Pages that link to "Q53316213"

The following pages link to Metopic craniosynostosis due to mutations in GLI3: A novel association. (Q53316213):

Displaying 18 items.

• Say-Meyer syndrome: additional manifestations in a new patient and phenotypic assessment (Q30938695) (← links)
• Clinical, genetic and imaging findings identify new causes for corpus callosum development syndromes (Q33654193) (← links)
• Copy-number variations involving the IHH locus are associated with syndactyly and craniosynostosis (Q34458832) (← links)
• Metopic and sagittal synostosis in Greig cephalopolysyndactyly syndrome: five cases with intragenic mutations or complete deletions of GLI3. (Q35083303) (← links)
• Closing the Gap: Genetic and Genomic Continuum from Syndromic to Nonsyndromic Craniosynostoses. (Q35809894) (← links)
• Prevention of premature fusion of calvarial suture in GLI-Kruppel family member 3 (Gli3)-deficient mice by removing one allele of Runt-related transcription factor 2 (Runx2). (Q36033280) (← links)
• Carpenter syndrome: extended RAB23 mutation spectrum and analysis of nonsense-mediated mRNA decay (Q36195863) (← links)
• Hedgehog signaling: networking to nurture a promalignant tumor microenvironment (Q37903167) (← links)
• GLI3-related polydactyly: a review (Q39146281) (← links)
• Loss-of-Function of Gli3 in Mice Causes Abnormal Frontal Bone Morphology and Premature Synostosis of the Interfrontal Suture (Q42036556) (← links)
• A novel GLI3c.750delC truncation mutation in a multiplex Greig cephalopolysyndactyly syndrome family with an unusual phenotypic combination in a patient. (Q43109842) (← links)
• Novel GLI3 variant causing overlapped Greig cephalopolysyndactyly syndrome (GCPS) and Pallister-Hall syndrome (PHS) phenotype with agenesis of gallbladder and pancreas (Q48168747) (← links)
• Regulation of Calvarial Osteogenesis by Concomitant De-repression of GLI3 and Activation of IHH Targets (Q49326948) (← links)
• Genetic advances in craniosynostosis. (Q52795305) (← links)
• Gastric cancer and Hedgehog signaling pathway: emerging new paradigms. (Q54945791) (← links)
• A de novo GLI3 mutation in a patient with acrocallosal syndrome (Q56320109) (← links)
• Signaling Mechanisms Underlying Genetic Pathophysiology of Craniosynostosis (Q61809349) (← links)
• Identification of novel mutations in preaxial polydactyly patients through whole-exome sequencing (Q93146892) (← links)