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Nele Hilgert

Showing results (11-20 of 15) with videos related to

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American Journal of Human Genetics|August 16, 2006
A new autosomal recessive form of Stickler syndrome is caused by a mutation in the COL9A1 geneGuy Van Camp, Rikkert L Snoeckx, Nele Hilgert, et al.
Human Genetics|July 30, 2010
Multiple enhancers located in a 1-Mb region upstream of POU3F4 promote expression during inner ear development and may be required for hearingSilvia Naranjo, Krysta Voesenek, Elisa de la Calle-Mustienes, et al.
American Journal of Medical Genetics. Part A|April 13, 2011
Two Iranian families with a novel mutation in GJB2 causing autosomal dominant nonsyndromic hearing lossNiloofar Bazazzadegan, Abraham M Sheffield, Masoomeh Sobhani, et al.
European Journal of Human Genetics : EJHG|November 6, 2008
Phenotypic variability of patients homozygous for the GJB2 mutation 35delG cannot be explained by the influence of one major modifier geneNele Hilgert, Matthew J Huentelman, Ashley Q Thorburn, et al.
American Journal of Human Genetics|December 29, 2005
GJB2 mutations and degree of hearing loss: a multicenter studyRikkert L Snoeckx, Patrick L M Huygen, Delphine Feldmann, et al.
Pageof 2

Showing results (11-20 of 15) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 15 results.
American Journal of Human Genetics|August 16, 2006
A new autosomal recessive form of Stickler syndrome is caused by a mutation in the COL9A1 geneGuy Van Camp, Rikkert L Snoeckx, Nele Hilgert, et al.
Human Genetics|July 30, 2010
Multiple enhancers located in a 1-Mb region upstream of POU3F4 promote expression during inner ear development and may be required for hearingSilvia Naranjo, Krysta Voesenek, Elisa de la Calle-Mustienes, et al.
American Journal of Medical Genetics. Part A|April 13, 2011
Two Iranian families with a novel mutation in GJB2 causing autosomal dominant nonsyndromic hearing lossNiloofar Bazazzadegan, Abraham M Sheffield, Masoomeh Sobhani, et al.
European Journal of Human Genetics : EJHG|November 6, 2008
Phenotypic variability of patients homozygous for the GJB2 mutation 35delG cannot be explained by the influence of one major modifier geneNele Hilgert, Matthew J Huentelman, Ashley Q Thorburn, et al.
American Journal of Human Genetics|December 29, 2005
GJB2 mutations and degree of hearing loss: a multicenter studyRikkert L Snoeckx, Patrick L M Huygen, Delphine Feldmann, et al.
Pageof 2