Segregation analysis of chronic childhood spinal muscular atrophy (Q33588379)

28 July 2017

title

Segregation analysis of chronic childhood spinal muscular atrophy (English)

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28 July 2017

main subject

spinal muscular atrophy

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1 reference

Pearn J

1

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28 July 2017

language of work or name

English

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publication date

1 December 1978

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Journal of Medical Genetics

28 July 2017

published in

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28 July 2017

volume

15

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28 July 2017

issue

6

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28 July 2017

page(s)

418-423

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Tuberous sclerosis: a genetic study

28 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013755

Genetics of childhood spinal muscular atrophy

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013755

The nosology of the spinal muscular atrophies

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013755

The genetic identity of acute infantile spinal muscular atrophy

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013755

Acute Werdnig-Hoffmann disease: acute infantile spinal muscular atrophy

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013755

A clinical and genetic study of chronic proximal spinal muscular atrophy

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013755

International collaborative study of the spinal muscular atrophies. Part 2. Analysis of genetic data

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013755

A genetic study of subacute and chronic spinal muscular atrophy in childhood. A nosological analysis of 124 index patients

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013755

Infantile muscular atrophy

21 June 2018

1 reference

12 December 2020

Benign spinal muscular atrophy arising in childhood and adolescence

1 reference

12 December 2020

Spinal muscular atrophy type II. A separate genetic and clinical entity from type I (Werdnig-Hoffmann disease) and type 3 (Kugelberg-Welander disease)

1 reference

12 December 2020

Progressive Spinal Muscular Atrophy with Onset in Infancy or Early Childhood

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12 December 2020

Identifiers

PMC publication ID

1013755

1 reference

28 July 2017

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