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U Surti

Showing results (71-80 of 89) with videos related to

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Cancer Genetics and Cytogenetics|January 15, 1998
Molecular analysis of chromosome 7q21.3 in uterine leiomyoma: analysis using markers with linkage to insulin resistanceS M Sell, O Altungoz, A A Prowse, et al.
Prenatal Diagnosis|March 1, 1997
The use of interphase FISH for prenatal diagnosis of Pallister-Killian syndromeP A Mowery-Rushton, M P Stadler, S J Kochmar, et al.
Placenta|March 23, 2011
Recurrent triploid and dispermic conceptions in patients with NLRP7 mutationsR Slim, A Ao, U Surti, et al.
Cancer Genetics and Cytogenetics|May 1, 1991
Nonrandom cytogenetic changes in leiomyomas of the female genitourinary tract. A report of 35 casesM Kiechle-Schwarz, C Sreekantaiah, C S Berger, et al.
Genes, Chromosomes & Cancer|July 1, 1997
Two discrete regions of deletion at 7q in uterine leiomyomasC S Ishwad, R E Ferrell, K Hanley, et al.
Human Genetics|May 1, 1987
A hypervariable region at the D19S11 locusN E Buroker, L Bufton, U Surti, et al.
American Journal of Human Genetics|February 1, 1996
Gene structure, DNA methylation, and imprinted expression of the human SNRPN geneC C Glenn, S Saitoh, M T Jong, et al.
American Journal of Medical Genetics|February 15, 1994
Three unrelated cases of paracentric inversions of 1p in individuals with abnormal phenotypesA M Estop, V Bansal, A Lin, et al.
Progress in Clinical and Biological Research|January 1, 1989
Gene-centromere mapping and the study of non-disjunction in autosomal trisomies and ovarian teratomasA Chakravarti, P P Majumder, S A Slaugenhaupt, et al.
American Journal of Medical Genetics. Part A|March 31, 2007
Cryptic duplication of 12q24.33 --> qter in a child with Angelman syndrome-simultaneous occurrence of two unrelated cytogenetic eventsM Sathanoori, J Hu, V Murthy, et al.
Pageof 9

Showing results (71-80 of 89) with videos related to

Sort By:
Pageof 9
Cancer Genetics and Cytogenetics|January 15, 1998
Molecular analysis of chromosome 7q21.3 in uterine leiomyoma: analysis using markers with linkage to insulin resistanceS M Sell, O Altungoz, A A Prowse, et al.
Prenatal Diagnosis|March 1, 1997
The use of interphase FISH for prenatal diagnosis of Pallister-Killian syndromeP A Mowery-Rushton, M P Stadler, S J Kochmar, et al.
Placenta|March 23, 2011
Recurrent triploid and dispermic conceptions in patients with NLRP7 mutationsR Slim, A Ao, U Surti, et al.
Cancer Genetics and Cytogenetics|May 1, 1991
Nonrandom cytogenetic changes in leiomyomas of the female genitourinary tract. A report of 35 casesM Kiechle-Schwarz, C Sreekantaiah, C S Berger, et al.
Genes, Chromosomes & Cancer|July 1, 1997
Two discrete regions of deletion at 7q in uterine leiomyomasC S Ishwad, R E Ferrell, K Hanley, et al.
Human Genetics|May 1, 1987
A hypervariable region at the D19S11 locusN E Buroker, L Bufton, U Surti, et al.
American Journal of Human Genetics|February 1, 1996
Gene structure, DNA methylation, and imprinted expression of the human SNRPN geneC C Glenn, S Saitoh, M T Jong, et al.
American Journal of Medical Genetics|February 15, 1994
Three unrelated cases of paracentric inversions of 1p in individuals with abnormal phenotypesA M Estop, V Bansal, A Lin, et al.
Progress in Clinical and Biological Research|January 1, 1989
Gene-centromere mapping and the study of non-disjunction in autosomal trisomies and ovarian teratomasA Chakravarti, P P Majumder, S A Slaugenhaupt, et al.
American Journal of Medical Genetics. Part A|March 31, 2007
Cryptic duplication of 12q24.33 --> qter in a child with Angelman syndrome-simultaneous occurrence of two unrelated cytogenetic eventsM Sathanoori, J Hu, V Murthy, et al.
Pageof 9