidence for the noninactivation of the steroid sulfatase locus in man.

1 reference

7 January 2021

Duchenne muscular dystrophy involving translocation of the dmd gene next to ribosomal RNA genes

1 reference

7 January 2021

SERUM ENZYME STUDIES IN MUSCLE DISEASE. III. SERUM CREATINE KINASE ACTIVITY IN RELATIVES OF PATIENTS WITH THE DUCHENNE TYPE OF MUSCULAR DYSTROPHY.

1 reference

7 January 2021

Use of normal daughters' and sisters' creatine kinase levels in estimating heterozygosity in Duchenne muscular dystrophy

1 reference

7 January 2021

Detection of specific sequences among DNA fragments separated by gel electrophoresis

1 reference

7 January 2021

An RFLP detecting single copy X-chromosome fragment, dic56, from Xp22-Xpter [HGM8 assignment no. DXS 143].

1 reference

7 January 2021