Publications by authors named "Kris Flothmann"

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A novel Z-score-based method to analyze candidate genes for age-related hearing impairment.
Erik Fransen, Lut Van Laer, Nele Lemkens, Goele Caethoven, Kris Flothmann

Ear Hear· April 2004

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Mutational spectrum of the WFS1 gene in Wolfram syndrome, nonsyndromic hearing impairment, diabetes mellitus, and psychiatric disease.
Kim Cryns, Theru A Sivakumaran, Jody M W Van den Ouweland, Ronald J E Pennings, Cor W R J Cremers, Kris Flothmann

Hum Mutat· October 2003

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Progression of low-frequency sensorineural hearing loss (DFNA6/14-WFS1).
Ronald J E Pennings, Steven J H Bom, Kim Cryns, Kris Flothmann, Patrick L M Huygen

Arch Otolaryngol Head Neck Surg· April 2003

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Is DFNA5 a susceptibility gene for age-related hearing impairment?
Lut Van Laer, Anita L DeStefano, Richard H Myers, Kris Flothmann, Sofie Thys

Eur J Hum Genet· December 2002

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Mutations in the WFS1 gene that cause low-frequency sensorineural hearing loss are small non-inactivating mutations.
Kim Cryns, Markus Pfister, Ronald J E Pennings, Steven J H Bom, Kris Flothmann

Hum Genet· May 2002

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Vestibular dysfunction in the epistatic circler mouse is caused by phenotypic interaction of one recessive gene and three modifier genes.
Kim Cryns, Michiel P Van Spaendonck, Kris Flothmann, Arjan M van Alphen, Paul H Van De Heyning

Genome Res· April 2002

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The ABCA4 2588G>C Stargardt mutation: single origin and increasing frequency from South-West to North-East Europe.
Alessandra Maugeri, Kris Flothmann, Nadine Hemmrich, Sofie Ingvast, Paula Jorge

Eur J Hum Genet· March 2002

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