Presence of chromosomal mosaicism in abnormal preimplantation embryos detected by fluorescence in situ hybridisation
- 1 December 1994
- journal article
- Published by Springer Nature in Human Genetics
- Vol. 94 (6) , 609-615
- https://doi.org/10.1007/bf00206952
Abstract
No abstract availableKeywords
This publication has 24 references indexed in Scilit:
- Fertilization and early embryology: Diagnosis of major chromosome aneuploidies in human preimplantation embryosHuman Reproduction, 1993
- Preimplantation prevention of X-linked disease: reliable and rapid sex determination of single human cells by restriction analysis of simultaneously amplified ZFX and ZFY sequencesHuman Molecular Genetics, 1993
- Binucleate blastomeres in preimplantation human embryos in vitro: failure of cytokinesis during early cleavageReproduction, 1993
- Cytogenetic and morphological observations of single pronucleated human oocytes after in-vitro fertilizationHuman Reproduction, 1993
- Dual fluorescent in situ hybridisation for simultaneous detection of X and Y chromosome-specific probes for the sexing of human preimplantation embryonic nucleiHuman Genetics, 1992
- Triploidy after in vitro fertilization: Cytogenetic analysis of human zygotes and embryosJournal of Assisted Reproduction and Genetics, 1992
- Fluorescent in-situ hybridization to interphase nuclei of human preimplantation embryos with X and Y chromosome specific probesHuman Reproduction, 1991
- Chromosome investigations in early life. II. Human preimplantation embryosHuman Reproduction, 1987
- Characterisation of a human Y chromosome repeated sequence and related sequences in higher primatesChromosoma, 1982
- Cloning of human satellite III DNA: different components are on different chromosomesNucleic Acids Research, 1979