Prenatal Diagnosis

Cover image for Prenatal Diagnosis

November 2005

Volume 25, Issue 11

Pages 977–1078

  1. Original Papers

    1. Top of page
    2. Original Papers
    3. Short Communications
    4. Original Papers
    5. Short Communications
    6. Case Reports
    7. Original Papers
    8. Case Reports
    9. Letters to the Editor
    10. Current Awareness
    1. Population screening for fetal trisomy 21: easy access to screening should be balanced against a uniform ultrasound protocol (pages 984–990)

      Wilfried J. A. Gyselaers, Annie J. Vereecken, Erik J. H. Van Herck, Dany P. L. Straetmans, Eric T. M. de Jonge, Willem U. A. M. Ombelet and Jan G. Nijhuis

      Version of Record online: 20 OCT 2005 | DOI: 10.1002/pd.1217

  2. Short Communications

    1. Top of page
    2. Original Papers
    3. Short Communications
    4. Original Papers
    5. Short Communications
    6. Case Reports
    7. Original Papers
    8. Case Reports
    9. Letters to the Editor
    10. Current Awareness
    1. Gorlin syndrome presenting as prenatal chylothorax in a girl (pages 997–999)

      D. Geneviève, E. Walter, P. Gorry, M. L. Jacquemont, L. Dupic, V. Layet, A. Munnich, V. Cormier-Daire, M. Dommergues, S. Lyonnet and D. Mitanchez

      Version of Record online: 17 OCT 2005 | DOI: 10.1002/pd.1231

  3. Original Papers

    1. Top of page
    2. Original Papers
    3. Short Communications
    4. Original Papers
    5. Short Communications
    6. Case Reports
    7. Original Papers
    8. Case Reports
    9. Letters to the Editor
    10. Current Awareness
  4. Short Communications

    1. Top of page
    2. Original Papers
    3. Short Communications
    4. Original Papers
    5. Short Communications
    6. Case Reports
    7. Original Papers
    8. Case Reports
    9. Letters to the Editor
    10. Current Awareness
    1. Is there an increased rate of anencephaly in twins? (pages 1007–1010)

      Ido Ben-Ami, Zvika Vaknin, Orit Reish, Dan Sherman, Arie Herman and Ron Maymon

      Version of Record online: 17 OCT 2005 | DOI: 10.1002/pd.1233

    2. Detection of a novel dystrophin gene mutation through carrier analysis performed during prenatal diagnosis in a case with intragenic recombination (pages 1011–1014)

      Antonio Percesepe, Maurizio Ferrari, Domenico Coviello, Monica Zanussi, Marina Castagni, Isabella Neri, Maurizio Travi, Antonino Forabosco and Silvana Tedeschi

      Version of Record online: 17 OCT 2005 | DOI: 10.1002/pd.1238

    3. Hydrops fetalis: an unusual prenatal presentation of hereditary congenital lymphedema (pages 1015–1018)

      Etty Daniel-Spiegel, Arash Ghalamkarpour, Ronen Spiegel, Ehud Weiner, Miikka Vikkula, Eliezer Shalev and Stavit Alon Shalev

      Version of Record online: 17 OCT 2005 | DOI: 10.1002/pd.1237

  5. Case Reports

    1. Top of page
    2. Original Papers
    3. Short Communications
    4. Original Papers
    5. Short Communications
    6. Case Reports
    7. Original Papers
    8. Case Reports
    9. Letters to the Editor
    10. Current Awareness
    1. Early ultrasonographic changes in Fowler syndrome features and review of the literature (pages 1019–1023)

      Ihab M. Usta, Antoine A. AbuMusa, Nabil G. Khoury and Anwar H. Nassar

      Version of Record online: 17 OCT 2005 | DOI: 10.1002/pd.1240

    2. Prenatal diagnosis of jumping translocation involving chromosome 22 with ultrasonographic findings (pages 1024–1027)

      Halil Aslan, Birsen Karaman, Gokhan Yildirim and Yavuz Ceylan

      Version of Record online: 17 OCT 2005 | DOI: 10.1002/pd.1241

  6. Original Papers

    1. Top of page
    2. Original Papers
    3. Short Communications
    4. Original Papers
    5. Short Communications
    6. Case Reports
    7. Original Papers
    8. Case Reports
    9. Letters to the Editor
    10. Current Awareness
    1. TORCH test for fetal medicine indications: only CMV is necessary in the United Kingdom (pages 1028–1031)

