Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Search Results
8 results
Filters applied: . Clear all
Results are displayed in a computed author sort order.
The Results By Year timeline is not available.
Page 1
Analysis of the WISP3 gene in Indian families with progressive pseudorheumatoid dysplasia.
Am J Med Genet A. 2012 Nov;158A(11):2820-8. doi: 10.1002/ajmg.a.35620. Epub 2012 Sep 17.
Am J Med Genet A. 2012.
PMID: 22987568
GALNS mutations in Indian patients with mucopolysaccharidosis IVA.
Bidchol AM, Dalal A, Shah H, S S, Nampoothiri S, Kabra M, Gupta N, Danda S, Gowrishankar K, Phadke SR, Kapoor S, Kamate M, Verma IC, Puri RD, Sankar VH, Devi AR, Patil SJ, Ranganath P, Jain SJ, Agarwal M, Singh A, Mishra P, Tamhankar PM, Gopinath PM, Nagarajaram HA, Satyamoorthy K, Girisha KM.
Bidchol AM, et al.
Am J Med Genet A. 2014 Nov;164A(11):2793-801. doi: 10.1002/ajmg.a.36735. Epub 2014 Sep 22.
Am J Med Genet A. 2014.
PMID: 25252036
Item in Clipboard
Recurrent and novel GLB1 mutations in India.
Bidchol AM, Dalal A, Trivedi R, Shukla A, Nampoothiri S, Sankar VH, Danda S, Gupta N, Kabra M, Hebbar SA, Bhat RY, Matta D, Ekbote AV, Puri RD, Phadke SR, Gowrishankar K, Aggarwal S, Ranganath P, Sharda S, Kamate M, Datar CA, Bhat K, Kamath N, Shah H, Krishna S, Gopinath PM, Verma IC, Nagarajaram HA, Satyamoorthy K, Girisha KM.
Bidchol AM, et al.
Gene. 2015 Aug 10;567(2):173-81. doi: 10.1016/j.gene.2015.04.078. Epub 2015 Apr 30.
Gene. 2015.
PMID: 25936995
Item in Clipboard
A novel mutation (g.106737G>T) in zone of polarizing activity regulatory sequence (ZRS) causes variable limb phenotypes in Werner mesomelia.
Girisha KM, Bidchol AM, Kamath PS, Shah KH, Mortier GR, Mundlos S, Shah H.
Girisha KM, et al. Among authors: bidchol am.
Am J Med Genet A. 2014 Apr;164A(4):898-906. doi: 10.1002/ajmg.a.36367. Epub 2014 Jan 29.
Am J Med Genet A. 2014.
PMID: 24478176
Item in Clipboard
Phenotype and genotype in patients with Larsen syndrome: clinical homogeneity and allelic heterogeneity in seven patients.
Girisha KM, Bidchol AM, Graul-Neumann L, Gupta A, Hehr U, Lessel D, Nader S, Shah H, Wickert J, Kutsche K.
Girisha KM, et al. Among authors: bidchol am.
BMC Med Genet. 2016 Apr 6;17:27. doi: 10.1186/s12881-016-0290-6.
BMC Med Genet. 2016.
PMID: 27048506
Free PMC article.
Item in Clipboard
White matter changes in GM1 gangliosidosis.
Tuteja M, Bidchol AM, Girisha KM, Phadke S.
Tuteja M, et al. Among authors: bidchol am.
Indian Pediatr. 2015 Feb;52(2):155-6. doi: 10.1007/s13312-015-0593-2.
Indian Pediatr. 2015.
PMID: 25691190
Free article.
Item in Clipboard
Novel mutation in an Indian patient with Methylmalonic Acidemia, cblA type.
Girisha KM, Shrikiran A, Bidchol AM, Sakamoto O, Gopinath PM, Satyamoorthy K.
Girisha KM, et al. Among authors: bidchol am.
Indian J Hum Genet. 2012 Sep;18(3):346-8. doi: 10.4103/0971-6866.108025.
Indian J Hum Genet. 2012.
PMID: 23716945
Free PMC article.
Item in Clipboard
A novel frameshift mutation in TWIST2 gene causing Setleis syndrome.
Girisha KM, Bidchol AM, Sarpangala MK, Satyamoorthy K.
Girisha KM, et al. Among authors: bidchol am.
Indian J Pediatr. 2014 Mar;81(3):302-4. doi: 10.1007/s12098-013-1253-y. Epub 2013 Oct 15.
Indian J Pediatr. 2014.
PMID: 24127007
Item in Clipboard
Cite
Cite