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Clinical Genetics|July 28, 1999
Pure trisomy 10p involving an isochromosome 10pS A Berend, L G Shaffer, B A BejjaniAmerican Journal of Medical Genetics|December 8, 1998
Combined trisomy 9 and Ullrich-Turner syndrome in a girl with a 46,X,der(9)t(X;9)(q12;q32) karyotypeS Canún, O Mutchinick, L G Shaffer, et al.American Journal of Human Genetics|July 1, 1997
Simultaneous, multilocus FISH analysis for detection of microdeletions in the diagnostic evaluation of developmental delay and mental retardationA H Ligon, A L Beaudet, L G ShafferPrenatal Diagnosis|June 9, 1999
Prenatal diagnosis of Charcot-Marie-Tooth disease type 1A by interphase fluorescence in situ hybridizationC D Kashork, J R Lupski, L G ShafferAnticancer Research|August 6, 2000
Amplification and overexpression of HER-2/neu are uncommon in advanced stage melanomaD L Persons, D A Arber, J A Sosman, et al.American Journal of Clinical Pathology|December 1, 1994
Fluorescence in situ hybridization analysis of trisomy 12 in ovarian tumorsD L Persons, L C Hartmann, J F Herath, et al.American Journal of Medical Genetics|May 15, 1994
Multiple congenital anomalies in a man with (X;6) translocationL E Sivak, J Esbenshade, A R Brothman, et al.Cancer Genetics and Cytogenetics|June 1, 1995
Molecular cytogenetic analysis of a t(7;10) in a human glioblastoma cell lineD Fults, C A Pedone, X L Zhu, et al.Cancer Genetics and Cytogenetics|September 15, 1999
A group of previously not recognized cytogenetic abnormalities in myeloid hematological malignanciesZ Chen, K Richkind, S Roherty, et al.Cancer Genetics and Cytogenetics|June 1, 1997
Myelodysplastic syndrome presenting with clonal rearrangement isolated to chromosomal region 1qM J Mogul, K Brady, A R Brothman, et al.Pageof 22