Navaratnam Elanko
St George's Hospital(GB)
Publications by Year
Research Areas
Craniofacial Disorders and Treatments, Wnt/β-catenin signaling in development and cancer, Bone Tumor Diagnosis and Treatments, Cleft Lip and Palate Research, dental development and anomalies
Most-Cited Works
- → Functional haploinsufficiency of the human homeobox gene MSX2 causes defects in skull ossification(2000)318 cited
- → Recessive Robinow syndrome, allelic to dominant brachydactyly type B, is caused by mutation of ROR2(2000)303 cited
- → Genomic Screening of Fibroblast Growth-Factor Receptor 2 Reveals a Wide Spectrum of Mutations in Patients with Syndromic Craniosynostosis(2002)265 cited
- → A survey ofTWIST for mutations in craniosynostosis reveals a variable length polyglycine tract in asymptomatic individuals(2001)42 cited
- Autosomal recessive Robinow syndrome is allelic to dominant brachydactyly type B and caused by loss of function mutations in ROR2(2000)
- A survey of TWIST for mutations in craniosynostosis reveals a variable length polyglycine tract in asymptomatic individuals.(2001)
- Autosomal recessive Robinow syndrome is caused by homozygous mutations in ROR2.(2000)
- Mutations of the homeobox gene MSX2 cause symmetric parietal foramina: contrasting effects of loss and gain of function mutations for skull development.(1999)
- → Mutation Analysis of <i>PTPN11</i> in Noonan Syndrome by WAVE(2006)1 cited
- Mutation in the IgII domain of FGFR2 causes the eponymous form of Pfeiffer syndrome.(2001)