Molecular cytogenetic analysis by genomic hybridization to determine the cause of recurrent miscarriage Aurore Perrin, Ph.D., Bruno Delobel, M.D., Joris.

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Molecular cytogenetic analysis by genomic hybridization to determine the cause of recurrent miscarriage Aurore Perrin, Ph.D., Bruno Delobel, M.D., Joris Andrieux, M.D., Ph.D., Philippe Gosset, M.D., Nadia Gueganic, B.Sc., Florence Petit, M.D., Marc De Braekeleer, M.D., Ph.D., Frédéric Morel, Ph.D. Fertility and Sterility Volume 93, Issue 6, Pages 2075.e3-2075.e6 (April 2010) DOI: 10.1016/j.fertnstert.2009.11.016 Copyright © 2010 American Society for Reproductive Medicine Terms and Conditions

Figure 1 Pedigree of the carrier of the t(2;6)(q35;q24). The proband (III-2), his son (IV-4), the proband's father (II-2), and his brother (III-5) have the same chromosomal abnormality. Fertility and Sterility 2010 93, 2075.e3-2075.e6DOI: (10.1016/j.fertnstert.2009.11.016) Copyright © 2010 American Society for Reproductive Medicine Terms and Conditions

Figure 2 (A, B) Array-CGH detected a genomic microdeletion at the 6q24.3 breakpoint in the peripheral blood lymphocytes of the father and his son. (C, D) The size of the microdeletion on the der(6) was 1.3 Mb in the peripheral blood lymphocytes of the father and his son. Fertility and Sterility 2010 93, 2075.e3-2075.e6DOI: (10.1016/j.fertnstert.2009.11.016) Copyright © 2010 American Society for Reproductive Medicine Terms and Conditions