Polar body biopsy

Preimplantation Genetic Diagnosis, Second Edition

Volumn , Issue , 2009, Pages 166-174

  Montag, Markus ^a   Van Der Ven, Katrin ^a   Van Der Ven, Hans ^a  

^a UNIVERSITY OF BONN   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 78650683807     PISSN: None     EISSN: None     Source Type: Book    
DOI: 10.1017/CBO9780511581571.010     Document Type: Chapter

References (14)

1. American Society for Reproductive Medicine (ASRM). Sex selection and preimplantation genetic diagnosis. Ethics Committee of the American Society of Reproductive Medicine. Fertility and Sterility 1999; 72: 595-8.
2. Fugger EF, Black SH, Keyvanfar K and Schulman JD. Births of normal daughters after MicroSort sperm separation and intrauterine insemination, in vitro fertilization, or intracytoplasmic sperm injection. Human Reproduction1998;13:2367-70.
3. Gigarel N, Frydman N, Burlet P et al. Single cell co-amplification of polymorphic markers for the indirect preimplantation genetic diagnosis of hemophilia A, X-linked adrenoleukodystrophy, X-linked hydrocephalus and incontinentia pigmenti loci on Xq28. Human Genetics 2004; 114:298-305.
4. Goossens V, Harton G, Moutou C et al. ESHRE PGD Consortium data collection VIII: cycles from January to December 2005 with pregnancy follow-up to October 2006. Human Reproduction 2008; 23: 2629-45.
5. Griffin DK, Handyside AH, Harper JC et al. Clinical experience with preimplantation genetic diagnosis of sex by dual fluorescent in situ hybridization. Journal of Assisted Reproduction and Genetics 1994; 11: 132-43.
6. Handyside AH, Kontogianni EH, Hardy K and Winston RM. Pregnancies from biopsied human preimplantation embryos sexed by Y-specific DNA amplification. Nature1990; 344: 768-70.
7. Hardy K and Handyside AH. Biopsy of cleavage stage human embryos and diagnosis of single gene defects by DNA amplification. Archives of Pathology and Laboratory Medicine1992; 116: 388-92.
8. Malmgren H, White I, Johansson S et al. PGD for dystrophin gene deletions using fluorescence in situ hybridization. Molecular Human Reproduction 2006; 12: 353-6.
9. Munne S, Tang YX, Grifo J, Rosenwaks Z and Cohen J. Sex determination of human embryos using the polymerase chain reaction and confirmation by fluorescence in situ hybridization. FertilityandSterility 1994; 61:111-17.
10. Online Mendelian Inheritance in Man (OMIM)™, McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University (Baltimore, MD), and National Center for Biotechnology Information, National Library of Medicine (Bethesda, MD) (September 14, 2007). (Available online at: www.ncbi.nlm.nih.gov/omim).
11. Renwick PJ, Trussler J, Ostad-Saffari E et al. Proof of principle and first cases using preimplantation genetic haplotyping - a paradigm shift for embryo diagnosis. Reproductive Biomedicine Online2006; 13:110-19.
12. Sermon KD, Michiels A, Harton G et al. ESHRE PGD Consortium data collection IV: cycles from January to December 2003 with pregnancy follow-up to October 2004. Human Reproduction 2007; 22: 323-6.
13. Thornhill AR, de Die-Smulders CE, Geraedts JP et al.ESHRE PGD Consortium “Best practice guidelines for clinical preimplantation genetic diagnosis (PGD) and preimplantation genetic screening (PGS)”. Human Reproduction 2005; 20: 35-48.
14. Verlinsky Y, Rechitsky S, Verlinsky O et al. Polar body-based preimplantation diagnosis for X-linked disorders. Reproductive Biomedicine Online2002; 4: 38-42.