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Items: 8

1.

Look Up to Diagnose Down!

Francis F, Bhat V, Balachander B, Khare C, Bethou A, Dalal A, Ponnala R.

Indian J Pediatr. 2017 Dec;84(12):961-962. doi: 10.1007/s12098-017-2421-2. Epub 2017 Jul 29. No abstract available.

PMID:
28755174
2.
3.

Chromosomal abnormalities in amenorrhea: a retrospective study and review of 637 patients in South India.

Dutta UR, Ponnala R, Pidugu VK, Dalal AB.

Arch Iran Med. 2013 May;16(5):267-70. doi: 013165/AIM.005.

4.

An integrated genome-wide approach to discover tumor-specific antigens as potential immunologic and clinical targets in cancer.

Xu QW, Zhao W, Wang Y, Sartor MA, Han DM, Deng J, Ponnala R, Yang JY, Zhang QY, Liao GQ, Qu YM, Li L, Liu FF, Zhao HM, Yin YH, Chen WF, Zhang Y, Wang XS.

Cancer Res. 2012 Dec 15;72(24):6351-61. doi: 10.1158/0008-5472.CAN-12-1656. Epub 2012 Nov 7.

5.

Phenotypic and molecular characterization of partial trisomy 2q resulting from insertion-duplication in chromosome 18q: a case report and review of literature.

Ponnala R, Ranganath P, Dutta UR, Pidugu VK, Dalal AB.

Cytogenet Genome Res. 2012;136(3):229-34. doi: 10.1159/000336974. Epub 2012 Mar 7. Review.

PMID:
22398442
6.

Mosaic trisomy 9 presenting with congenital heart disease, facial dysmorphism and pigmentary skin lesions: intricate issues of genetic counseling.

Patil SJ, Ponnala R, Shah S, Dalal A.

Indian J Pediatr. 2012 Jun;79(6):806-9. doi: 10.1007/s12098-011-0567-x.

PMID:
21975655
7.

Partial monosomy 7q.

Ponnala R, Dalal A.

Indian Pediatr. 2011 May;48(5):399-401.

PMID:
21654006
8.

An integrative approach to reveal driver gene fusions from paired-end sequencing data in cancer.

Wang XS, Prensner JR, Chen G, Cao Q, Han B, Dhanasekaran SM, Ponnala R, Cao X, Varambally S, Thomas DG, Giordano TJ, Beer DG, Palanisamy N, Sartor MA, Omenn GS, Chinnaiyan AM.

Nat Biotechnol. 2009 Nov;27(11):1005-11. doi: 10.1038/nbt.1584. Epub 2009 Nov 1.

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