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K Prabhakara

Showing results (11-20 of 15) with videos related to

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Annales De Genetique|September 1, 2004
Recurrent proximal 18p monosomy and 18q trisomy in a family with a maternal pericentric inversion of chromosome 18K Prabhakara, Herman E Wyandt, Xin L Huang, et al.
The Indian Journal of Medical Research|October 1, 1996
Improved method for study of chromosomes of chorionic villus samplesM R Chowdhury, R Mathur, K Prabhakara, et al.
Neoplasia (New York, N.Y.)|February 18, 2004
A unique model system for tumor progression in GBM comprising two developed human neuro-epithelial cell lines with differential transforming potential and coexpressing neuronal and glial markersAnjali Shiras, Arti Bhosale, Varsha Shepal, et al.
Indian Journal of Ophthalmology|January 31, 2004
Congenital glaucoma associated with 22p+ variant in a dysmorphic childAnil K Mandal, K Prabhakara, Aramati B M Reddy, et al.
Journal of Medical Genetics|November 1, 2011
Pathogenic aberrations revealed exclusively by single nucleotide polymorphism (SNP) genotyping data in 5000 samples tested by molecular karyotypingD L Bruno, S M White, D Ganesamoorthy, et al.
Pageof 2

Showing results (11-20 of 15) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 15 results.
Annales De Genetique|September 1, 2004
Recurrent proximal 18p monosomy and 18q trisomy in a family with a maternal pericentric inversion of chromosome 18K Prabhakara, Herman E Wyandt, Xin L Huang, et al.
The Indian Journal of Medical Research|October 1, 1996
Improved method for study of chromosomes of chorionic villus samplesM R Chowdhury, R Mathur, K Prabhakara, et al.
Neoplasia (New York, N.Y.)|February 18, 2004
A unique model system for tumor progression in GBM comprising two developed human neuro-epithelial cell lines with differential transforming potential and coexpressing neuronal and glial markersAnjali Shiras, Arti Bhosale, Varsha Shepal, et al.
Indian Journal of Ophthalmology|January 31, 2004
Congenital glaucoma associated with 22p+ variant in a dysmorphic childAnil K Mandal, K Prabhakara, Aramati B M Reddy, et al.
Journal of Medical Genetics|November 1, 2011
Pathogenic aberrations revealed exclusively by single nucleotide polymorphism (SNP) genotyping data in 5000 samples tested by molecular karyotypingD L Bruno, S M White, D Ganesamoorthy, et al.
Pageof 2