      Sherif A. Abdel-Fattah, Abha Bhat, Sebastian Illanes, Jose L. Bartha and David Carrington

      Version of Record online: 17 OCT 2005 | DOI: 10.1002/pd.1242

    2. Rapid detection of chromosomal aneuploidies in uncultured amniocytes by multiplex ligation-dependent probe amplification (MLPA) (pages 1032–1039)

      R. Hochstenbach, J. Meijer, J. van de Brug, I. Vossebeld-Hoff, R. Jansen, R. B. van der Luijt, R. J. Sinke, G. C. M. L. Page-Christiaens, J.-K. Ploos van Amstel and J. M. de Pater

      Version of Record online: 17 OCT 2005 | DOI: 10.1002/pd.1247

    3. Reliable test for prenatal prediction of fetal RhD type using maternal plasma from RhD negative women (pages 1040–1044)

      Frederik Banch Clausen, Grethe Risum Krog, Klaus Rieneck, Leif Kofoed Nielsen, Rasmus Lundquist, Kirstin Finning, Ebbe Dickmeiss, Morten Hedegaard and Morten Hanefeld Dziegiel

      Version of Record online: 17 OCT 2005 | DOI: 10.1002/pd.1248

  7. Case Reports

    1. Top of page
    2. Original Papers
    3. Short Communications
    4. Original Papers
    5. Short Communications
    6. Case Reports
    7. Original Papers
    8. Case Reports
    9. Letters to the Editor
    10. Current Awareness
  8. Letters to the Editor

    1. Top of page
    2. Original Papers
    3. Short Communications
    4. Original Papers
    5. Short Communications
    6. Case Reports
    7. Original Papers
    8. Case Reports
    9. Letters to the Editor
    10. Current Awareness
    1. Sonographic diagnosis of fetal adrenal hyperplasia: utility for prenatal corticotherapy (pages 1060–1061)

      Marie Cassart, Anne Massez, Catherine Donner, Claudine Heinrichs and Freddy Avni

      Version of Record online: 21 NOV 2005 | DOI: 10.1002/pd.1219

    2. Three-dimensional ultrasound of dicephalus conjoined twins at 9 weeks of gestation (pages 1063–1064)

      Nobuhiro Suzumori, Tamao Nakanishi, Saori Kaneko, Tamao Yamamoto, Mitsuyo Tanemura, Yoshikatsu Suzuki and Kaoru Suzumori

      Version of Record online: 21 NOV 2005 | DOI: 10.1002/pd.1283

    3. Congenital pulmonary myofibroblastic tumor—pathology and prenatal sonographic appearance (pages 1064–1066)

      Ari Reiss, Yael Goldberg, Mariana Monichor and Arie Drugan

      Version of Record online: 21 NOV 2005 | DOI: 10.1002/pd.1293

    4. Prenatal diagnosis of low-level mosaic trisomy 7 by amniocentesis (pages 1067–1069)

      Chih-Ping Chen, Schu-Rern Chern, Li-Feng Chen, Wen-Lin Chen and Wayseen Wang

      Version of Record online: 21 NOV 2005 | DOI: 10.1002/pd.1297

    5. Prenatal diagnosis of partial trisomy 10q (10q25.3[RIGHTWARDS ARROW]qter) and partial monosomy 18q (18q23[RIGHTWARDS ARROW]qter) (pages 1069–1071)

      Chih-Ping Chen, Schu-Rern Chern, Tung-Yao Chang, Chen-Chi Lee, Wen-Lin Chen and Wayseen Wang

      Version of Record online: 21 NOV 2005 | DOI: 10.1002/pd.1298

  9. Current Awareness

    1. Top of page
    2. Original Papers
    3. Short Communications
    4. Original Papers
    5. Short Communications
    6. Case Reports
    7. Original Papers
    8. Case Reports
    9. Letters to the Editor
    10. Current Awareness

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