H. Kunst

Variable degrees of hearing impairment in a Dutch DFNX4 (DFN6) family

H. Kremer, R. Pennings, N. Weegerink, 2011, Hearing Research.

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.

Genotype phenotype correlations for hearing impairment: Approaches to management

H. Kremer, L. Hoefsloot, I. Feenstra, 2014, Clinical genetics.

Ear and hearing problems in relation to karyotype in children with Turner syndrome

C. Cremers, R. Pennings, H. Timmers, 2011, Hearing Research.

Further audiovestibular characterization of DFNB77, caused by deleterious variants in LOXHD1, and investigation into the involvement of Fuchs corneal dystrophy

A. Beynon, H. Kremer, C. Hoyng, 2018, Clinical genetics.

Audiometric characteristics of two Dutch families with non-ocular Stickler syndrome (COL11A2)

A. Snik, R. Leuwer, L. Hoefsloot, 2012, Hearing Research.

Fine mapping of autosomal dominant nonsyndromic hearing impairment DFNA21 to chromosome 6p24.1‐22.3

C. Cremers, H. Kremer, F. Cremers, 2005, American journal of medical genetics. Part A.

Audiological Characteristics of Some Affected Members of a Dutch DFNA13/COL11A2 Family

C. Cremers, A. Bosman, P. Huygen, 2004, The Annals of otology, rhinology, and laryngology.

Autosomal dominant inherited non-syndromic sensorineural hearing impairment : phenotype and genotype correlations of DFNA2-DFNA13-DFNA14-DFNA21

H. Kunst, 1999 .

Heterozygous missense variants of LMX1A lead to nonsyndromic hearing impairment and vestibular dysfunction

M. Huynen, A. Beynon, P. Lichtner, 2018, Human Genetics.

Audiometric characteristics of a Dutch family with Muckle-Wells syndrome

A. Snik, H. Kremer, L. Hoefsloot, 2011, Hearing Research.

Progressive hereditary hearing impairment caused by a MYO6 mutation resembles presbyacusis

A. Snik, A. Beynon, H. Kremer, 2013, Hearing Research.

Vestibular function and temporal bone imaging in DFNB1

A. Beynon, H. Kremer, R. Pennings, 2015, Hearing Research.

Features of autosomal recessive non‐syndromic hearing impairment: a review to serve as a reference

H. Kremer, R. Pennings, P. Huygen, 2016, Clinical otolaryngology : official journal of ENT-UK ; official journal of Netherlands Society for Oto-Rhino-Laryngology & Cervico-Facial Surgery.