Triple colour fluorescent in-situ hybridization for chromosomes X,Y and 1 on spare human embryos.

By Laverge H   De Sutter P   Verschraegen-Spae M R   De Paepe A   Dhont M  

Human Reproduction, Vol. 12, Iss. 4, 1997-04 ,pp. : 809-814

Oxford University Press

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Genetics. Preliminary study of the incidence of disomy in sperm fractions after MicroSort flow cytometry

By Vidal F.  

Human Reproduction, Vol. 14, Iss. 12, 1999-12 ,pp. : 2987-2990

Oxford University Press

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Analysis of human sperm-derived pronuclei by three-colour fluorescent in-situ hybridization.

By Martínez-Pasarell O   Márquez C   Coll M D   Egozcue J   Templado C  

Human Reproduction, Vol. 12, Iss. 4, 1997-04 ,pp. : 641-645

Oxford University Press

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Sperm aneuploidy in fathers of Klinefelter’s syndrome offspring assessed by multicolour fluorescent in situ hybridization using probes for chromosomes 6, 13, 18, 21, 22, X and Y

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Human Reproduction, Vol. 21, Iss. 2, 2006-02 ,pp. : 524-528

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Incidence of chromosome 21 disomy in human spermatozoa as determined by fluorescent in-situ hybridization

By Blanco J.   Egozcue J.   Vidal F.  

Human Reproduction, Vol. 11, Iss. 4, 1996-04 ,pp. : 722-726

Oxford University Press

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