T.S. Sundareshan - Concepedia

Author

T.S. Sundareshan

Kuwait Institute for Medical Specialization

Also Known As

Sundareshan T S, T S Sundareshan, T Sundareshan, T. S. Sundareshan, T.S Sundareshan, T.S. Sundareshan, TS Sundareshan

Publications

389

Citations

H-Index

Concepts

All Affiliations

Kuwait Institute for Medical Specialization Kidwai Memorial Institute of Oncology

About

T.S. Sundareshan is an author at Kuwait Institute for Medical Specialization specializing in pathology, medicine, and cytogenetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	4	4	64
2	Health Sciences	1	1	15
3	Public Health	1	1	15
4	Cell Biology	1	1	28
5	Molecular Genetics	1	1	28

T.S. Sundareshan

Publications

188

Citations

H-Index

Page 1

	Year	Citations
Complex translocation involving chromosomes Y, 1, and 3 resulting in deletion of segment 3q23----q25. S A Al-Awadi, Kamal K. Naguib, Talaat I. Farag, Journal of Medical Genetics	1986	38
Interstitial deletion of the long arm of chromosome 2: del(2)(q31q33). S A Al-Awadi, Talaat I. Farag, Kamal K. Naguib, Journal of Medical Genetics Gene Deletion DataCytogeneticsGeneticsPathologyClinical Features	1983	28
Direct duplication of chromosome 1, dir dup(1)(p21.2 → p32) in a Bedouin boy with multiple congenital anomalies F. Mohammed, Talaat I. Farag, S. S. Gunawardana, American Journal of Medical Genetics	1989	23
Down syndrome in Kuwait Sadiqa Al-Awadi, Talaat I. Farag, A. S. Teebi, American Journal of Medical Genetics	2005	19
A new autosomal recessive disorder resembling Weaver syndrome Ahmad S. Teebi, T.S. Sundareshan, Mousa Y. Hammouri, American Journal of Medical Genetics	1989	18
Unilateral true hermaphrodite with 46,XX/46,XY dispermic chimerism. Talaat I. Farag, S A Al-Awadi, Patricia Tippett, Journal of Medical Genetics Year Old FemaleAmbiguous External GenitaliaInfertilityAndrologyFertility	1987	15
Variant complex translocation t(8;15;21) in acute myeloblastic leukemia (M2) associated with bilateral chloroma T.S. Sundareshan, Meena Augustus, T.C. Yasha, Cancer Genetics and Cytogenetics Hematological MalignancyAcute Myeloblastic LeukemiaMixed-phenotype Acute LeukemiaHematologyMyeloid Neoplasia	1992	15
De novo partial monosomy 21 with unusual karyotype S A Al-Awadi, Kamal K. Naguib, A. S. Teebi, The Japanese Journal of Human Genetics Karyotype ImagingUnusual KaryotypeCytogeneticsGenetic DisorderGenetics	1986	11
Klinefelter's syndrome, mosaic 46,XX/46,XY/47,XXY/48,XXXY/48,XXYY: a case report. S A Al-Awadi, A. S. Teebi, D. S. Krishna Murthy, PubMed	1986	11
Tetrasomy 21 as a sole abnormality in erythroleukemia A.M. Udayakumar, T.S. Sundareshan Cancer Genetics and Cytogenetics Hematological MalignancyHematologyHistopathologyPathologySole Abnormality	1995	10

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