(Q58183900)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1721895%20AND%20SRC:MED&resulttype=core&format=json

17 September 2019

title

The duplication in Charcot-Marie-Tooth disease type 1a spans at least 1100 kb on chromosome 17p11.2. (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1721895%20AND%20SRC:MED&resulttype=core&format=json

Charcot-Marie-Tooth disease type 1A

17 September 2019

main subject

1 reference

9

1 reference

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17 September 2019

author name string

J E Hoogendijk

1

1 reference

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17 September 2019

G W Hensels

2

1 reference

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17 September 2019

I Zorn

3

1 reference

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17 September 2019

L Valentijn

4

1 reference

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17 September 2019

E A Janssen

5

1 reference

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17 September 2019

M de Visser

6

1 reference

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17 September 2019

D F Barker

7

1 reference

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17 September 2019

B W Ongerboer de Visser

8

1 reference

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17 September 2019

P A Bolhuis

10

1 reference

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17 September 2019

publication date

1 December 1991

1 reference

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17 September 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1721895%20AND%20SRC:MED&resulttype=core&format=json

17 September 2019

volume

88

1 reference

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17 September 2019

issue

2

1 reference

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17 September 2019

page(s)

215-218

1 reference

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https://scigraph.springernature.com/pub.10.1007/bf00206075

17 September 2019

exact match

0 references

cites work

Direct assignment of the human beta B2 and beta B3 crystallin genes to 22q11.2----q12: markers for neurofibromatosis 2

1 reference

12 December 2020

Multipoint linkage analysis in neurofibromatosis type I: an international collaboration

1 reference

12 December 2020

A genetic map of human chromosome 17p

1 reference

12 December 2020

The clinical features of hereditary motor and sensory neuropathy types I and II

1 reference

12 December 2020

Prevalence of hereditary motor and sensory neuropathy in Cantabria

1 reference

12 December 2020

Gene for von Recklinghausen neurofibromatosis is in the pericentromeric region of chromosome 17

1 reference

12 December 2020

Separation of chromosomal DNA molecules from yeast by orthogonal-field-alternation gel electrophoresis

1 reference

12 December 2020

Separation of large DNA molecules by contour-clamped homogeneous electric fields

1 reference

12 December 2020

Genetic linkage of hereditary motor and sensory neuropathy type I (Charcot-Marie-Tooth disease) to markers of chromosomes 1 and 17

1 reference

12 December 2020

DNA duplication associated with Charcot-Marie-Tooth disease type 1A

1 reference

12 December 2020

Linkage of Charcot-Marie-Tooth neuropathy type 1a to chromosome 17

1 reference

12 December 2020

Multilocus linkage analysis in humans: detection of linkage and estimation of recombination

1 reference

12 December 2020

Duplication in chromosome 17p11.2 in Charcot-Marie-Tooth neuropathy type 1a (CMT 1a)

1 reference

12 December 2020

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

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00206075

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1721895%20AND%20SRC:MED&resulttype=core&format=json

17 September 2019

1 reference