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Clinical Neurology and Neurosurgery|January 1, 1988
Familial meningioma. Case report with cytogenetic studyW Van Landegem, A Vakaet, A De Paepe, et al.Clinical Genetics|April 1, 1992
Familial Turner syndromeM R Verschraegen-Spae, H Depypere, F Speleman, et al.Human Reproduction (Oxford, England)|April 1, 1997
Triple colour fluorescent in-situ hybridization for chromosomes X,Y and 1 on spare human embryosH Laverge, P De Sutter, M R Verschraegen-Spae, et al.Prenatal Diagnosis|May 1, 1993
Molecular cytogenetic characterization of marker chromosomes found at prenatal diagnosisM R Verschraegen-Spae, N van Roy, A de Perdigo, et al.Annales De Genetique|May 26, 1998
Application of fluorescence in situ hybridization to the identification of different marker chromosomesM R Verschraegen-Spae, B Quack, S Rousseaux, et al.Human Reproduction (Oxford, England)|April 29, 1998
Fluorescent in-situ hybridization on human embryos showing cleavage arrest after freezing and thawingH Laverge, J Van der Elst, P De Sutter, et al.American Journal of Medical Genetics|December 1, 1991
Pallister-Killian syndrome: characterization of the isochromosome 12p by fluorescent in situ hybridizationF Speleman, J G Leroy, N Van Roy, et al.Annales De Genetique|January 1, 1992
Interstitial deletion and ring chromosome derived from 19q. Proximal 19q trisomy phenotypeB Quack, N Van Roy, M R Verschraegen-Spae, et al.American Journal of Obstetrics and Gynecology|July 1, 1993
Tubal hydatidiform moleH T Depypere, M Dhont, M R Verschraegen-Spae, et al.Human Genetics|January 1, 1986
The significance of pericentric inversions of chromosome 2M Djalali, P Steinbach, J Bullerdiek, et al.Pageof 15