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Linda Peters

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Linda M Peters; RA Fridell; Erich T Boger; T B San Agustin; Anne C Madeo; Andrew J Griffith; Thomas B Friedman; R J Morell
A locus for autosomal dominant progressive non-syndromic hearing loss, DFNA27, is on chromosome 4q12-13.1.
Linda M Peters; Inna A Belyantseva; Ayala Lagziel; James F Battey; Thomas B Friedman; Robert J Morell
Signatures from tissue-specific MPSS libraries identify transcripts preferentially expressed in the mouse inner ear.
Linda M Peters; David W Anderson; Andrew J Griffith; Kenneth M Grundfast; Theresa B San Agustin; Anne C Madeo; Thomas B Friedman; Robert J Morell
Mutation of a transcription factor, TFCP2L3, causes progressive autosomal dominant hearing loss, DFNA28.

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2008: Linda M Peters; RA Fridell; Erich T Boger; T B San Agustin; Anne C Madeo; Andrew J Griffith; Thomas B Friedman; R J Morell
A locus for autosomal dominant progressive non-syndromic hearing loss, DFNA27, is on chromosome 4q12-13.1.
Clinical genetics 2008;73(4):367-72.
2007: Linda M Peters; Inna A Belyantseva; Ayala Lagziel; James F Battey; Thomas B Friedman; Robert J Morell
Signatures from tissue-specific MPSS libraries identify transcripts preferentially expressed in the mouse inner ear.
Genomics 2007;89(2):197-206.
2002: Linda M Peters; David W Anderson; Andrew J Griffith; Kenneth M Grundfast; Theresa B San Agustin; Anne C Madeo; Thomas B Friedman; Robert J Morell
Mutation of a transcription factor, TFCP2L3, causes progressive autosomal dominant hearing loss, DFNA28.
Human molecular genetics 2002;11(23):2877-85.
2002: Kiyoto Kurima; Linda M Peters; Yandan Yang; Sheikh Amer Riazuddin; Zubair M Ahmed; Sadaf Naz; Deidre Arnaud; Stacy Drury; Jianhong Mo; Tomoko Makishima; Manju Ghosh; P S N Menon; Dilip Deshmukh; Carole Oddoux; Harry Ostrer; Shaheen Khan; Sheikh Riazuddin; Prescott L Deininger; Lori L Hampton; Susan L Sullivan; James F Battey; Bronya J B Keats; Edward R Wilcox; Thomas B Friedman; Andrew J Griffith
Dominant and recessive deafness caused by mutations of a novel gene, TMC1, required for cochlear hair-cell function.
Nature genetics 2002;30(3):277-84.
2001: Julie M Bork; Linda M Peters; S Riazuddin; Steven L Bernstein; Z M Ahmed; Seth L Ness; R Polomeno; Arabandi Ramesh; M Schloss; C R Srisailpathy; S Wayne; S Bellman; D Desmukh; Zubair M Ahmed; Shaheen N Khan; V M Kaloustian; XC Li; Anil K Lalwani; Sheikh Amer Riazuddin; Maria Bitner-Glindzicz; Walter E Nance; Xue Zhong Liu; G Wistow; Richard J H Smith; Andrew J Griffith; Edward R Wilcox; Thomas B Friedman; Robert J Morell
Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23.
American journal of human genetics 2001;68(1):26-37.