Zobrazeno 1 - 10
of 30
pro vyhledávání: '"T S, Sundareshan"'
Autor:
Angel Beula P. Royal, Syeda Sabiha S. Lubna, P Beaulah Angel, Vijaya V Mysorekar, T S Sundareshan
Publikováno v:
Acta Medica International, Vol 5, Iss 2, Pp 74-78 (2018)
Aims: The aim of this study was to evaluate the complexity of the chromosomal abnormalities in multiple myeloma (MM) cases and to correlate the findings with the previous reported cases. Materials and Methods: Bone marrow samples were obtained from p
Externí odkaz:
https://doaj.org/article/4d799a1f433d49a592e077e994b104e5
Publikováno v:
Indian Journal of Pathology and Microbiology, Vol 60, Iss 2, Pp 301-303 (2017)
Externí odkaz:
https://doaj.org/article/17ca79f7b4694eb0b5711548f8879a6d
Publikováno v:
Indian Journal of Pathology and Microbiology, Vol 60, Iss 2, Pp 301-303 (2017)
Autor:
Shah, Aditi *, KS, Nataraj, T S, Sundareshan *, Prabhu, Shilpa *, RAM S, Bharath *, Dalal, Hamza Yusuf *, Komaravelli, Shiva Kumar *, Damodar, Sharat
Publikováno v:
In Blood 5 November 2020 136 Supplement 1:45-46
Publikováno v:
The Indian Journal of Pediatrics. 57:257-260
A child with fragile secondary constriction 2q11 associated with unusual clinical features and psychomotor retardation is described. The pathogenetic significance of this fragile site still remains unclear, and heterogeneity of clinical manifestation
Publikováno v:
Cancer genetics and cytogenetics. 140(1)
The expression of bleomycin-induced fragile sites (FS) in the blood lymphocytes of 150 individuals (100 oral cancer patients and 50 age and sex matched controls) is described. FS expression frequencies in oral cancer patients were significantly highe
Publikováno v:
Cancer genetics and cytogenetics. 134(2)
We report cytogenetic findings from fine-needle aspiration samples of two synovial sarcoma patients. The cases are of interest because (1) one case is of a rare site (submandibular region) of the head and neck, and (2) the other is a patient with syn
Autor:
A M, Udayakumar, T S, Sundareshan, T M, Goud, M G, Devi, S, Biswas, L, Appaji, B S, Arunakumari, K R, Rajan, P S, Prabhakaran
Publikováno v:
Cancer genetics and cytogenetics. 127(1)
Chromosomal analysis was performed in fine needle aspiration samples of 98 primary Ewing tumors (ETs) prior to treatment. Among the 58 (59.18%) successful cultures, t(11;22)(q24;q12) was observed in 87.9% and 6.8% had abnormalities other than t(11;22
Publikováno v:
Indian journal of experimental biology. 28(6)
The frequency and types of acrocentric chromosome association were quantitatively analysed in a Down syndrome child with unusual karyotype, 46, XX, -14, -22, t dic (14p;22p), +21, 21S+. Father and 4 sibs were heterozygous carriers for t dic (14p;22p)
Publikováno v:
American journal of medical genetics. 36(1)
We report on apparently nonmosaic trisomy 22 in a liveborn girl with multiple congenital anomalies. The abnormalities were growth retardation; microcephaly; hypertelorism; epicanthic folds; anti-mongoloid slant; apparently low-set, malformed ears; hi