D. Hoover

发表

Splice-altering variant in COL11A1 as a cause of nonsyndromic hearing loss DFNA37

J. W. Askew, Katherine R. Smith, M. Bahlo, 2018, Genetics in Medicine.

Tietz syndrome (hypopigmentation/deafness) caused by mutation ofMITF

Shelley D. Smith, P. M. Kelley, J. Kenyon, 2000, Journal of medical genetics.

Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.

H. Rehm, C. Cremers, C. Möller, 1998, Science.

Fluctuating sensorineural hearing loss associated with enlarged vestibular aqueduct maps to 7q31, the region containing the Pendred gene.

W. Kimberling, S. Usami, S. Abe, 1999, American journal of medical genetics.

Genetic heterogeneity of Usher syndrome: analysis of 151 families with Usher type I.

S. Jacobson, C. Cremers, W. Reardon, 2000, American journal of human genetics.

Refinement of the 6p21.3 quantitative trait locus influencing dyslexia: linkage and association analyses

B. Pennington, R. Olson, J. Defries, 2004, Human Genetics.

Reading Disability and Chromosome 6p21.3

J. W. Askew, R. Olson, Shelley D. Smith, 2001, Journal of learning disabilities.

Phylogenetic analysis of mitochondrial DNA in Japanese pedigrees of sensorineural hearing loss associated with the A1555G mutation

W. Kimberling, S. Horai, S. Usami, 1998, European Journal of Human Genetics.

Autosomal-dominant, prelingual, nonprogressive sensorineural hearing loss: localization of the gene (DFNA8) to chromosome 11q by linkage in an Austrian family

K. Kirschhofer, F. Wachtler, K. Weipoltshammer, 1998, Cytogenetic and Genome Research.

Genetic heterogeneity of Usher syndrome: analysis of 151 families with Usher type I.

J. Heckenlively, W. Kimberling, M. D. Weston, 2000, American journal of human genetics.