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Cytogenetic and Genome Research|April 18, 2009
10p11.2 to 10q11.2 is a yet unreported region leading to unbalanced chromosomal abnormalities without phenotypic consequencesT Liehr, M Stumm, R D Wegner, et al.Acta Haematologica|February 1, 2013
An unusual cytogenetic rearrangement originating from two different abnormalities in chromosome 6 in a child with acute promyelocytic leukemiaR R C Matos, H Mkrtchyan, B A S Amaral, et al.Genetics and Molecular Research : GMR|May 8, 2010
Identification of a de novo inv dup(X)(pter--> q22) by multicolor banding in a girl with Turner syndromeP Burégio-Frota, L Valença, G F Leal, et al.Molecular Medicine Reports|April 8, 2011
Characterization of 23 small supernumerary marker chromosomes detected at pre-natal diagnosis: The value of fluorescence in situ hybridizationE Manolakos, K Kefalas, R Neroutsou, et al.International Journal of Molecular Medicine|May 10, 2007
Forty-eight new cases with infertility due to balanced chromosomal rearrangements: detailed molecular cytogenetic analysis of the 90 involved breakpointsM Manvelyan, I Schreyer, I Höls-Herpertz, et al.American Journal of Human Genetics|December 12, 2000
Genotypic and phenotypic spectrum in tricho-rhino-phalangeal syndrome types I and IIIH J Lüdecke, J Schaper, P Meinecke, et al.Pageof 26