نتائج البحث - "Sundareshan, T S"

1

Prevalence of Genetic Abnormalities in Patients with Multiple Myeloma and Its Clinical Relevance in a Developing Country like India

المؤلفون: Aditi Shah, Sundareshan T S, K.S. Nataraj, Bharath Ram S, Shilpa Prabhu, Sharat Damodar, Hamza Yusuf Dalal, Shiva Kumar Komaravelli

المصدر: Blood. 136:45-46

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::3e508b550936a5561cf7e41eeadb6ef7
https://doi.org/10.1182/blood-2020-141895

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2

Comparison of Diagnostic Yield of a FISH Panel Against Conventional Cytogenetic Studies for Hematological Malignancies: A South Indian Referral Laboratory Analysis Of 201 Cases

المؤلفون: Vishal, Ashok, Ramya, Ranganathan, Smitha, Chander, Sharat, Damodar, Sunil, Bhat, Nataraj K, S, Satish Kumar, A, Sachin Suresh, Jadav, Mahesh, Rajashekaraiah, Sundareshan, T S

المصدر: Asian Pacific Journal of Cancer Prevention : APJCP

مصطلحات موضوعية: Chromosome Aberrations, fungi, India, Prognosis, Chromosomal aberration, cytogenetics, Asian People, Hematologic Neoplasms, Karyotyping, Cytogenetic Analysis, Humans, hematological malignancies, Referral and Consultation, fluorescence in situ hybridization, In Situ Hybridization, Fluorescence, Research Article

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::e7685c5827317cf4f905ab6ba111abfc
https://pubmed.ncbi.nlm.nih.gov/29286619

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3

Academic Journal

Down syndrome in Kuwait

المؤلفون: Al-Awadi, S. A., Farag, T. I., Teebi, A. S., Naguib, K. K., Sundareshan, T. S., Murthy, D. S. Krishna

المصدر: American Journal of Medical Genetics ; volume 37, issue S7, page 87-88 ; ISSN 0148-7299 1096-8628

الاتاحة: http://dx.doi.org/10.1002/ajmg.1320370717
https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fajmg.1320370717
https://onlinelibrary.wiley.com/doi/full/10.1002/ajmg.1320370717

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4

Academic Journal

Unilateral true hermaphrodite with 46,XX/46,XY dispermic chimerism.

المؤلفون: Farag, T I, Al-Awadi, S A, Tippett, P, el-Sayed, M, Sundareshan, T S, Al-Othman, S A, el-Badramany, M H

مصطلحات موضوعية: Research Article

وصف الملف: text/html

Relation: http://jmg.bmj.com/cgi/content/short/24/12/784; http://dx.doi.org/10.1136/jmg.24.12.784

الاتاحة: http://jmg.bmj.com/cgi/content/short/24/12/784
https://doi.org/10.1136/jmg.24.12.784

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5

Academic Journal

Complex translocation involving chromosomes Y, 1, and 3 resulting in deletion of segment 3q23 --- q25.

المؤلفون: Al-Awadi, S A, Naguib, K K, Farag, T I, Teebi, A S, Cuschieri, A, Al-Othman, S A, Sundareshan, T S

مصطلحات موضوعية: Research Article

وصف الملف: text/html

Relation: http://jmg.bmj.com/cgi/content/short/23/1/91; http://dx.doi.org/10.1136/jmg.23.1.91

الاتاحة: http://jmg.bmj.com/cgi/content/short/23/1/91
https://doi.org/10.1136/jmg.23.1.91

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6

Academic Journal

Interstitial deletion of the long arm of chromosome 2: del(2)(q31q33).

المؤلفون: Al-Awadi, S A, Farag, T I, Naguib, K, Teebi, A, Cuschieri, A, Al-Othman, S, Sundareshan, T S

مصطلحات موضوعية: Research Article

وصف الملف: text/html

Relation: http://jmg.bmj.com/cgi/content/short/20/6/464; http://dx.doi.org/10.1136/jmg.20.6.464

الاتاحة: http://jmg.bmj.com/cgi/content/short/20/6/464
https://doi.org/10.1136/jmg.20.6.464

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7

Academic Journal

De novo partial monosomy 21 with unusual karyotype

المؤلفون: Al-Awadi, S. A., Naguib, K. K., Teebi, A. S., Sundareshan, T. S.

المصدر: Japanese Journal of Human Genetics ; volume 31, issue 1, page 45-48 ; ISSN 0021-5074

الاتاحة: http://dx.doi.org/10.1007/bf01876801
http://www.nature.com/articles/jhg19866.pdf
http://www.nature.com/articles/jhg19866
http://www.springerlink.com/index/pdf/10.1007/BF01876801

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8

Academic Journal

Clinical and cytogenetic studies in familial polycystic ovarian disease

المؤلفون: Krishnamurthy, D. S., Naguib, K. K., Al-awadi, S. A., Sundareshan, T. S., Al-othman, S. A., Hayat, A. A., Moustafa, A. N., Diab, M. R.

المصدر: Journal of Obstetrics and Gynaecology ; volume 10, issue 2, page 133-139 ; ISSN 0144-3615 1364-6893

الاتاحة: http://dx.doi.org/10.3109/01443618909151135
http://www.tandfonline.com/doi/pdf/10.3109/01443618909151135

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9

Academic Journal

Apparently nonmosaic trisomy 22: Clinical report and review

المؤلفون: Sundareshan, T. S., Naguib, K. K., Al‐Awadi, S. A., Redha, M. A., Hamoud, M. S.

