Branchio-oto-renal syndrome (BOR): novel mutations in the EYA1 gene, and a review of the mutational genetics of BOR. (Q37065180)

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1 January 2020

title

Branchio-oto-renal syndrome (BOR): novel mutations in the EYA1 gene, and a review of the mutational genetics of BOR (English)

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1 January 2020

7

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1 January 2020

Richard J Smith

9

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1 January 2020

5

Cor W R J Cremers

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1 January 2020

author name string

Dana J Orten

1

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1 January 2020

Stephanie M Fischer

2

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1 January 2020

Jessica L Sorensen

3

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1 January 2020

Uppala Radhakrishna

4

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1 January 2020

Henri A M Marres

6

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1 January 2020

Katherine O Welch

8

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1 January 2020

William J Kimberling

10

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1 January 2020

publication date

1 April 2008

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1 January 2020

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1 January 2020

volume

29

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1 January 2020

issue

4

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1 January 2020

page(s)

537-544

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Clustering of mutations responsible for branchio-oto-renal (BOR) syndrome in the eyes absent homologous region (eyaHR) of EYA1

1 January 2020

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Identification of two major loci that suppress hearing loss and cochlear dysmorphogenesis in Eya1bor/bor mice

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7 January 2021

Townes-Brocks syndrome: twenty novel SALL1 mutations in sporadic and familial cases and refinement of the SALL1 hot spot region

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7 January 2021

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7 January 2021