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  1. 1
    A. Marx-Deseure, S. Carpentier, D. Thomas, S. Bouquillon, B. Delobel, B. Bailleux, H. Bomy, P. Vaast, V. Debarge, Naissance d’un enfant porteur de trisomie 21 : choix parental ou défaut de la politique de dépistage ?, Gynécologie Obstétrique & Fertilité, 2015, 43, 4, 284

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  2. 2
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  3. 3
    D. G. Iliescu, M. L. Cara, S. Tudorache, P. Antsaklis, L. V. Novac, A. Antsaklis, N. Cernea, Agenesis of ductus venosus in sequential first and second trimester screening, Prenatal Diagnosis, 2014, 34, 11
  4. 4
    S. Viaux-Savelon, M. Dommergues, D. Cohen, Dépistage échographique anténatal des anomalies mineures de bon pronostic : impact émotionnel, représentations parentales et relation mère-enfant, Revue de médecine périnatale, 2014, 6, 3, 199

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  5. 5
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  6. 6
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  7. 7
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  8. 8
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  9. 9
    C. Coulon, Ph. Bourgeot, Y. Robert, P. Vaast, V. Debarge, B. Guérin, Échographie en pratique obstétricale, 2014,

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  10. 10
    B. Guérin, Ph. Bourgeot, Y. Robert, Ph. Coquel, Échographie en pratique obstétricale, 2014,

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  11. 11
    Antoine Guedeney, Julie Le Foll, Laure Vannier, Sylvie Viaux-Savelon, Jaqueline Wendland, Petite enfance et psychopathologie, 2014,

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  12. You have free access to this content12
    K. M. Orzechowski, V. Berghella, Isolated fetal pyelectasis and the risk of Down syndrome: a meta-analysis, Ultrasound in Obstetrics & Gynecology, 2013, 42, 6
  13. You have free access to this content13
    M. Agathokleous, P. Chaveeva, L. C. Y. Poon, P. Kosinski, K. H. Nicolaides, Meta-analysis of second-trimester markers for trisomy 21, Ultrasound in Obstetrics & Gynecology, 2013, 41, 3
  14. 14
    Cynthia J. Curry, Emery and Rimoin's Principles and Practice of Medical Genetics, 2013,

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  15. 15
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  16. 16
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  17. 17
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  18. 18
    P. Bourgeot, Échographie obstétricale en routine des deuxième et troisième trimestres, EMC - Radiologie et imagerie médicale - Génito-urinaire - Gynéco-obstétricale - Mammaire, 2012, 7, 4, 1

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  19. 19
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  20. 20
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    CrossRef

  21. 21
    Mohammed Khairy Ali, Sherif A. Shazly, Ali H. Ali, Ahmed Y. Abdelbadee, Ahmed M. Abbas, Ultrasonographic soft markers of aneuploidy in second trimester fetuses, Middle East Fertility Society Journal, 2012, 17, 3, 145

    CrossRef

  22. 22
    A.-S. Weingertner, N.-T. Trieu, M. Kohler, B. Viville, G. Levy, Y. Montaya, R. Kutnahorsky, I. Tissier, A. Kohler, M. Tanghe, C. Mager, E. Benassi, M. Cancelier, M. Neuman, N. Bouffet, M.C. Hunsinger, F. Hornecker, B. Langer, I. Nisand, R. Favre, Dépistage combiné de la trisomie 21 au premier trimestre : à propos de cinq ans d’expérience prospective multicentrique, La Revue Sage-Femme, 2011, 10, 2, 72

    CrossRef

  23. 23
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  24. 24
    M. Krapp, A. Ludwig, Pränatale Detektion fetaler chromosomaler Aberrationen im 1. und 2. Trimenon, medizinische genetik, 2011, 23, 4, 444

    CrossRef

  25. 25
    Jeanine F. Carbone, Methodius G. Tuuli, Jeffrey M. Dicke, George A. Macones, Anthony O. Odibo, Revisiting the risk for aneuploidy in fetuses with isolated pyelectasis, Prenatal Diagnosis, 2011, 31, 6
  26. 26
    Kirsten Salmeen, Marya Zlatnik, The Oldest Gravidas: A Review of Pregnancy Risks in Women Over 45, Obstetrical & Gynecological Survey, 2011, 66, 9, 580

    CrossRef

  27. 27
    Marc Dommergues, Rodrigo Ruano, Marie-Cécile Aubry, High Risk Pregnancy, 2011,

    CrossRef

  28. 28
    A.-S. Weingertner, N.-T. Trieu, M. Kohler, B. Viville, G. Levy, Y. Montaya, R. Kutnahorsky, I. Tissier, A. Kohler, M. Tanghe, C. Mager, E. Benassi, M. Cancelier, M. Neuman, N. Bouffet, M.C. Hunsinger, F. Hornecker, B. Langer, I. Nisand, R. Favre, Dépistage combiné de la trisomie 21 au premier trimestre : à propos de cinq ans d’expérience prospective multicentrique, Journal de Gynécologie Obstétrique et Biologie de la Reproduction, 2010, 39, 5, 353

    CrossRef

  29. 29
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    CrossRef

  30. 30
    Hyun Jin Cho, Hye-Sung Won, Jae-Yun Sim, Pil-Ryang Lee, Ahm Kim, Evaluation of the usefulness of the fetal femur length and humeral length to detect Down syndrome in Korean subjects, Korean Journal of Obstetrics and Gynecology, 2010, 53, 11, 967

