(Q24680303)

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Homozygous mutations in fibroblast growth factor 3 are associated with a new form of syndromic deafness characterized by inner ear agenesis, microtia, and microdontia

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17236138%20AND%20SRC:MED&resulttype=core&format=json

24 December 2019

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Homozygous mutations in fibroblast growth factor 3 are associated with a new form of syndromic deafness characterized by inner ear agenesis, microtia, and microdontia (English)

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17236138%20AND%20SRC:MED&resulttype=core&format=json

24 December 2019

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based on heuristic

inferred from title

1 reference

based on heuristic

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1 reference

based on heuristic

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1

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17236138%20AND%20SRC:MED&resulttype=core&format=json

24 December 2019

4

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Europe PubMed Central

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24 December 2019

8

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24 December 2019

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Burcu Oztürk Hişmi

2

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24 December 2019

Suat Fitoz

3

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24 December 2019

Filiz Başak Cengiz

5

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Europe PubMed Central

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24 December 2019

Asli Sirmaci

6

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17236138%20AND%20SRC:MED&resulttype=core&format=json

24 December 2019

Idil Aslan

7

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17236138%20AND%20SRC:MED&resulttype=core&format=json

24 December 2019

E Berrin Yüksel-Konuk

9

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Europe PubMed Central

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24 December 2019

Seda Taşir Yilmaz

10

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Europe PubMed Central

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24 December 2019

Oztan Yasun

11

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Europe PubMed Central

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24 December 2019

Nejat Akar

12

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Europe PubMed Central

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24 December 2019

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publication date

27 December 2006

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Europe PubMed Central

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24 December 2019

American Journal of Human Genetics

1 reference

Europe PubMed Central

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24 December 2019

80

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24 December 2019

2

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17236138%20AND%20SRC:MED&resulttype=core&format=json

24 December 2019

338-344

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17236138%20AND%20SRC:MED&resulttype=core&format=json

24 December 2019

Temporal bone computed tomography findings in bilateral sensorineural hearing loss

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1785350

7 April 2017

Mice homozygous for a targeted disruption of the proto-oncogene int-2 have developmental defects in the tail and inner ear

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1785350

7 April 2017

The int-2 proto-oncogene is responsible for induction of the inner ear

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1785350

7 April 2017

FGF8 initiates inner ear induction in chick and mouse

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1785350

7 April 2017

Requirements for FGF3 and FGF10 during inner ear formation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1785350

7 April 2017

Fgf3 and Fgf10 are required for mouse otic placode induction

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1785350

7 April 2017

Interactive visual analysis of SNP data for rapid autozygosity mapping in consanguineous families

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1785350

28 September 2017

Newborn hearing screening--a silent revolution

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1785350

28 September 2017

LADD syndrome is caused by FGF10 mutations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1785350

28 September 2017

Mutations in different components of FGF signaling in LADD syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1785350

28 September 2017

Expression of the FGF-related proto-oncogene int-2 during gastrulation and neurulation in the mouse

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1785350

28 September 2017

Expression pattern of the FGF-related proto-oncogene int-2 suggests multiple roles in fetal development.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1785350

30 May 2018

Michel's anomaly, type I microtia and microdontia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1785350

30 May 2018

A new method for autozygosity mapping using single nucleotide polymorphisms (SNPs) and EXCLUDEAR.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1785350

28 November 2018

Use of laboratory evaluation and radiologic imaging in the diagnostic evaluation of children with sensorineural hearing loss.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1785350

28 November 2018

easyLINKAGE: a PERL script for easy and automated two-/multi-point linkage analyses

1 reference

https://pubmed.ncbi.nlm.nih.gov/17236138

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Induction of inner ear fate by FGF3

1 reference

https://pubmed.ncbi.nlm.nih.gov/17236138

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17236138%20AND%20SRC:MED&resulttype=core&format=json

24 December 2019

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17236138%20AND%20SRC:MED&resulttype=core&format=json

24 December 2019

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17236138%20AND%20SRC:MED&resulttype=core&format=json

24 December 2019

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