Preimplantation diagnosis of genetic and chromosomal disorders
- 1 May 1994
- journal article
- review article
- Published by Springer Nature in Journal of Assisted Reproduction and Genetics
- Vol. 11 (5) , 236-243
- https://doi.org/10.1007/bf02214343
Abstract
No abstract availableThis publication has 29 references indexed in Scilit:
- Homeobox gene expression in human oocytes and preembryosMolecular Reproduction and Development, 1995
- Chromosome Mosaicism in Human EmbryosBiology of Reproduction, 1994
- Preimplantation single cell analyses of dystrophin gene deletions using whole genome amplificationNature Genetics, 1994
- Polymerase chain reaction analysis of the cystic fibrosis ΔF508 mutation in human blastomeres following oocyte injection of a single sperm from a carrierPrenatal Diagnosis, 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
- Current progress in preimplantation genetic diagnosisJournal of Assisted Reproduction and Genetics, 1993
- Okadaic acid induces premature chromosome condensation reflecting the cell cycle progression in one‐cell stage mouse embryosMolecular Reproduction and Development, 1993
- A fast and efficient method for simultaneous X and Y in situ hybridization of human blastomeresJournal of Assisted Reproduction and Genetics, 1993
- Comparative Genomic Hybridization for Molecular Cytogenetic Analysis of Solid TumorsScience, 1992
- Preconception and preimplantation diagnosis for cystic fibrosisPrenatal Diagnosis, 1992