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Familial pericentric inversion of chromosome 18: behavioral abnormalities in patients heterozygous for either the dup(18p)/del(18q) or dup(18q)/del(18p) recombinant chromosome
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Subtelomeric familial translocation t(2;7)(q37;q35) leading to partial trisomy 7q35 -> qter: Molecular cytogenetic analysis and clinical phenotype in two generations.
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Fluorescent in-situ hybridization on human embryos showing cleavage arrest after freezing and thawing
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Application of fluorescence in situ hybridization to the identification of different marker chromosomes.
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Numerieke chromosomale afwijkingen in zaadcellen van patiënten met oligosthenoateratozoospermia
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Triple colour fluorescent in-situ hybridization for chromosomes X, Y and 1 on spare human embryos.
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Mosaic tetrasomy 15q25->qter in a newborn infant with multiple anomalies.
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Why karyotype cystic hygroma cells.
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Proximal deletion of chromosome-21 confirmed by in-situ hybridization and molecular studies.
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Tubal hydatiform mole.
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MOLECULAR CYTOGENETIC CHARACTERIZATION OF MARKER CHROMOSOMES FOUND AT PRENATAL-DIAGNOSIS.
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Detection of subtle reciprocal translocations by fluorescence in situ hibridization.
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De ovariële functie bij het Turner syndroom
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Chromosome analysis in human oocytes unfertilized in vitro : a mathematical model for the estimation of the first meiotic non-disjunction frequency
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A 45,X/46/XX/47,XXX female mosaic diagnosed by cytogenetic analysis of unfertilized in vitro fertilization oocytes. ESHRE Congress, abstract nr. 115, Den Haag, 8-11 juli, 1992.
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De cytogenetica en foetale outcome van hygroma colli. Gyna&eia 3/7, 1998, 208-211.
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Numerieke chromosomale afwijkingen in patiënten met oligoasthenozoöspermie . Annalen van de Veren. Voor Fertiliteitsstudie 1997, 24, 30-32.