TY - JOUR AU - Benn, P. AU - Cuckle, H. AU - Pergament, E. PY - 2013 DA - 2013// TI - Non-invasive prenatal testing for aneuploidy: current status and future prospects JO - Ultrasound Obstet Gynecol VL - 42 UR - https://doi.org/10.1002/uog.12513 DO - 10.1002/uog.12513 ID - Benn2013 ER - TY - JOUR AU - Song, Y. AU - Liu, C. AU - Qi, H. AU - Zhang, Y. AU - Bian, X. AU - Liu, J. PY - 2013 DA - 2013// TI - Noninvasive prenatal testing of fetal aneuploidies by massively parallel sequencing in a prospective Chinese population JO - Prenat Diagn VL - 33 UR - https://doi.org/10.1002/pd.4160 DO - 10.1002/pd.4160 ID - Song2013 ER - TY - JOUR AU - Bianchi, D. W. AU - Parker, R. L. AU - Wentworth, J. AU - Madankumar, R. AU - Saffer, C. AU - Das, A. F. PY - 2014 DA - 2014// TI - DNA sequencing versus standard prenatal aneuploidy screening JO - N Engl J Med VL - 370 UR - https://doi.org/10.1056/NEJMoa1311037 DO - 10.1056/NEJMoa1311037 ID - Bianchi2014 ER - TY - JOUR PY - 2012 DA - 2012// TI - Committee opinion No. 545: noninvasive prenatal testing for fetal aneuploidy JO - Obstet Gynecol VL - 120 ID - ref4 ER - TY - JOUR AU - Liang, D. AU - Lv, W. AU - Wang, H. AU - Xu, L. AU - Liu, J. AU - Li, H. PY - 2013 DA - 2013// TI - Non-invasive prenatal testing of fetal whole chromosome aneuploidy by massively parallel sequencing JO - Prenat Diagn VL - 33 UR - https://doi.org/10.1002/pd.4033 DO - 10.1002/pd.4033 ID - Liang2013 ER - TY - JOUR AU - Song, Y. AU - Huang, S. AU - Zhou, X. AU - Jiang, Y. AU - Qi, Q. AU - Bian, X. PY - 2015 DA - 2015// TI - Non-invasive prenatal testing for fetal aneuploidies in the first trimester of pregnancy JO - Ultrasound Obstet Gynecol VL - 45 UR - https://doi.org/10.1002/uog.13460 DO - 10.1002/uog.13460 ID - Song2015 ER - TY - STD TI - ISCN 2013. An International System for Human Cytogenetic Nomenclature (2013). Editors: L.g. Shaffer, J McGowen, M. Schmid. Publisher: Karger, Basel, Switzerland. ID - ref7 ER - TY - JOUR AU - Feingold, M. AU - Atkins, L. PY - 1973 DA - 1973// TI - A case of trisomy 9 JO - J Med Genet VL - 10 UR - https://doi.org/10.1136/jmg.10.2.184 DO - 10.1136/jmg.10.2.184 ID - Feingold1973 ER - TY - JOUR AU - Haslam, R. H. AU - Broske, S. P. AU - Moore, C. M. AU - Thomas, G. H. AU - Neill, C. A. PY - 1973 DA - 1973// TI - Trisomy 9 mosaicism with multiple congenital anomalies JO - J Med Genet VL - 10 UR - https://doi.org/10.1136/jmg.10.2.180 DO - 10.1136/jmg.10.2.180 ID - Haslam1973 ER - TY - JOUR AU - Arnold, G. L. AU - Kirby, R. S. AU - Stern, T. P. AU - Sawyer, J. R. PY - 1995 DA - 1995// TI - Trisomy 9: review and report of two new cases JO - Am J Med Genet VL - 56 UR - https://doi.org/10.1002/ajmg.1320560303 DO - 10.1002/ajmg.1320560303 ID - Arnold1995 ER - TY - JOUR AU - Bruns, D. PY - 2011 DA - 2011// TI - Presenting physical characteristics, medical conditions, and developmental status of long-term survivors with trisomy 9 mosaicism JO - Am J Med Genet A VL - 155A UR - https://doi.org/10.1002/ajmg.a.33928 DO - 10.1002/ajmg.a.33928 ID - Bruns2011 ER - TY - JOUR AU - Sherer, D. M. AU - Wang, N. AU - Thompson, H. O. AU - Peterson, J. C. AU - Miller, M. E. AU - Metlay, L. A. PY - 1992 DA - 1992// TI - An infant with trisomy 9 mosaicism presenting as a complete trisomy 9 by amniocentesis JO - Prenat Diagn VL - 12 UR - https://doi.org/10.1002/pd.1970120105 DO - 10.1002/pd.1970120105 ID - Sherer1992 ER - TY - JOUR AU - Pfeiffer, R. A. AU - Ulmer, R. AU - Kniewald, A. AU - Wagner-Thiessen, E. PY - 1984 DA - 1984// TI - Prenatal diagnosis of trisomy 9 mosaicism possibly limited to fetal membranes JO - Prenat Diagn VL - 4 UR - https://doi.org/10.1002/pd.1970040511 DO - 10.1002/pd.1970040511 ID - Pfeiffer1984 ER - TY - JOUR AU - Smoleniec, J. S. AU - Davies, T. AU - Lunt, P. AU - Berry, P. J. AU - James, D. PY - 1993 DA - 1993// TI - Complex mosaicism associated with trisomy 9 JO - Prenat Diagn VL - 13 UR - https://doi.org/10.1002/pd.1970130308 DO - 10.1002/pd.1970130308 ID - Smoleniec1993 ER - TY - JOUR AU - Harper, J. C. AU - Wilton, L. AU - Traeger-Synodinos, J. AU - Goossens, V. AU - Moutou, C. AU - SenGupta, S. B. PY - 2012 DA - 2012// TI - The ESHRE PGD consortium: 10 years of data collection JO - Hum Reprod Update VL - 18 UR - https://doi.org/10.1093/humupd/dmr052 DO - 10.1093/humupd/dmr052 ID - Harper2012 ER - TY - JOUR AU - Taylor, T. H. AU - Gitlin, S. A. AU - Patrick, J. L. AU - Crain, J. L. AU - Wilson, J. M. AU - Griffin, D. K. PY - 2014 DA - 2014// TI - The origin, mechanisms, incidence and clinical consequences of chromosomal mosaicism in humans JO - Hum Reprod Update VL - 20 UR - https://doi.org/10.1093/humupd/dmu016 DO - 10.1093/humupd/dmu016 ID - Taylor2014 ER - TY - JOUR AU - Eggermann, T. AU - Soellner, L. AU - Buiting, K. AU - Kotzot, D. PY - 2015 DA - 2015// TI - Mosaicism and uniparental disomy in prenatal diagnosis JO - Trens Mol Med VL - 21 UR - https://doi.org/10.1016/j.molmed.2014.11.010 DO - 10.1016/j.molmed.2014.11.010 ID - Eggermann2015 ER - TY - JOUR AU - Wilkinson, T. A. AU - James, R. S. AU - Crolla, J. A. AU - Cockwell, A. E. AU - Campbell, P. L. AU - Temple, I. K. PY - 1996 DA - 1996// TI - A case of maternal uniparental disomy of chromosome 9 in association with confined placental mosaicism for trisomy 9 JO - Prenat Diagn VL - 16 UR - https://doi.org/3.0.CO;2-S DO - 3.0.CO;2-S ID - Wilkinson1996 ER - TY - JOUR AU - Slater, H. R. AU - Ralph, A. AU - Daniel, A. AU - Worthington, S. AU - Roberts, C. PY - 2000 DA - 2000// TI - A case of maternal uniparental disomy of chromosome 9 diagnosed prenatally and the related problem of residual trisomy JO - Prenat Diagn VL - 20 UR - https://doi.org/3.0.CO;2-E DO - 3.0.CO;2-E ID - Slater2000 ER - TY - JOUR AU - Morison, I. M. AU - Reeve, A. E. PY - 1998 DA - 1998// TI - A catalogue of imprinted genes and parent-of-origin effects in humans and animals JO - Hum Mol Genet VL - 7 UR - https://doi.org/10.1093/hmg/7.10.1599 DO - 10.1093/hmg/7.10.1599 ID - Morison1998 ER - TY - JOUR AU - Hagen, C. B. AU - Eiklid, K. AU - Orstavik, K. H. AU - Braaten, O. AU - Prescott, T. AU - Kroken, M. PY - 2003 DA - 2003// TI - Prenatally diagnosed trisomy 9 mosaicism and paternal uniparental disomy 9 in the child JO - Europ J Hum Genet VL - 11 ID - Hagen2003 ER - TY - STD TI - Cooper GM, Coe BP, Girirajan S, Rosenfeld JA, Vu TH, Baker C et al. A copy number variation morbidity map of developmental delay. Nat Genet. 