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Publications by Valerie Newton

DFNB20: A Novel Locus for Autosomal Recessive, Non-Syndromal Sensorineural Hearing Loss Maps to Chromosome 11q25–qter

European Journal of Human Genetics

English

Related publications

A Third Novel Locus for Primary Autosomal Recessive Microcephaly Maps to Chromosome 9q34

American Journal of Human Genetics

English

Genome-Wide Analysis Reveals a Novel Autosomal-Recessive Hearing Loss Locus DFNB80 on Chromosome 2p16.1-P21

Journal of Human Genetics

English

A New Locus for Autosomal Recessive Hereditary Spastic Paraplegia Maps to Chromosome 16q24.3

American Journal of Human Genetics

English

DFNB39, a Recessive Form of Sensorineural Hearing Impairment, Maps to Chromosome 7q11.22–q21.12

European Journal of Human Genetics

English

A Novel Locus for Autosomal Dominant Nonsyndromic Hearing Loss, DFNA50, Maps to Chromosome 7q32 Between the DFNB17 and DFNB13 Deafness Loci

Journal of Medical Genetics

English

Mutation of COL11A2 Causes Autosomal Recessive Non-Syndromic Hearing Loss at the DFNB53 Locus

Journal of Medical Genetics

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Novel Mutations Confirm That COL11A2 Is Responsible for Autosomal Recessive Non-Syndromic Hearing Loss DFNB53

Molecular Genetics and Genomics

Molecular Biology

English

Mapping of a Novel Autosomal Recessive Nonsyndromic Deafness Locus (DFNB46) to Chromosome 18p11.32-P11.31

American Journal of Medical Genetics, Part A

English

A Gene for Fluctuating, Progressive Autosomal Dominant Nonsyndromic Hearing Loss, DFNA16, Maps to Chromosome 2q23-24.3

American Journal of Human Genetics

English