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TTC8
Educational Paper Ciliopathies
Monogenic Causation in Chronic Kidney Disease
Diagnostic Test: OBESITÀ GENETICHE MENDELIANE
Renal Cystic Disorders Infosheet 6-14-19
Modeling Ciliopathies: Primary Cilia in Development and Disease
BBS1 Mutations in a Wide Spectrum of Phenotypes Ranging from Nonsyndromic Retinitis Pigmentosa to Bardet-Biedl Syndrome
Evolution of Modular Intraflagellar Transport from a Coatomer-Like
MVL - Institutional & Self-Pay Test Price List *All Prices Are for Institutional Clients and Self-Pay ONLY
Targeted High-Throughput Sequencing for Diagnosis of Genetically Heterogeneous Diseases: Efficient Mutation Detection in Bardet
Ciliopathies: Genetics in Pediatric Medicine
Mouse Models of Inherited Retinal Degeneration with Photoreceptor Cell Loss
What's New in Genetics
Ciliopathies
Ciliopathies: Genetics in Pediatric Medicine
The Bbsome Assembly Is Spatially Controlled by BBS1 and BBS4 in Human Cells
Genetic Testing for Developmental Disabilities, Intellectual Disability, and Autism Spectrum Disorder Technical Brief Number 23
Bardet–Biedl Syndrome: Beyond the Cilium
Kidneyseq™ V4 – 312 Genes CAKUT Branchiooculofacial Syndrome AD
Top View
Kidneyseq™: a Comprehensive Inherited Kidney Disease Panel Iowa Institute of Human Genetics
Genetics and Genomics: Applications to Developmental Disability
Perkinelmer Genomics to Request the Saliva Swab Collection Kit for Patients That Cannot Provide a Blood Sample As Whole Blood Is the Preferred Sample
Nuclear Roles for Cilia-Associated Proteins
Monogenic Obesity Infosheet 6-14-19
The Nonmotile Ciliopathies Jonathan L
A Coding Variant in the Gene Bardet-Biedl Syndrome 4 (BBS4) Is Associated with a Novel Form of Canine Progressive Retinal Atrophy
Rabbit Anti-TTC8/FITC Conjugated Antibody-SL11510R-FITC
Somatic Mutations in Renal Cyst Epithelium in Autosomal Dominant Polycystic Kidney Disease
Ciliary Proteins-Nuclear-Final-Figures
Identification of a Novel Compound Heterozygous Mutation in BBS12 in an Iranian Family with Bardet-Biedl Syndrome Using Targeted Next Generation Sequencing
Glaab, Enrico (2011) Analysing Functional Genomics Data Using
Bardet Biedl Syndrome
381-388 Cshperspect-CIL-Index 381..388
A Novel Compound Heterozygous Mutation in TTC8 Identified in A
EGL Test Description
Kidneyseq™ Iowa Institute of Human Genetics
Developmental Disruptions Underlying Brain Abnormalities in Ciliopathies