Department of Cytogenetics |
Designation : Technical officer ‘A’
Education:
S.No. |
Degree |
University |
Subject |
Year |
1 |
M.Sc. |
Mumbai University |
Applied Biology |
2009 |
2. |
DMLT |
Mumbai University |
Haematology,Biochemistry,Microbiology,Clinical Pathology and Histopathology |
October 1986 |
3. |
B.Sc. |
Mumbai University |
Zoology |
May 1984 |
Human Genetics,Mechanism of non-disjunction of chromosome 21; DNA defects and repair in Fanconi anemia.
Publications: 13
International: 6
National: 7
Latest publications:
Vundinti BR, Korgaonkar S, Ghosh K.Incidence of clonal chromosomal abnormalities in Fanconi anemia. Ind J Cancer [In press].
Korgaonkar S , Ghosh K, Jijina F,Vundinti BR. Chromosomal breakage study in children suspected with Fanconi anemia in the Indian population. J Pediatr hematol Oncol 2010;.Nov,32(8):606-10.
Korgaonkar S ,Ghosh K,Vundiniti BR. Clinical genetic and Cytogenetic study of Fanconi anemia in an Indian population. Hematology.2010 Feb;15(1):58-62.
Vundinti BR, Korgaonkar S,Ghosh K. Familial small supernumerary marker chromosome(sSMC) (14) (:p11-q11:) in a child with translocated Down syndrome. Indian J Pediatr.2009 Dec;76(12):1265-7.
Korgaonkar S, Babu VR,Kerketta L,Ghosh K. Chromosomal breakage in myelodysplastic syndrome. Asian Pac J Cancer Prev.2008 Jan-Mar,9(1):151-4.
Rao VB, Kerketta L,Korgaonkar S, Ghosh K. Differention of Nijmegen breakage syndrome from Fanconi anemia. Genet Mol Res.2007 Sep30;(3):622-6.
Babu Rao V, Kerketta L, Korgaonkar S, Ghosh K. Dandy-Walker malformations in a case of partial trisomy 9p(p12.1-pter) due to maternal translocation t(9;12)(p12.1;p13.3). Ind J Hum Genet 2007; 13(1):33-35.
Babu Rao V , Kerketta L, Korgaonkar S, Ghosh K. Pericentric inversion of chromosome 9[inv(9)(p12q13)] : Its association with genetic diseases. Ind J Hum Genet. 2006;12: 129-132.
Rao VB. Kerketta L,Korgaonkar S, Ghosh K, Mohanty D. Maternal origin of extra marker chromosome 1Q31.1-qter and 13pter-q12.12 in a child with dysmorphic features. Genet Cous.2005;16(2):139-43.