المصدر: American Journal of Medical Genetics ; volume 36, issue 1, page 7-10 ; ISSN 0148-7299 1096-8628

الاتاحة: http://dx.doi.org/10.1002/ajmg.1320360103
https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fajmg.1320360103
https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.1320360103

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10

Academic Journal

Familial fragile secondary constriction on chromosome 2 (2q11) with unusual features and psychomotor retardation

المؤلفون: Krishna Murthy, D. S., Teebi, A. S., Sundareshan, T. S., Al-Awadi, S. A.

المصدر: The Indian Journal of Pediatrics ; volume 57, issue 2, page 257-260 ; ISSN 0019-5456 0973-7693

الاتاحة: http://dx.doi.org/10.1007/bf02722098
http://link.springer.com/content/pdf/10.1007/BF02722098.pdf
http://link.springer.com/article/10.1007/BF02722098/fulltext.html
http://link.springer.com/content/pdf/10.1007/BF02722098

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11

Academic Journal

5q deletion myelodysplastic syndrome.

المؤلفون: Chari, Preethi S., Chander, Smitha, Sundareshan, T. S., Prasad, Sujay

المصدر: Indian Journal of Pathology & Microbiology; Apr-Jun2017, Vol. 60 Issue 2, p301-303, 3p

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12

Academic Journal

Trisomy 4q: 46, xy,-11, +der (11), t(4;11) (q27; q25) pat in a child with multiple congenital anomalies.

المؤلفون: Al-Awadi, S., Naguib, E., Al-Othman, S., Sundareshan, T., al-Awadi, S A, Naguib, K K, al-Othman, S A, Sundareshan, T S

المصدر: Indian Journal of Pediatrics; Mar1988, Vol. 55 Issue 2, p308-311, 4p

13

Periodical

Cytogenetics of Neuroblastoma : A Study Using Fine Needle Aspiration Cultures

المؤلفون: Udayakumar, A. M., Sundareshan, T. S., Goud, T. Mallana, Biswas, S., Devi, M. Gayathri, Kumari, B. S. Aruna, Appaji, L.

المصدر: Annales de Génétique; 2001, Vol. 44 Issue: 3 p161-166, 6p

14

Periodical

Cytogenetic characterization of Ewing tumors using fine needle aspiration samples

المؤلفون: Udayakumar, A. M., Sundareshan, T. S., Goud, T. M., Devi, M. G., Biswas, S., Appaji, L., Arunakumari, B. S., Rajan, K. R., Prabhakaran, P. S.

المصدر: Cancer Genetics and Cytogenetics; 2001, Vol. 127 Issue: 1 p42-48, 7p

15

Academic Journal

Turner syndrome variants: A report of four cases with review of literature.

المؤلفون: Mysorekar, Vijaya V., Sundareshan, T. S., Kumar, K. M. Prasanna, Raghupathy, P.

المصدر: Perinatology: Journal of Perinatal & Neonatal Care; Jul-Oct2008, Vol. 10 Issue 4/5, p146-148, 3p, 2 Color Photographs

16

Periodical

Expression of Common Fragile Sites in Lymphocytes of Wilms Tumor in Patients, Their Parents, and Siblings

المؤلفون: Sundareshan, T. S., Augustus, M.

المصدر: Cancer Genetics and Cytogenetics; 1995, Vol. 84 Issue: 1 p51-55, 5p

17

Periodical

Cytogenetics of Non-Small Cell Lung Cancer: Simple Technique for Obtaining High Quality Chromosomes by Fine Needle Aspirate Cultures

المؤلفون: Sundareshan, T. S., Augustus, M.

المصدر: Cancer Genetics and Cytogenetics; 1996, Vol. 91 Issue: 1 p53-60, 8p

18

Periodical

De novo partial monosomy 21 with unusual karyotype

المؤلفون: Al-Awadi, S A, Naguib, K K, Teebi, A S, Sundareshan, T S

المصدر: Journal of Human Genetics; March 1986, Vol. 31 Issue: 1 p45-48, 4p

19

Academic Journal

Down syndrome and trisomy 18 in the bedouins

المؤلفون: Farag, T. I., Al‐Awadi, S. A., Al‐Othman, S. A., Sundareshan, T. S., Krishna Murthy, D. S., Usha, R., Mady, S. A., Uma, R., Reynolds, James F.

المصدر: American Journal of Medical Genetics ; volume 29, issue 4, page 943-944 ; ISSN 0148-7299 1096-8628

الاتاحة: http://dx.doi.org/10.1002/ajmg.1320290427
https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fajmg.1320290427
https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.1320290427

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20

Academic Journal

Metacarpophalangeal pattern profile analysis in partial 9pMonosomy

المؤلفون: Al‐Awadi, Sadika A., Farag, Talaat I., Satyanath, Siram, Sundareshan, T. S., Optiz, John M., Reynolds, James F.

المصدر: American Journal of Medical Genetics ; volume 29, issue 1, page 217-219 ; ISSN 0148-7299 1096-8628

الاتاحة: http://dx.doi.org/10.1002/ajmg.1320290128
https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fajmg.1320290128
https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.1320290128

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