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BSND
Mutations of BSND Can Cause Nonsyndromic Deafness Or Bartter Syndrome
Mclean, Chelsea.Pdf
A Comprehensive Review on Inherited Sensorineural Hearing Loss and Their Syndromes
Molecular Architecture Underlying Fluid Absorption by the Developing Inner
Open Chromatin Dynamics in Prosensory Cells of the Embryonic Mouse Cochlea Received: 10 February 2019 Brent A
Antenatal Bartter's Syndrome with Sensorineural Deafness
A New Autosomal Recessive Nonsyndromic Hearing Impairment Locus DFNB96 on Chromosome 1P36.31–P36.13
Bartter Syndrome
Mimicry and Well Known Genetic Friends: Molecular Diagnosis in An
Gnomad Lof Supplement
A Novel Mutation Associated with Type III Bartter Syndrome: a Report of Five Cases
Clinical and Genetic Spectrum of Bartter Syndrome Type 3
In-Depth Bioinformatic Study of the CLDN16 Gene and Protein: Prediction of Subcellular Localization to Mitochondria
Identification of Missense Mutation (I12T) in the BSND Gene And
Mouse Genetics Reveals Barttin As a Genetic Modifier of Joubert Syndrome
Spectrum of Genetic Variants in Moderate to Severe Sporadic
Identification of Missense Mutation (I12T) in the BSND Gene And
Blood Pressure Regulation Evolved from Basic Homeostatic Components
Top View
Loss-Of-Function DNA Sequence Variant in the CLCNKA Chloride Channel Implicates the Cardio-Renal Axis in Interindividual Heart Failure Risk Variation
Genetic Hearing Loss
Multiple Long Runs of Homozygosity Detected by SNP Array: Offspring of Consanguineous Parents and His Siblings
Exome Sequencing
Molecular Genetic and Phenotypic Analysis of ENU-Induced Mutant Mouse Models for Biomedical Research
Rectal Cancer in a Patient with Bartter Syndrome: a Case Report
Cody Barta-Transcriptome Characterization of Adult Zebrafish
Simultaneous Homozygous Mutations in SLC12A3 and CLCNKB in an Inbred Chinese Pedigree
Simultaneous Mutations in the CLCNKB and SLC12A3 Genes in Two Siblings with Phenotypic Heterogeneity in Classic Bartter Syndrome