(Q34294793)

1 August 2017

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

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1 August 2017

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Paavola P

1

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1 August 2017

Salonen R

series ordinal

2

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1 August 2017

Weissenbach J

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3

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1 August 2017

Peltonen L

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4

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1 August 2017

language of work or name

English

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publication date

1 October 1995

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1 August 2017

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1 August 2017

11

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1 August 2017

2

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1 August 2017

213-215

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https://scigraph.springernature.com/pub.10.1038/ng1095-213

1 August 2017

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cites work

Linkage disequilibrium utilized to establish a refined genetic position of the Salla disease locus on 6q14-q15

1 reference

https://api.crossref.org/works/10.1038%2FNG1095-213

High-density genetic map of the BRCA1 region of chromosome 17q12-q21

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1095-213

Multiple congenital anomaly caused by an extra autosome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1095-213

The 1993-94 Généthon human genetic linkage map

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1095-213

The Meckel syndrome: clinicopathological findings in 67 patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1095-213

7 January 2021

The Meckel syndrome in Finland: epidemiologic and genetic aspects

1 reference

https://api.crossref.org/works/10.1038%2FNG1095-213

7 January 2021

High incidence of Meckel's syndrome in Gujarati Indians

1 reference

https://api.crossref.org/works/10.1038%2FNG1095-213

7 January 2021

Meckel syndrome and neural tube defects in Kuwait

1 reference

https://api.crossref.org/works/10.1038%2FNG1095-213

7 January 2021

A simple sequence repeat polymorphism at the human growth hormone locus

1 reference

https://api.crossref.org/works/10.1038%2FNG1095-213

7 January 2021

Dominant mutation of the murine Hox-2.2 gene results in developmental abnormalities

1 reference

https://api.crossref.org/works/10.1038%2FNG1095-213

7 January 2021

Ectopic expression of Hoxb-8 causes duplication of the ZPA in the forelimb and homeotic transformation of axial structures.

1 reference

https://api.crossref.org/works/10.1038%2FNG1095-213

7 January 2021

The murine Hox-2 cluster of homeo box containing genes maps distal on chromosome 11 near the tail-short ( Ts ) locus

1 reference

https://api.crossref.org/works/10.1038%2FNG1095-213

7 January 2021

A dinucleotide repeat polymorphism at the HOX2B locus

1 reference

https://api.crossref.org/works/10.1038%2FNG1095-213

7 January 2021

A genetic linkage map of chromosome 17

1 reference

https://api.crossref.org/works/10.1038%2FNG1095-213

7 January 2021

Microsatellite polymorphism in the human platelet glycoprotein IIIa gene (GP3A) on chromosome 17

1 reference

https://api.crossref.org/works/10.1038%2FNG1095-213

7 January 2021

Strategies for multilocus linkage analysis in humans

1 reference

https://api.crossref.org/works/10.1038%2FNG1095-213

7 January 2021

Meckel syndrome: what are the minimum diagnostic criteria?

1 reference

https://api.crossref.org/works/10.1038%2FNG1095-213

7 January 2021

Identifiers

DOI

10.1038/NG1095-213

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Dimensions Publication ID

1 August 2017

1014918086

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Fatcat ID

release_eatvslbcjbbuvjkpwl56oesn6m

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/eatvslbcjbbuvjkpwl56oesn6m

24 November 2022

mapped directly with Wikidata item

1 reference