Amanote Research
Register
Sign In
Discover open access scientific publications
Search, annotate, share and cite publications
Publications by Tom Walsh
Five Novel Loci for Inherited Hearing Loss Mapped by SNP-based Homozygosity Profiles in Palestinian Families
European Journal of Human Genetics
Genetics
Profound, Prelingual Nonsyndromic Deafness Maps to Chromosome 10q21 and Is Caused by a Novel Missense Mutation in the Usher Syndrome Type IF Gene PCDH15
European Journal of Human Genetics
Genetics
‹
1
2
Related publications
Novel Recessive PDZD7 Biallelic Mutations in Two Chinese Families With Non-Syndromic Hearing Loss
American Journal of Medical Genetics, Part A
Genetics
Strategies for Developing Novel Therapeutics for Sensorineural Hearing Loss
Frontiers in Pharmacology
Pharmacology
Identification of CDH23 Mutations in Korean Families With Hearing Loss by Whole-Exome Sequencing
BMC Medical Genetics
Genetics
An SNP-Based Linkage Map for Zebrafish Reveals Sex Determination Loci
G3: Genes, Genomes, Genetics
Medicine
Genetics
Molecular Biology
Genome-Wide Screening for Genetic Loci Associated With Noise-Induced Hearing Loss
Mammalian Genome
Genetics
Novel PTPRQ Mutations Identified in Three Congenital Hearing Loss Patients With Various Types of Hearing Loss
Annals of Otology, Rhinology and Laryngology
Medicine
Otorhinolaryngology
Families of Children With Hearing Loss and Parental Educational Practices
Genome-Wide Association Study in Mexican Holstein Cattle Reveals Novel Quantitative Trait Loci Regions and Confirms Mapped Loci for Resistance to Bovine Tuberculosis
Animals
Animal Science
Zoology
Veterinary
A Set of Novel SNP Loci for Differentiating Continental Populations and Three Chinese Populations
PeerJ
Genetics
Molecular Biology
Biochemistry
Biological Sciences
Medicine
Agricultural
Neuroscience
