(Q28292269)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8841199%20AND%20SRC:MED&resulttype=core&format=json

19 October 2019

title

Gene mapping in Gypsies identifies a novel demyelinating neuropathy on chromosome 8q24 (English)

1 reference

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19 October 2019

10

1 reference

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19 October 2019

Alan H. Bittles

18

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8841199%20AND%20SRC:MED&resulttype=core&format=json

19 October 2019

author name string

Kalaydjieva L

1

1 reference

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19 October 2019

Hallmayer J

2

1 reference

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19 October 2019

Chandler D

3

1 reference

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19 October 2019

Savov A

4

1 reference

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19 October 2019

Nikolova A

5

1 reference

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19 October 2019

Angelicheva D

6

1 reference

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19 October 2019

King RH

7

1 reference

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19 October 2019

Ishpekova B

8

1 reference

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19 October 2019

Honeyman K

9

1 reference

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19 October 2019

Shmarov A

11

1 reference

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19 October 2019

Petrova J

12

1 reference

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19 October 2019

Turnev I

13

1 reference

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19 October 2019

Hristova A

14

1 reference

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19 October 2019

Moskov M

15

1 reference

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19 October 2019

Stancheva S

16

1 reference

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19 October 2019

Petkova I

17

1 reference

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19 October 2019

Georgieva V

19

1 reference

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19 October 2019

Middleton L

20

1 reference

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19 October 2019

Thomas PK

21

1 reference

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19 October 2019

language of work or name

English

0 references

publication date

1 October 1996

1 reference

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19 October 2019

1 reference

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19 October 2019

volume

14

1 reference

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19 October 2019

page(s)

214-217

1 reference

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19 October 2019

issue

2

1 reference

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https://scigraph.springernature.com/pub.10.1038/ng1096-214

19 October 2019

exact match

0 references

cites work

A manic depressive history.

1 reference

https://api.crossref.org/works/10.1038%2FNG1096-214

Disease gene mapping in isolated human populations: the example of Finland

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1096-214

7 January 2021

Genome screening by searching for shared segments: mapping a gene for benign recurrent intrahepatic cholestasis

1 reference

https://api.crossref.org/works/10.1038%2FNG1096-214

7 January 2021

A Dejerine-Sottas neuropathy family with a gene mapped on chromosome 8

1 reference

https://api.crossref.org/works/10.1038%2FNG1096-214

7 January 2021

Autosomal recessive inheritance of Charcot-Marie-Tooth disease associated with sensorineural deafness

1 reference

https://api.crossref.org/works/10.1038%2FNG1096-214

7 January 2021

The 1993-94 Généthon human genetic linkage map

1 reference

https://api.crossref.org/works/10.1038%2FNG1096-214

7 January 2021

A comprehensive human linkage map with centimorgan density. Cooperative Human Linkage Center (CHLC)

1 reference

https://api.crossref.org/works/10.1038%2FNG1096-214

7 January 2021

Avoiding recomputation in linkage analysis.

1 reference

https://api.crossref.org/works/10.1038%2FNG1096-214

7 January 2021

The VITESSE algorithm for rapid exact multilocus linkage analysis via genotype set-recoding and fuzzy inheritance

1 reference

https://api.crossref.org/works/10.1038%2FNG1096-214

7 January 2021

Identifiers

DOI

10.1038/NG1096-214

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8841199%20AND%20SRC:MED&resulttype=core&format=json

19 October 2019

1 reference