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Annales De Genetique|January 1, 1985
Complex chromosomal rearrangement involving chromosomes 11, 13, 14 and 18 resulting in monosomy for 13q32----qterS A Al-Awadi, A S Teebi, T S SundareshanAnnales De Genetique|April 6, 2002
Rhabdomyosarcoma: cytogenetics of five cases using fine-needle aspiration samples and review of the literatureA M Udayakumar, T S Sundareshan, L Appaji, et al.Cancer Genetics and Cytogenetics|November 1, 1992
Variant complex translocation t(8;15;21) in acute myeloblastic leukemia (M2) associated with bilateral chloromaT S Sundareshan, M Augustus, T C Yasha, et al.Indian Journal of Pediatrics|March 1, 1990
Familial fragile secondary constriction on chromosome 2 (2q11) with unusual features and psychomotor retardationD S Murthy, A S Teebi, T S Sundareshan, et al.American Journal of Medical Genetics|May 1, 1990
Apparently nonmosaic trisomy 22: clinical report and reviewT S Sundareshan, K K Naguib, S A al-Awadi, et al.Annales De Genetique|January 1, 1986
Klinefelter's syndrome, mosaic 46,XX/46,XY/47,XXY/48,XXXY/48,XXYY: a case reportS A Al-Awadi, A S Teebi, D S Krishna Murthy, et al.Cancer Genetics and Cytogenetics|May 30, 2002
Submandibular synovial sarcoma with t(X;18) and synovial sarcoma of the toe with additional cytogenetic abnormalities: presentation of two cases and review of the literatureA M Udayakumar, T S Sundareshan, G Mukherjee, et al.Indian Journal of Experimental Biology|June 1, 1990
Segregation of acrocentric chromosome association in familial dicentric Robertsonian translocation t(14p;22p), aneuploidy (trisomy-21) and heteromorphismD S Murthy, T S Sundareshan, T I Farag, et al.American Journal of Medical Genetics|August 1, 1989
A new autosomal recessive disorder resembling Weaver syndromeA S Teebi, T S Sundareshan, M Y Hammouri, et al.Journal of Medical Genetics|December 1, 1983
Interstitial deletion of the long arm of chromosome 2: del(2)(q31q33)S A Al-Awadi, T I Farag, K Naguib, et al.Pageof 4