Amanote Research
Register
Sign In
Discover open access scientific publications
Search, annotate, share and cite publications
Publications by Tracey Cater
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
Related publications
A Novel Missense Mutation p.L76P in the GJB2 Gene Causing Nonsyndromic Recessive Deafness in a Brazilian Family
Brazilian Journal of Medical and Biological Research
Immunology
Cell Biology
Pharmacology
Biochemistry
Biophysics
Neuroscience
Medicine
Toxicology
Physiology
Pharmaceutics
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
Genetics
Mapping of a Novel Autosomal Recessive Nonsyndromic Deafness Locus (DFNB46) to Chromosome 18p11.32-P11.31
American Journal of Medical Genetics, Part A
Genetics
A Novel Missense Mutation in USP26 Gene Is Associated With Nonobstructive Azoospermia
Reproductive Sciences
Gynecology
Obstetrics
Rhizomelic Chondrodysplasia Punctata Type 1 Caused by a Novel Mutation in the PEX7 Gene
JCRPE Journal of Clinical Research in Pediatric Endocrinology
Child Health
Endocrinology
Perinatology
Pediatrics
Metabolism
Diabetes
A Novel Missense Mutation in the Second Extracellular Domain of GJB2, p.Ser183Phe, Causes a Syndrome of Focal Palmoplantar Keratoderma With Deafness
American Journal of Pathology
Forensic Medicine
Pathology
Crisponi Syndrome Is Caused by Mutations in the CRLF1 Gene and Is Allelic to Cold-Induced Sweating Syndrome Type 1
American Journal of Human Genetics
Genetics
Long QT Syndrome With Nocturnal Cardiac Events Caused by a KCNH2 Missense Mutation (G604S)
Internal Medicine
Internal Medicine
Medicine
Mutations of Cx26 Gene (GJB2) for Prelingual Deafness in Taiwan
European Journal of Human Genetics
Genetics