2011;43:838–46. ID - ref22 ER - TY - JOUR AU - Zadeh, T. M. AU - Peters, J. AU - Sandlin, C. PY - 1987 DA - 1987// TI - Prenatal diagnosis of mosaic trisomy 9 JO - Prenat Diagn VL - 7 UR - https://doi.org/10.1002/pd.1970070110 DO - 10.1002/pd.1970070110 ID - Zadeh1987 ER - TY - JOUR AU - Schwartz, S. AU - Ashai, S. AU - Meijboom, E. J. AU - Schwartz, M. F. AU - Sun, C. C. AU - Cohen, M. M. PY - 1989 DA - 1989// TI - Prenatal detection of trisomy 9 mosaicism JO - Prenat Diagn VL - 9 UR - https://doi.org/10.1002/pd.1970090803 DO - 10.1002/pd.1970090803 ID - Schwartz1989 ER - TY - JOUR AU - Merino, A. AU - Perdigo, A. AU - Nombalais, F. AU - Yvinec, M. AU - Roux, M. G. AU - Bellec, V. PY - 1993 DA - 1993// TI - Prenatal diagnosis of trisomy 9 mosaicism: two new cases JO - Prenat Diagn VL - 13 UR - https://doi.org/10.1002/pd.1970131016 DO - 10.1002/pd.1970131016 ID - Merino1993 ER - TY - JOUR AU - Kosaki, R. AU - Hanai, S. AU - Kakishima, H. AU - Okada, M. A. AU - Hayashi, S. AU - Ito, Y. PY - 2006 DA - 2006// TI - Discrepancies in cytogenetic results between amniocytes and postnatally obtained blood: trisomy 9 mosaicism JO - Congenit Anom (Kyoto) VL - 46 UR - https://doi.org/10.1111/j.1741-4520.2006.00111.x DO - 10.1111/j.1741-4520.2006.00111.x ID - Kosaki2006 ER - TY - JOUR AU - Daniel, A. AU - Wu, Z. AU - Darmanian, A. AU - Malafiej, P. AU - Tembe, V. AU - Peters, G. PY - 2004 DA - 2004// TI - Issues arising from the prenatal diagnosis of some rare trisomy mosaics–the importance of cryptic fetal mosaicism JO - Prenat Diagn VL - 24 UR - https://doi.org/10.1002/pd.936 DO - 10.1002/pd.936 ID - Daniel2004 ER - TY - JOUR AU - Pham, J. AU - Shaw, C. AU - Pursley, A. AU - Hixson, P. AU - Sampath, S. AU - Roney, E. PY - 2014 DA - 2014// TI - Somatic mosaicism detected by exon-targeted, high-resolution aCGH in 10,362 consecutive cases JO - Eur J Hum Genet VL - 22 UR - https://doi.org/10.1038/ejhg.2013.285 DO - 10.1038/ejhg.2013.285 ID - Pham2014 ER - TY - JOUR AU - Berry, A. C. AU - Mutton, D. E. AU - Lewis, D. G. PY - 1978 DA - 1978// TI - Mosaicism and the trisomy 8 syndrome JO - Clin Genet VL - 14 UR - https://doi.org/10.1111/j.1399-0004.1978.tb02114.x DO - 10.1111/j.1399-0004.1978.tb02114.x ID - Berry1978 ER - TY - JOUR AU - Wolstenholme, J. PY - 1996 DA - 1996// TI - Confined placental mosaicism for trisomies 2, 3, 7, 8, 9, 16, and 22: their incidence, likely origins, and mechanisms for cell lineage compartmentalization JO - Prenat Diagn VL - 16 UR - https://doi.org/3.0.CO;2-8 DO - 3.0.CO;2-8 ID - Wolstenholme1996 ER - TY - JOUR AU - Li, H. AU - Durbin, R. PY - 2009 DA - 2009// TI - Fast and accurate short read alignment with burrows- wheeler transform JO - Bioinformatics VL - 25 UR - https://doi.org/10.1093/bioinformatics/btp324 DO - 10.1093/bioinformatics/btp324 ID - Li2009 ER -