C. Cremers

Clinical aspects of an autosomal dominantly inherited hearing impairment linked to the DFNA60 locus on chromosome 2q23.1–2q23.3

H. Kremer, R. Pennings, R. Collin, 2013, Hearing Research.

A novel locus for autosomal recessive nonsyndromic hearing impairment, DFNB63, maps to chromosome 11q13.2–q13.4

C. Cremers, H. Brunner, H. Kremer, 2007, Journal of Molecular Medicine.

JUVENILE DIABETES MELLITUS, OPTIC ATROPHY, HEARING LOSS, DIABETES INSIPIDUS, ATONIA OF THE URINARY TRACT AND BLADDER, AND OTHER ABNORMALITIES (WOLFRAM SYNDROME)

C. Cremers, A. Pinckers, P. Wijdeveld, 1977, Acta paediatrica Scandinavica. Supplement.

A novel D458V mutation in the SANS PDZ binding motif causes atypical Usher syndrome

H. G. Brunner, C. Cremers, S. Nabuurs, 2005, Journal of Molecular Medicine.

Detection of Rare Nonsynonymous Variants in TGFB1 in Otosclerosis Patients

C. Cremers, E. Fransen, G. Van Camp, 2009, Annals of human genetics.

A mutation in the gamma actin 1 (ACTG1) gene causes autosomal dominant hearing loss (DFNA20/26)

E. Krieger, E. van Wijk, H. Kremer, 2003, Journal of medical genetics.

CDH23 mutation and phenotype heterogeneity: a profile of 107 diverse families with Usher syndrome and nonsyndromic deafness.

J. W. Askew, W. Reardon, H. Kremer, 2002, American journal of human genetics.

Clinical Report on the L95P Mutation in a Dutch Family with Paraganglioma

H. Kremer, L. Hoefsloot, F. Joosten, 2002, Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology.

A new locus for otosclerosis, OTSC10, maps to chromosome 1q41–44

E. Fransen, G. Van Camp, I. Schrauwen, 2011, Clinical genetics.

Neo‐oval window technique and myringo‐chorda‐vestibulopexy in the BOR syndrome

C. Cremers, H. Brunner, H. Marres, 1993, The Laryngoscope.

Four novel TMC1 (DFNB7/DFNB11) mutations in Turkish patients with congenital autosomal recessive nonsyndromic hearing loss

H. Brunner, H. Kremer, F. Cremers, 2005, Human mutation.

Analysis of DNA elements that modulate myosin VIIA expression in humans

S. Jacobson, M. D. Weston, P. M. Kelley, 1999, Human mutation.

Familial aggregation of tinnitus: a European multicentre study.

T. Wienker, H. Kremer, D. Stephens, 2007, B-ENT.

Two frequent missense mutations in Pendred syndrome.

E. Green, C. Cremers, N. Dietrich, 1998, Human molecular genetics.