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Hematology (Amsterdam, Netherlands)|February 6, 2010
Clinical, genetic and cytogenetic study of Fanconi anemia in an Indian populationSeema Korgaonkar, Kanjaksha Ghosh, Babu Rao VundintiJournal of Human Reproductive Sciences|July 21, 2011
A first case of primary amenorrhea with i(X)(qter---q10::---qter), rob(13;14)(q10;q10), inv(9)(p13q33) karyotypeSeema Korgaonkar, Kanjaksha Ghosh, Babu Rao VundintiGene|February 21, 2012
De novo origin of multiple small supernumerary marker chromosomes (sSMCs) in a child with intellectual disability and dysmorphic featuresBabu Rao Vundinti, Seema Korgaonkar, Kanjaksha GhoshIndian Journal of Pediatrics|December 17, 2009
Familial small supernumerary marker chromosome (sSMC) (14)(:p11-q11:) [corrected] in a child with translocation Down syndromeBabu Rao Vundinti, Seema Korgaonkar, Kanjaksha GhoshIntractable & Rare Diseases Research|March 19, 2019
Partial trisomy 9 (9pter->9q22.1) and partial monosomy 14 (14pter- >14q11.2) due to paternal translocation t(9;14)(q22.1;q11.2) in a case of Dysmorphic featuresSomprakash Dhangar, Seema Korgaonkar, Babu Rao VundintiAsian Pacific Journal of Cancer Prevention : APJCP|April 29, 2008
Chromosomal breakage in myelodysplatic syndromeSeema Korgaonkar, V Rao Babu, Lily Kerketta, et al.Indian Journal of Human Genetics|September 30, 2011
Dandy-Walker malformations in a case of partial trisomy 9p (p12.1→pter) due to maternal translocation t(9;12)(p12.1;p13.3)Babu Rao Vundinti, Lily Kerketta, Seema Korgaonkar, et al.Indian Dermatology Online Journal|October 20, 2021
A Cross-Sectional Study to Correlate Disease Severity in Bullous Pemphigoid Patients with Serum Levels of Autoantibodies Against BP180 and BP230Naziya Muhammed, Seema Korgaonkar, Vandana Pradhan, et al.Annals of Hematology|October 21, 2015
Association of XPD (Lys751Gln) and XRCC1 (Arg280His) gene polymorphisms in myelodysplastic syndromeDolly Joshi, Seema Korgaonkar, Chandrakala Shanmukhaiah, et al.Journal of Pediatric Hematology/Oncology|October 1, 2010
Chromosomal breakage study in children suspected with Fanconi anemia in the Indian populationSeema Korgaonkar, Kanjaksha Ghosh, Farah Jijina, et al.Pageof 2