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Koehler U, Schoen U, Mayer V, Holinski-Feder E Preimplantation Genetic Diagnosis for Monogenic Disorders and Chromosomal Rearrangements – The German Perspective Journal für Reproduktionsmedizin und Endokrinologie - Journal of Reproductive Medicine and Endocrinology 2013; 10 (Sonderheft 1): 38-44 Volltext (PDF) Summary Übersicht
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Abbildung 1: Polar body diagnosis for haemophilia A Polar body diagnosis for haemophilia A: fragment length analysis of amplified polymorphic markers of the carrier mother and of PB I and PB II. Arrows indicate polymorphic marker alleles linked to the mutation. The detection of the wild type haplotype in PB I and the haplotype linked to the mutation in PB II indicates the presence of the mutation in the oocyte. |
Abbildung 1: Polar body diagnosis for haemophilia A
Polar body diagnosis for haemophilia A: fragment length analysis of amplified polymorphic markers of the carrier mother and of PB I and PB II. Arrows indicate polymorphic marker alleles linked to the mutation. The detection of the wild type haplotype in PB I and the haplotype linked to the mutation in PB II indicates the presence of the mutation in the oocyte. |