(Q50490317)

14 March 2018

title

Further evidence for linkage of low-mid frequency hearing impairment to the candidate region on chromosome 4p16.3. (English)

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14 March 2018

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3

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author name string

Brodwolf S

1

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14 March 2018

Böddeker IR

2

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14 March 2018

Rausch P

4

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14 March 2018

Kunz J

5

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14 March 2018

publication date

1 August 2001

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14 March 2018

published in

Clinical Genetics

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14 March 2018

volume

60

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14 March 2018

page(s)

155-160

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14 March 2018

issue

2

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14 March 2018

A gene for autosomal dominant nonsyndromic hereditary hearing impairment maps to 4p16.3

cites work

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.600211.X

Nonsyndromic deafness DFNA1 associated with mutation of a human homolog of the Drosophila gene diaphanous

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.600211.X

Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results

21 January 2018

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https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.600211.X

The gene for an inherited form of deafness maps to chromosome 5q31

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.600211.X

Familial low frequency hearing loss

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.600211.X

Msx1 deficient mice exhibit cleft palate and abnormalities of craniofacial and tooth development

21 January 2018

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https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.600211.X

A human MSX1 homeodomain missense mutation causes selective tooth agenesis

21 January 2018

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https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.600211.X

The ancient regulatory-protein family of WD-repeat proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.600211.X

A gene upregulated in the acoustically damaged chick basilar papilla encodes a novel WD40 repeat protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.600211.X

Genes necessary for directed axonal elongation or fasciculation in C. elegans

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.600211.X

Cloning and characterization of the mouse collapsin response mediator protein-1, Crmp1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.600211.X

Autosomal dominant non-syndromal low-frequency sensorineural hearing impairment linked to chromosome 4p16 (DFNA14): statistical analysis of hearing threshold in relation to age and evaluation of vestibulo-ocular functions.

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.600211.X

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1034/J.1399-0004.2001.600211.X

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14 March 2018

PubMed ID

11553051

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14 March 2018