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Christophe Vincent

Pasteur Institute

10

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Complete exon sequencing of all known Usher syndrome genes greatly improves molecular

2011
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BOR and BO syndromes are allelic defects of EYA1.

1997 European Journal of Human Genetics
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Clustering of Mutations Responsible for Branchio-Oto-Renal (BOR) Syndrome in the Eyes Absent Homologous Region (eyaHR) of EYA1

1997 Human Molecular Genetics
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A human homologue of the Drosophila eyes absent gene underlies branchio-oto-renal (BOR) syndrome and identifies a novel gene family.

1997 Nature Genetics
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A Gene Responsible for a Sensorineural Nonsyndromic Recessive Deafness Maps to Chromosome 2p22–23

1996 Human Molecular Genetics
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Characterization of a Translocation-Associated Deletion Defines the Candidate Region for the Gene Responsible for Branchio-Oto-Renal Syndrome: Volume34,Number 3 (1996), pages 422–425

1996 Genomics
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Characterization of a Translocation-Associated Deletion Defines the Candidate Region for the Gene Responsible for Branchio-Oto-Renal Syndrome

1996 Genomics
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Deficits héréditaires de l'audition chez l'enfant

1995 Annales de l'Institut Pasteur
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A proposed new contiguous gene syndrome on 8q consists of Branchio-Oto-Renal (BOR) syndrome, Duane syndrome, a dominant form of hydrocephalus and trapeze aplasia; implications for the mapping of the BOR gene

1994 Human Molecular Genetics
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Citations (96)