DFNB89, a novel autosomal recessive nonsyndromic hearing impairment locus on chromosome 16q21-q23.2. (Q35853567)

10 August 2017

DFNB89, a novel autosomal recessive nonsyndromic hearing impairment locus on chromosome 16q21-q23.2. (English)

1 reference

10 August 2017

1 reference

2

Kwanghyuk Lee

1 reference

10 August 2017

11

Suzanne M Leal

1 reference

10 August 2017

Sulman Basit

1

1 reference

10 August 2017

Rabia Habib

3

1 reference

10 August 2017

Leon Chen

4

1 reference

10 August 2017

Umm-e-Kalsoom

5

1 reference

10 August 2017

Regie Lyn P Santos-Cortez

6

1 reference

10 August 2017

Zahid Azeem

7

1 reference

10 August 2017

Paula Andrade

8

1 reference

10 August 2017

Muhammad Ansar

9

1 reference

10 August 2017

Wasim Ahmad

10

1 reference

10 August 2017

22 December 2010

1 reference

10 August 2017

1 reference

10 August 2017

129

1 reference

10 August 2017

4

1 reference

10 August 2017

379-385

1 reference

https://scigraph.springernature.com/pub.10.1007/s00439-010-0934-0

10 August 2017

0 references

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Cadherin-11 controls otolith assembly: evidence for extracellular cadherin activity

1 reference

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The expression of NOB1 in spiral ganglion cells of guinea pig.

27 July 2018

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27 July 2018

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16q-linked autosomal dominant cerebellar ataxia: a clinical and genetic study.

27 July 2018

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Identification of CRYM as a candidate responsible for nonsyndromic deafness, through cDNA microarray analysis of human cochlear and vestibular tissues

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3312604

Otoancorin, an inner ear protein restricted to the interface between the apical surface of sensory epithelia and their overlying acellular gels, is defective in autosomal recessive deafness DFNB22.

27 July 2018

1 reference

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Merlin--rapid analysis of dense genetic maps using sparse gene flow trees

27 July 2018

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Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23

27 July 2018

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Allegro, a new computer program for multipoint linkage analysis

27 July 2018

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Primer3 on the WWW for general users and for biologist programmers

27 July 2018

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Human cochlear expressed sequence tags provide insight into cochlear gene expression and identify candidate genes for deafness

27 July 2018

1 reference

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PedCheck: a program for identification of genotype incompatibilities in linkage analysis

27 July 2018

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Faster sequential genetic linkage computations

27 July 2018

1 reference

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A simple and efficient non-organic procedure for the isolation of genomic DNA from blood

27 July 2018

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Identification and ultrastructural localization of a calretinin-like calcium-binding protein (protein 10) in the guinea pig and rat inner ear.

27 July 2018

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PCDH15 is expressed in the neurosensory epithelium of the eye and ear and mutant alleles are responsible for both USH1F and DFNB23

27 July 2018

1 reference

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Chromosomal mapping and phenotypic characterization of hereditary otosclerosis linked to the OTSC4 locus.

21 January 2018

1 reference

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An original inner ear neuroepithelial degeneration in a deaf Rottweiler puppy

21 January 2018

1 reference

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Differentiation of inner ear stem cells to functional sensory neurons

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-010-0934-0

Three vertebrate hyaluronan synthases are expressed during mouse development in distinct spatial and temporal patterns

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-010-0934-0

Descent graphs in pedigree analysis: applications to haplotyping, location scores, and marker-sharing statistics

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3312604

E-cadherin in the mature and developing organ of Corti of the mouse

24 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21181198

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

A deletion in the gene encoding sphingomyelin phosphodiesterase 3 (Smpd3) results in osteogenesis and dentinogenesis imperfecta in the mouse

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21181198

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1007/S00439-010-0934-0

1 reference

10 August 2017

1 reference

10 August 2017

1 reference