(Q72888821)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8355122%20AND%20SRC:MED&resulttype=core&format=json

30 October 2019

title

Hereditary motor-sensory neuropathy (Charcot-Marie-Tooth disease) with nerve deafness: a new variant (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8355122%20AND%20SRC:MED&resulttype=core&format=json

30 October 2019

1 reference

1 reference

O P Hamiel

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8355122%20AND%20SRC:MED&resulttype=core&format=json

30 October 2019

A Raas-Rothschild

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8355122%20AND%20SRC:MED&resulttype=core&format=json

30 October 2019

M Upadhyaya

3

1 reference

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30 October 2019

M Frydman

4

1 reference

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30 October 2019

I Sarova-Pinhas

5

1 reference

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30 October 2019

N Brand

6

1 reference

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30 October 2019

J H Passwell

7

1 reference

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30 October 2019

language of work or name

English

0 references

publication date

1 September 1993

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8355122%20AND%20SRC:MED&resulttype=core&format=json

The Journal of Pediatrics

30 October 2019

published in

1 reference

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30 October 2019

volume

123

1 reference

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30 October 2019

issue

3

1 reference

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30 October 2019

page(s)

431-434

1 reference

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Hereditary motor and sensory neuropathies

30 October 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2805%2981752-4

Abnormal auditory evoked potentials in hereditary motor-sensory neuropathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2805%2981752-4

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2805%2981752-4

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2805%2981752-4

Auditory function in hereditary motor and sensory neuropathy (Charcot-Marie-Tooth disease).

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2805%2981752-4

Genetic linkage evidence for heterogeneity in Charcot-Marie-Tooth neuropathy (HMSN type I).

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2805%2981752-4

Estimation of the size of the chromosome 17p11.2 duplication in Charcot-Marie-Tooth neuropathy type 1a (CMT1a). HMSN Collaborative Research Group

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2805%2981752-4

Charcot-Marie-Tooth disease type 1a (CMT1a): evidence for trisomy of the region p11.2 of chromosome 17 in south Wales families

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2805%2981752-4

Familial opticoacoustic nerve degeneration and polyneuropathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2805%2981752-4

X-linked motor-sensory neuropathy type-II with deafness and mental retardation: a new disorder.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2805%2981752-4

Expansion of an unstable DNA region and phenotypic variation in myotonic dystrophy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2805%2981752-4

10.1016/S0022-3476(05)81752-4

7 January 2021

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8355122%20AND%20SRC:MED&resulttype=core&format=json

30 October 2019

1 reference