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European Journal of Human Genetics : EJHG|October 20, 2000
Inv dup(22), del(22)(q11) and r(22) in the father of a child with DiGeorge syndromeA Bergman, E BlennowJournal of Medical Genetics|May 1, 1996
Small extra ring chromosome derived from chromosome 10p: clinical report and characterisation by FISHE Blennow, E TillbergJournal of Medical Genetics|May 1, 1990
Partial monosomy 8p with minimal dysmorphic signsE Blennow, K Bröndum-NielsenClinical Genetics|June 1, 1991
Molecular identification of a small supernumerary marker chromosome by in situ hybridization: diagnosis of an isochromosome 18p with probe L1.84E Blennow, K B NielsenSeminars in Fetal & Neonatal Medicine|December 24, 2010
Preimplantation genetic diagnosis: twenty years of practiceE Iwarsson, H Malmgren, E BlennowAmerican Journal of Medical Genetics|October 21, 1999
Maternal isodisomy of chromosome 9 with no impact on the phenotype in a woman with two isochromosomes: i(9p) and i(9q)E J Björck, B M Anderlid, E BlennowDiagnostic Molecular Pathology : the American Journal of Surgical Pathology, Part B|March 30, 2001
Physical state of HPV16 and chromosomal mapping of the integrated form in cervical carcinomasM Kalantari, E Blennow, B Hagmar, et al.American Journal of Medical Genetics|October 2, 1996
Monosomy 1p36.31-33-->pter due to a paternal reciprocal translocation: prognostic significance of FISH analysisE Blennow, T H Bui, A Wallin, et al.Haematologica|November 6, 2001
Molecular cytogenetic characterization of acute myeloid leukemia and myelodysplastic syndromes with multiple chromosome rearrangementsC Lindvall, M Nordenskjöld, A Porwit, et al.British Journal of Haematology|September 21, 2001
Interphase fluorescence in situ hybridization and spectral karyotyping reveals hidden genetic aberrations in children with acute lymphoblastic leukaemia and a normal banded karyotypeA Nordgren, J Schoumans, S Söderhäll, et al.Pageof 6