(Q35249899)

7 August 2017

title

A gene for arthrogryposis multiplex congenita neuropathic type is linked to D5S394 on chromosome 5qter (English)

1 reference

7 August 2017

6

Rotter JI

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7 August 2017

Shohat M

1

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7 August 2017

Lotan R

2

1 reference

7 August 2017

Magal N

3

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7 August 2017

Shohat T

4

1 reference

7 August 2017

Fischel-Ghodsian N

5

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7 August 2017

Jaber L

7

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7 August 2017

language of work or name

English

0 references

publication date

1 November 1997

1 reference

American Journal of Human Genetics

7 August 2017

published in

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7 August 2017

volume

61

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7 August 2017

issue

5

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7 August 2017

page(s)

1139-1143

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Survival motor neuron gene deletion in the arthrogryposis multiplex congenita-spinal muscular atrophy association

7 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1716024

Strategies for multilocus linkage analysis in humans

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1716024

Arthrogryposis multiplex congenita. Report of two cases of a radicular type with familial incidence.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1716024

Homozygosity mapping: a way to map human recessive traits with the DNA of inbred children

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1716024

Marked parental consanguinity as a cause for increased major malformations in an Israeli Arab community

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1716024

Cerebral lesions in arthrogryposis multiplex congenita.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1716024

Arthrogryposis multiplex congenita

26 September 2018

1 reference

12 December 2020

Arthrogryposis multiplex congenita: twenty-three cases in an Arab kindred

1 reference

12 December 2020

Recurrence risks in a consecutive series of congenitally malformed children dying in the perinatal period

1 reference

12 December 2020

Arthrogryposis multiplex congenita in an Arab kindred: update

1 reference

12 December 2020

[Anatomical study of a case of congenital and familial multiple arthrogryposis]

1 reference

12 December 2020

Identifiers

DOI

10.1086/301598

1 reference

7 August 2017

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7 August 2017

1 reference