    CrossRef

  31. 31
    H. J. Cho, H. S. Won, D. H. Ju, H. J. Roh, P. R. Lee, A. Kim, Evaluation of the usefulness of the fetal femur length with respect to gestational age to detect Down syndrome in Korean subjects, Prenatal Diagnosis, 2010, 30, 8
  32. You have free access to this content32
    G. R. DeVore, Genetic sonography: the historical and clinical role of fetal echocardiography, Ultrasound in Obstetrics & Gynecology, 2010, 35, 5
  33. 33
    Kjersti M. Aagaard-Tillery, T. Flint Porter, Fergal D. Malone, David A. Nyberg, Jamie Collins, Christine H. Comstock, Gary Hankins, Keith Eddleman, Lorraine Dugoff, Honor M. Wolfe, Mary E. D'Alton, Influence of maternal BMI on genetic sonography in the FaSTER trial, Prenatal Diagnosis, 2010, 30, 1
  34. 34
    Diane Timms, Winston A. Campbell, Modifying Risk for Aneuploidy with Second-Trimester Ultrasound After a Positive Serum Screen, Clinics in Laboratory Medicine, 2010, 30, 3, 677

    CrossRef

  35. 35
    A. Geipel, A. Willruth, J. Vieten, U. Gembruch, C. Berg, Nuchal fold thickness, nasal bone absence or hypoplasia, ductus venosus reversed flow and tricuspid valve regurgitation in screening for trisomies 21, 18 and 13 in the early second trimester, Ultrasound in Obstetrics & Gynecology, 2010, 35, 5
  36. 36
    Dagmar Tapon, Prenatal Testing for Down Syndrome: Comparison of Screening Practices in the UK and USA, Journal of Genetic Counseling, 2010, 19, 2, 112

    CrossRef

  37. 37
    Anna-Karin Larsson, Elizabeth Crang-Svalenius, Anna-Karin Dykes, Information for better or for worse: interviews with parents when their foetus was found to have choroid plexus cysts at a routine second trimester ultrasound, Journal of Psychosomatic Obstetrics & Gynecology, 2009, 30, 1, 48

    CrossRef

  38. 38
    Deborah A. Driscoll, Susan Gross, Prenatal Screening for Aneuploidy, New England Journal of Medicine, 2009, 360, 24, 2556

    CrossRef

  39. 39
    Kjersti M. Aagaard-Tillery, Fergal D. Malone, David A. Nyberg, T Flint Porter, Howard S. Cuckle, Karin Fuchs, Lisa Sullivan, Christine H. Comstock, George R. Saade, Keith Eddleman, Susan Gross, Lorraine Dugoff, Sabrina D. Craigo, Ilan E. Timor-Tritsch, Stephen R. Carr, Honor M. Wolfe, Diana W. Bianchi, Mary E. D’Alton, Role of Second-Trimester Genetic Sonography After Down Syndrome Screening, Obstetrics & Gynecology, 2009, 114, 6, 1189

    CrossRef

  40. 40
    Deborah A Driscoll, Susan J Gross, Screening for fetal aneuploidy and neural tube defects, Genetics in Medicine, 2009, 11, 11, 818

    CrossRef

  41. 41
    Richard C. Cho, Phillip Chu, Rebecca Smith-Bindman, Second trimester prenatal ultrasound for the detection of pregnancies at increased risk of Trisomy 18 based on serum screening, Prenatal Diagnosis, 2009, 29, 2
  42. 42
    J. N. Bottalico, X. Chen, M. Tartaglia, B. Rosario, D. Yarabothu, L. Nelson, Second-trimester genetic sonogram for detection of fetal chromosomal abnormalities in a community-based antenatal testing unit, Ultrasound in Obstetrics & Gynecology, 2009, 33, 2
  43. 43
    D. Cabrol, F. Goffinet, Protocoles cliniques en obstétrique, 2009,

    CrossRef

  44. 44
    Anthony O. Odibo, Harish M. Sehdev, Sabrina Gerkowicz, David M. Stamilio, George A. Macones, Comparison of the efficiency of second-trimester nasal bone hypoplasia and increased nuchal fold in Down syndrome screening, American Journal of Obstetrics and Gynecology, 2008, 199, 3, 281.e1

    CrossRef

  45. 45
    Peter A. Benn, James F. X. Egan, Expected performance of second trimester maternal serum testing followed by a ‘genetic sonogram’ in screening of fetal Down syndrome, Prenatal Diagnosis, 2008, 28, 3
  46. 46
    Sophie Dreux, Camille Olivier, Jean-Michel Dupont, Nathalie Leporrier, Jean-François Oury, Françoise Muller, Maternal serum screening in cases of mosaic and translocation Down syndrome, Prenatal Diagnosis, 2008, 28, 8
  47. 47
    Karen Flood, Fergal D Malone, Screening for fetal abnormalities with ultrasound, Current Opinion in Obstetrics and Gynecology, 2008, 20, 2, 139

    CrossRef

  48. 48
    Michael BETHUNE, Time to reconsider our approach to echogenic intracardiac focus and choroid plexus cysts, Australian and New Zealand Journal of Obstetrics and Gynaecology, 2008, 48, 2
  49. 49
    Peter A. Benn, James F. X. Egan, Second trimester prenatal ultrasound and screening for Down syndrome, Prenatal Diagnosis, 2007, 27, 9
  50. 50
    Howard S. Cuckle, Peter A. Benn, Multi-Marker Maternal Serum Screening for Chromosomal Abnormalities,
  51. 51
    Peter A. Benn, Prenatal Diagnosis of Chromosomal Abnormalities through Amniocentesis,
  52. 52
    Peter A. Benn, Prenatal Diagnosis of Chromosomal Abnormalities through Chorionic Villus Sampling and Amniocentesis,