Condition: OROFACIODIGITAL SYNDROME VI


rs1321423759 in CPLANE1 gene and OROFACIODIGITAL SYNDROME VI PMID 22425360 2012 Mutations in C5ORF42 cause Joubert syndrome in the French Canadian population.

PMID 25846457 2015 Exome sequencing identifies a homozygous C5orf42 variant in a Turkish kindred with oral-facial-digital syndrome type VI.

PMID 24178751 2014 C5orf42 is the major gene responsible for OFD syndrome type VI.

PMID 27081551 2015 Exome sequencing identifies novel mutations in C5orf42 in patients with Joubert syndrome with oral-facial-digital anomalies.

PMID 27434533 2016 Molecular genetic analysis of 30 families with Joubert syndrome.

PMID 28431631 2017 Neuroimaging findings in Joubert syndrome with C5orf42 gene mutations: A milder form of molar tooth sign and vermian hypoplasia.

PMID 21448235 2011 Clinical utility gene card for: Joubert syndrome.

PMID 24091540 2013 Diagnostic utility of whole exome sequencing in patients showing cerebellar and/or vermis atrophy in childhood.

PMID 26092869 2015 Joubert syndrome: a model for untangling recessive disorders with extreme genetic heterogeneity.

PMID 28289185 2017 Fifteen years of research on oral-facial-digital syndromes: from 1 to 16 causal genes.

PMID 25920555 2016 Joubert syndrome: genotyping a Northern European patient cohort.

PMID 25407461 2015 Oral-facial-digital syndrome type VI: is C5orf42 really the major gene?

PMID 28125082 2017 Molecular genetic findings and clinical correlations in 100 patients with Joubert syndrome and related disorders prospectively evaluated at a single center.