(Q52125476)

22 April 2018

title

Mapping of the second locus for the Van der Woude syndrome to chromosome 1p34. (English)

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22 April 2018

main subject

Van der Woude syndrome

1 reference

7

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22 April 2018

Juha Kere

11

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22 April 2018

author name string

Koillinen H

1

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22 April 2018

Wong FK

2

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22 April 2018

Rautio J

3

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22 April 2018

Ollikainen V

4

1 reference

22 April 2018

Karsten A

5

1 reference

22 April 2018

Larson O

6

1 reference

22 April 2018

Huggare J

8

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22 April 2018

Lahermo P

9

1 reference

22 April 2018

Larsson C

10

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22 April 2018

publication date

1 October 2001

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22 April 2018

European Journal of Human Genetics

published in

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22 April 2018

volume

9

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22 April 2018

issue

10

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22 April 2018

page(s)

747-752

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22 April 2018

https://scigraph.springernature.com/pub.10.1038/sj.ejhg.5200713

exact match

0 references

cites work

Lower lip sinuses: I. Epidemiology, microforms and transverse sulci

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200713

7 January 2021

The Van der Woude syndrome (dominantly inherited lip pits and clefts).

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200713

7 January 2021

Lip pits and deletion 1q32----41

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200713

7 January 2021

Refinement of the Van der Woude gene location and construction of a 3.5-Mb YAC contig and STS map spanning the critical region in 1q32-q41.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200713

7 January 2021

Evidence for a microdeletion in 1q32-41 involving the gene responsible for Van der Woude syndrome.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200713

7 January 2021

Microdeletions at chromosome bands 1q32-q41 as a cause of Van der Woude syndrome.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200713

7 January 2021

Linkage analysis in a large Brazilian family with van der Woude syndrome suggests the existence of a susceptibility locus for cleft palate at 17p11.2-11.1.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200713

7 January 2021

Clinical and genetic studies of Van der Woude syndrome in Sweden

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200713

7 January 2021

Genetic heterogeneity and exclusion of a modifying locus at 17p11.2-p11.1 in Finnish families with van der Woude syndrome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200713

7 January 2021

Exclusion of candidate genes from a role in cleft lip with or without cleft palate: linkage and association studies

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200713

7 January 2021

A mutation in the gene encoding the alpha 2 chain of the fibril-associated collagen IX, COL9A2, causes multiple epiphyseal dysplasia (EDM2)

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200713

7 January 2021

Identifiers

DOI

10.1038/SJ.EJHG.5200713

1 reference

22 April 2018

PubMed ID

11781685

1 reference

22 April 2018