Prabhakara K - Search Results

1

Extending the scope of diagnostic chromosome analysis: detection of single gene defects using high-resolution SNP microarrays.

Bruno DL, Stark Z, Amor DJ, Burgess T, Butler K, Corrie S, Francis D, Ganesamoorthy D, Hills L, James PA, O'Rielly D, Oertel R, Savarirayan R, Prabhakara K, Salce N, Slater HR. Bruno DL, et al. Among authors: prabhakara k. Hum Mutat. 2011 Dec;32(12):1500-6. doi: 10.1002/humu.21581. Epub 2011 Sep 19. Hum Mutat. 2011. PMID: 21850686

2

Pathogenic aberrations revealed exclusively by single nucleotide polymorphism (SNP) genotyping data in 5000 samples tested by molecular karyotyping.

Bruno DL, White SM, Ganesamoorthy D, Burgess T, Butler K, Corrie S, Francis D, Hills L, Prabhakara K, Ngo C, Norris F, Oertel R, Pertile MD, Stark Z, Amor DJ, Slater HR. Bruno DL, et al. Among authors: prabhakara k. J Med Genet. 2011 Dec;48(12):831-9. doi: 10.1136/jmedgenet-2011-100372. Epub 2011 Oct 29. J Med Genet. 2011. PMID: 22039585

3

Prenatal detection of deletion-duplication of chromosome 3 arising from meiotic recombination of a familial pericentric inversion.

Prabhakara K, Bruno DL, Padman P, Prasad S, Sudheer Kumar R, Slater HR, Radha Ramadevi A. Prabhakara K, et al. Prenat Diagn. 2008 May;28(5):466-8. doi: 10.1002/pd.2005. Prenat Diagn. 2008. PMID: 18438967 No abstract available.

4

Premature centromere division versus C-anaphases in cultures: need for consensus and guidelines.

Prabhakara K, Radha Ramadevi A. Prabhakara K, et al. Am J Med Genet A. 2004 Jan 30;124A(3):331; author reply 332. doi: 10.1002/ajmg.a.20310. Am J Med Genet A. 2004. PMID: 14708111 No abstract available.

5

Association of parental hyperhomocysteinemia and C677T Methylene tetrahydrofolate reductase (MTHFR) polymorphism with recurrent pregnancy loss.

Govindaiah V, Naushad SM, Prabhakara K, Krishna PC, Radha Rama Devi A. Govindaiah V, et al. Among authors: prabhakara k. Clin Biochem. 2009 Mar;42(4-5):380-6. doi: 10.1016/j.clinbiochem.2008.12.003. Epub 2008 Dec 16. Clin Biochem. 2009. PMID: 19111530

6

De novo pericentric inversion of chromosome 4, inv(4)(p16q12) in a boy with piebaldism and mental retardation.

Ramadevi AR, Naik U, Dutta U, Srikanth, Prabhakara K. Ramadevi AR, et al. Among authors: prabhakara k. Am J Med Genet. 2002 Nov 22;113(2):190-2. doi: 10.1002/ajmg.10739. Am J Med Genet. 2002. PMID: 12407711

7

Premature chromosome condensation in a child with trisomy 21.

Prabhakara K, Kar B, Murthy SK. Prabhakara K, et al. J Med Genet. 1992 Oct;29(10):750-1. doi: 10.1136/jmg.29.10.750. J Med Genet. 1992. PMID: 1433241 Free PMC article. No abstract available.

8

Familial (11;21)(p13;q22)pat balanced reciprocal translocation in a female child with regression of milestones.

Ramadevi AR, Prabhakara K, Dutta U. Ramadevi AR, et al. Among authors: prabhakara k. Ann Genet. 2002 Jan-Mar;45(1):13-5. doi: 10.1016/s0003-3995(02)01099-7. Ann Genet. 2002. PMID: 11934384

9

Recurrent proximal 18p monosomy and 18q trisomy in a family with a maternal pericentric inversion of chromosome 18.

Prabhakara K, Wyandt HE, Huang XL, Prasad KS, Ramadevi AR. Prabhakara K, et al. Ann Genet. 2004 Jul-Sep;47(3):297-303. doi: 10.1016/j.anngen.2004.03.007. Ann Genet. 2004. PMID: 15337476

10

Partial 15q22 trisomy due to segregation of maternal 10;15 reciprocal translocation.

Prabhakara K, Dutta U, Ramadevi AR. Prabhakara K, et al. Indian Pediatr. 2002 Nov;39(11):1050-4. Indian Pediatr. 2002. PMID: 12466578 No abstract available.

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