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Cytogenetic and Genome Research|April 4, 2013
First report of a small supernumerary der(8;14) marker chromosomeR S Guilherme, A R N Dutra, A B A Perez, et al.Cytogenetic and Genome Research|March 2, 2012
Five novel locations of Neocentromeres in human: 18q22.1, Xq27.1∼27.2, Acro p13, Acro p12, and heterochromatin of unknown originE Klein, M Rocchi, A Ovens-Raeder, et al.Human Genetics|March 7, 1998
Juvenile open angle glaucoma: fine mapping of the TIGR gene to 1q24.3-q25.2 and mutation analysisK G Michels-Rautenstrauss, C Y Mardin, W M Budde, et al.Balkan Journal of Medical Genetics : BJMG|November 23, 2013
Human Ring Chromosomes - New Insights for their Clinical SignificanceRs Guilherme, E Klein, Ab Hamid, et al.Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|April 9, 2008
Small supernumerary marker chromosomes (sSMC) in patients with a 45,X/46,X,+mar karyotype - 17 new cases and a review of the literatureT Liehr, K Mrasek, S Hinreiner, et al.Molecular Syndromology|November 1, 2012
Shared Copy Number Variation in Simultaneous Nephroblastoma and Neuroblastoma due to Fanconi AnemiaA Serra, K Eirich, A K Winkler, et al.Journal of Medical Genetics|January 1, 1997
Detection of the CMT1A/HNPP recombination hotspot in unrelated patients of European descentV Timmerman, B Rautenstrauss, L T Reiter, et al.Cancer Genetics|January 2, 2022
Somatic homozygous loss of SH2B3, and a non-Robertsonian translocation t(15;21)(q25.3;q22.1) with NTRK3 rearrangement, in an adolescent with progenitor B-cell acute lymphoblastic leukemia with the iAMP21R R Capela de Matos, Mak Othman, G M Ferreira, et al.Cytogenetic and Genome Research|April 11, 2012
Tetrasomy 9p mosaicism associated with a normal phenotype in two casesI Papoulidis, M Kontodiou, M Tzimina, et al.Cytogenetic and Genome Research|September 7, 2006
Duplications of proximal 16q flanked by heterochromatin are not euchromatic variants and show no evidence of heterochromatic position effectJ C K Barber, S Zhang, N Friend, et al.Pageof 26