(Q38362075)

English

Molecular analysis of the SMN and NAIP genes in Spanish spinal muscular atrophy (SMA) families and correlation between number of copies of cBCD541 and SMA phenotype

scientific article

In more languages

default for all languages

No label defined

No description defined

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

2 September 2017

Molecular analysis of the SMN and NAIP genes in Spanish spinal muscular atrophy (SMA) families and correlation between number of copies of cBCD541 and SMA phenotype (English)

1 reference

Europe PubMed Central

PubMed publication ID

2 September 2017

spinal muscular atrophy

1 reference

based on heuristic

inferred from title

muscular atrophy

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

author name string

Velasco E

1

1 reference

Europe PubMed Central

PubMed publication ID

2 September 2017

Valero C

2

1 reference

Europe PubMed Central

PubMed publication ID

2 September 2017

Valero A

3

1 reference

Europe PubMed Central

PubMed publication ID

2 September 2017

Moreno F

4

1 reference

Europe PubMed Central

PubMed publication ID

2 September 2017

Hernández-Chico C

5

1 reference

Europe PubMed Central

PubMed publication ID

2 September 2017

language of work or name

1 reference

based on heuristic

inferred from title

publication date

1 February 1996

1 reference

Europe PubMed Central

PubMed publication ID

2 September 2017

Human Molecular Genetics

1 reference

Europe PubMed Central

PubMed publication ID

2 September 2017

5

1 reference

Europe PubMed Central

PubMed publication ID

2 September 2017

2

1 reference

Europe PubMed Central

PubMed publication ID

2 September 2017

257-263

1 reference

Europe PubMed Central

PubMed publication ID

2 September 2017

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

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F5.2.257

21 January 2018

A contig of non-chimaeric YACs containing the spinal muscular atrophy gene in 5q13.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F5.2.257

21 January 2018

Construction of a yeast artificial chromosome contig spanning the spinal muscular atrophy disease gene region

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F5.2.257

21 January 2018

A YAC Contig of the Region Containing the Spinal Muscular Atrophy Gene (SMA): Identification of an Unstable Region

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F5.2.257

21 January 2018

Refined physical map of the spinal muscular atrophy gene (SMA) region at 5q13 based on YAC and cosmid contiguous arrays.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F5.2.257

21 January 2018

High resolution physical map of the region surrounding the spinal muscular atrophy gene

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F5.2.257

21 January 2018

Mapping of retrotransposon sequences in the unstable region surrounding the spinal muscular atrophy locus in 5q13.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F5.2.257

21 January 2018

Identification and characterization of a spinal muscular atrophy-determining gene

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F5.2.257

21 January 2018

Expressed cadherin pseudogenes are localized to the critical region of the spinal muscular atrophy gene

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F5.2.257

21 January 2018

The gene for neuronal apoptosis inhibitory protein is partially deleted in individuals with spinal muscular atrophy

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F5.2.257

21 January 2018

A novel cDNA detects homozygous microdeletions in greater than 50% of type I spinal muscular atrophy patients

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F5.2.257

21 January 2018

Deletions in the survival motor neuron gene on 5q13 in autosomal recessive spinal muscular atrophy.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F5.2.257

21 January 2018

Cell death during development of the nervous system

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F5.2.257

21 January 2018

The head involution defective gene of Drosophila melanogaster functions in programmed cell death

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F5.2.257

21 January 2018

Splice junctions, branch point sites, and exons: sequence statistics, identification, and applications to genome project

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F5.2.257

21 January 2018

Genomic rearrangements in childhood spinal muscular atrophy: linkage disequilibrium with a null allele

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F5.2.257

21 January 2018

A simple salting out procedure for extracting DNA from human nucleated cells

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F5.2.257

21 January 2018

Dinucleotide repeat polymorphisms at the D5S1356, D5S1357 and D7S1480 loci

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F5.2.257

21 January 2018

Gene for chronic proximal spinal muscular atrophies maps to chromosome 5q

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F5.2.257

21 January 2018

Genetic homogeneity between acute and chronic forms of spinal muscular atrophy

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F5.2.257

21 January 2018

Mapping of acute (type I) spinal muscular atrophy to chromosome 5q12-q14

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F5.2.257

21 January 2018

Identifiers

10.1093/HMG/5.2.257

1 reference

Europe PubMed Central

PubMed publication ID

2 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

2 September 2017

ResearchGate publication ID

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q38362075&oldid=1755802526"