DOCSLIB.ORG
Explore
Sign Up
Log In
Upload
Search
Home
» Tags
» BBS12
BBS12
Indian Journal for the Practicing Doctor Vol 7 Issue 1
“The Impact of ART on Genome‐Wide Oxidation of 5‐Methylcytosine and the Transcriptome During Early Mouse Development”
Whole Exome Sequencing Identifies Causative Mutations in the Majority of Consanguineous Or Familial Cases with Childhood-Onset I
UC San Francisco Previously Published Works
README Version Is Dedicated to the Human Genome
BBS6, BBS10, and BBS12 Form a Complex with CCT/Tric Family Chaperonins and Mediate Bbsome Assembly
Cystic Kidney Diseases and During Vertebrate Gastrulation
Biomédica 2018;38:451-2 Biomédica Revista Del Instituto Nacional De Salud Volumen 38, No
Ciliopathies
Ciliary Genes in Renal Cystic Diseases
Targeted High-Throughput Sequencing for Diagnosis of Genetically Heterogeneous Diseases: Efficient Mutation Detection in Bardet
ARTICLE Identification of a Novel BBS Gene (BBS12)
Next Generation Sequencing Identifies Five Novel Mutations In
Bardet-Biedl Syndrome: a Study of the Renal and Cardiovascular Phenotypes in a French Cohort
Mouse Models of Inherited Retinal Degeneration with Photoreceptor Cell Loss
WO 2014/089124 Al 12 June 20 14 ( 12.06.20 14) W P O P C T
What's New in Genetics
Biedl Syndrome
Top View
BBS10 Gene Bardet-Biedl Syndrome 10
Genetic Testing for Developmental Disabilities, Intellectual Disability, and Autism Spectrum Disorder Technical Brief Number 23
Bardet–Biedl Syndrome: Beyond the Cilium
Genetics and Genomics: Applications to Developmental Disability
The Cyprinodon Variegatus Genome Reveals Gene Expression Changes Underlying Differences in Skull Morphology Among Closely Related Species Ezra S
The Cyprinodon Variegatus Genome Reveals Gene Expression Changes Underlying Differences in Skull Morphology Among Closely Related Species Ezra S
Structure and Activation Mechanism of the Bbsome Membrane-Protein Trafficking Complex Sandeep Singh1, Miao Gui1, Fujiet Koh1,2, Matthew C.J
Mutation Profile of BBS Genes in Patients with Bardet–Biedl Syndrome
Identification of a Novel Compound Heterozygous Mutation in BBS12 in an Iranian Family with Bardet-Biedl Syndrome Using Targeted Next Generation Sequencing
Next-Generation Sequencing in the Diagnosis of Patients with Bardet–Biedl Syndrome—New Variants and Relationship with Hyperglycemia and Insulin Resistance
Genotype-Phenotype Correlations in Bardet-Biedl Syndrome
Direct Evidence for Bbsome-Associated Intraflagellar
Bardet Biedl Syndrome
Platform Abstracts
Developmental Disruptions Underlying Brain Abnormalities in Ciliopathies
Cilia and Obesity
STAT Autism and Intellectual Disability Panel
Integrated Small Copy Number Variations and Epigenome Maps of Disorders of Sex Development