Kalidas K

Kalidas K

Bengaluru Central University - Taxila / India
Business & Management / Business Administration
AD Scientific Index ID: 4660515
बेंगलुरु सेंट्रल यूनिवर्सिटी
person_outline Kalidas K's MOST POPULAR ARTICLES
1-) Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome M Tartaglia, EL Mehler, R Goldberg, G Zampino, HG Brunner, H Kremer, ... Nature genetics 29 (4), 465-468, 2001 17802001
2-) PTPN11 mutations in Noonan syndrome: molecular spectrum, genotype-phenotype correlation, and phenotypic heterogeneityM Tartaglia, K Kalidas, A Shaw, X Song, DL Musat, I van der Burgt, ...The American Journal of Human Genetics 70 (6), 1555-1563, 20028632002
3-) A gene encoding a transmembrane protein is mutated in patients with diabetes mellitus and optic atrophy (Wolfram syndrome)H Inoue, Y Tanizawa, J Wasson, P Behn, K Kalidas, E Bernal-Mizrachi, ...Nature genetics 20 (2), 143-148, 19988591998
4-) The natural history of Noonan syndrome: a long-term follow-up studyAC Shaw, K Kalidas, AH Crosby, S Jeffery, MA PattonArchives of disease in childhood 92 (2), 128-132, 20073192007
5-) Mutation in vascular endothelial growth factor-C, a ligand for vascular endothelial growth factor receptor-3, is associated with autosomal dominant milroy-like primary lymphedemaK Gordon, D Schulte, G Brice, MA Simpson, MG Roukens, A Van Impel, ...Circulation research 112 (6), 956-960, 20131942013