(Q28280414)

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Genetic mapping of chronic childhood-onset spinal muscular atrophy to chromosome 5q11.2-13.3

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Genetic mapping of chronic childhood-onset spinal muscular atrophy to chromosome 5q11.2-13.3 (English)

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spinal muscular atrophy

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based on heuristic

inferred from title

muscular atrophy

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author name string

L M Brzustowicz

1

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T Lehner

2

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L H Castilla

3

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G K Penchaszadeh

4

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K C Wilhelmsen

5

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R Daniels

6

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K E Davies

7

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M Leppert

8

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F Ziter

9

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D Wood

10

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language of work or name

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publication date

5 April 1990

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344

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6266

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540-1

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

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https://api.crossref.org/works/10.1038%2F344540A0

7 January 2021

based on heuristic

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Neurogenic muscular atrophy of infancy with prolonged survival. The variable course of Werdnig-Hoffmann Disease

1 reference

https://api.crossref.org/works/10.1038%2F344540A0

7 January 2021

based on heuristic

inferred from DOI database lookup

The genetic identity of acute infantile spinal muscular atrophy

1 reference

https://api.crossref.org/works/10.1038%2F344540A0

7 January 2021

based on heuristic

inferred from DOI database lookup

A clinical and genetic study of spinal muscular atrophy of adult onset: the autosomal recessive form as a discrete disease entity

1 reference

https://api.crossref.org/works/10.1038%2F344540A0

7 January 2021

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INFANTILE MUSCULAR ATROPHY. A PROSPECTIVE STUDY WITH PARTICULAR REFERENCE TO A SLOWLY PROGRESSIVE VARIETY

1 reference

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7 January 2021

based on heuristic

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Chronic generalized spinal muscular atrophy of infancy and childhood. Arrested Werdnig-Hoffman disease

1 reference

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7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2F344540A0

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based on heuristic

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Molecular analysis of Duchenne and Becker muscular dystrophies

1 reference

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Report of the committee on linkage and gene order

1 reference

https://api.crossref.org/works/10.1038%2F344540A0

7 January 2021

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Glucocorticoid receptor maps to the distal long arm of chromosome 5

1 reference

https://api.crossref.org/works/10.1038%2F344540A0

7 January 2021

based on heuristic

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Juvenile spinal muscular atrophy: a new hexosaminidase deficiency phenotype

1 reference

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N-acetyl-beta-hexosaminidase beta locus defect and juvenile motor neuron disease: a case study

1 reference

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Strategies for multilocus linkage analysis in humans

1 reference

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Deletion mapping of DNA markers to a region of chromosome 5 that cosegregates with schizophrenia

1 reference

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based on heuristic

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The gene for familial polyposis coli maps to the long arm of chromosome 5.

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

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