(Q33679760)

28 July 2017

title

Associated malformations in the family of a patient with Meckel syndrome: heterozygous expression? (English)

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28 July 2017

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Gulati R

1

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28 July 2017

Phadke SR

series ordinal

2

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28 July 2017

Agarwal SS

series ordinal

3

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28 July 2017

language of work or name

English

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publication date

1 November 1997

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Journal of Medical Genetics

28 July 2017

published in

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28 July 2017

volume

34

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28 July 2017

issue

11

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28 July 2017

page(s)

937-938

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Polydactyly in a carrier of the gene for the Meckel syndrome

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=1051125

The locus for Meckel syndrome with multiple congenital anomalies maps to chromosome 17q21-q24.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051125

The Meckel syndrome: clinicopathological findings in 67 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=1051125

Genetics of the Meckel syndrome (dysencephalia splanchnocystica)

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051125

The Meckel syndrome with limited expression in relatives

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051125

21 June 2018

Identifiers

DOI

10.1136/JMG.34.11.937

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28 July 2017

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28 July 2017

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