(Q42933670)

11 November 2017

Prenatal diagnosis of spinal muscular atrophy: clinical experience and molecular genetics of SMN gene analysis in 36 cases. (English)

1 reference

11 November 2017

spinal muscular atrophy

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1 reference

Mahmoud Shekari Khaniani

series ordinal

1

1 reference

11 November 2017

Sima Mansoori Derakhshan

series ordinal

2

1 reference

11 November 2017

Shamsei Abasalizadeh

series ordinal

3

1 reference

11 November 2017

language of work or name

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1 July 2013

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Journal of prenatal medicine

11 November 2017

1 reference

11 November 2017

7

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11 November 2017

3

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11 November 2017

32-34

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Spinal muscular atrophy: clinical spectrum and genetic mutations in Pakistani children

11 November 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3808942

Spinal muscular atrophy: a clinical and research update

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3808942

Spinal muscular atrophy disease: a literature review for therapeutic strategies

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3808942

Deletions in the survival motor neuron gene in Iranian patients with spinal muscular atrophy

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3808942

Molecular analysis of survival motor neuron gene in 338 suspicious children patients with spinal muscular atrophy

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3808942

Molecular diagnosis of spinal muscular atrophy in Egyptians

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3808942

Molecular prenatal diagnosis of autosomal recessive spinal muscular atrophies using quantification polymerase chain reaction.

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3808942

Prenatal diagnosis of spinal muscular atrophy in Macedonian families

16 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3808942

Molecular analysis of the spinal muscular atrophy and neuronal apoptosis inhibitory protein genes in Saudi patients with spinal muscular atrophy

16 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3808942

Genetic diagnosis of Werdnig-Hoffmann disease: a problem for application to prenatal diagnosis.

16 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3808942

Parents of children with spinal muscular atrophy are not obligate carriers: Carrier testing is important for reproductive decision-making

16 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3808942

Molecular analysis of the SMN1 and NAIP genes in Iranian patients with spinal muscular atrophy

1 December 2018

1 reference

12 December 2020

Prenatal prediction of spinal muscular atrophy by SMN deletion analysis

1 reference

12 December 2020

Deletion analyses of SMN1 and NAIP genes in Malaysian spinal muscular atrophy patients

1 reference

12 December 2020

Molecular analysis of the SMN and NAIP genes in Iranian spinal muscular atrophy patients

1 reference

12 December 2020

Identifiers

1 reference

11 November 2017

PubMed publication ID

24175014

1 reference