Prenatal Diagnosis

Cover image for Prenatal Diagnosis

July 2005

Volume 25, Issue 7

Pages 535–633

  1. Case Reports

    1. Top of page
    2. Case Reports
    3. Short Communications
    4. Original Papers
    5. Short Communications
    6. Original Papers
    7. Case Reports
    8. Original Papers
    9. Letters to the Editor
    10. Current Awareness
    1. Prenatal diagnosis of Bruck syndrome (pages 535–538)

      C. Berg, A. Geipel, F. Noack, J. Smrcek, M. Krapp, U. Germer, G. Bender and U. Gembruch

      Version of Record online: 20 JUL 2005 | DOI: 10.1002/pd.801

    2. Cavum veli interpositi: prenatal diagnosis and postnatal outcome (pages 539–542)

      Prakesh S. Shah, Susan Blaser, Ants Toi, Katherine Fong, Phyllis Glanc, Riyana Babul-Hirji, James Rutka and David Chitayat

      Version of Record online: 20 JUL 2005 | DOI: 10.1002/pd.1114

  2. Short Communications

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

    1. Top of page
    2. Case Reports
    3. Short Communications
    4. Original Papers
    5. Short Communications
    6. Original Papers
    7. Case Reports
    8. Original Papers
    9. Letters to the Editor
    10. Current Awareness
    1. Cardiac time intervals of normal fetuses using noninvasive fetal electrocardiography (pages 546–552)

      Ee Ling Chia, Ting Fei Ho, Mary Rauff and William C. L. Yip

      Version of Record online: 20 JUL 2005 | DOI: 10.1002/pd.1184

    2. Fetal hyperechogenic kidney with normal amniotic fluid volume: a diagnostic dilemma (pages 553–558)

      R. Mashiach, M. Davidovits, B. Eisenstein, D. Kidron, M. Kovo, J. Shalev, P. Merlob, D. Vardimon, Z. Efrat and I. Meizner

      Version of Record online: 20 JUL 2005 | DOI: 10.1002/pd.1185

    3. Rapid detection of fetal aneuploidy using proteomics approaches on amniotic fluid supernatant (pages 559–566)

      Tzu-Hao Wang, Yao-Lung Chang, Hsiu-Huei Peng, Shih-Tien Wang, Hsiao-Wen Lu, Shih-Hua Teng, Shuenn-Dyh Chang and Hsin-Shih Wang

      Version of Record online: 20 JUL 2005 | DOI: 10.1002/pd.1186

    4. Should determination of the karyotype be systematic for all malformations detected by obstetrical ultrasound? (pages 567–573)

      M. Staebler, C. Donner, N. Van Regemorter, L. Duprez, V. De Maertelaer, F. Devreker and F. Avni

      Version of Record online: 20 JUL 2005 | DOI: 10.1002/pd.1187

  4. Short Communications

    1. Top of page
    2. Case Reports
    3. Short Communications
    4. Original Papers
    5. Short Communications
    6. Original Papers
    7. Case Reports
    8. Original Papers
    9. Letters to the Editor
    10. Current Awareness
    1. Prenatal DNA diagnosis of Noonan syndrome in a fetus with massive hygroma colli, pleural effusion and ascites (pages 574–576)

      Gregor Schlüter, Maren Steckel, Holger Schiffmann, Karsten Harms, Volker Viereck, Günter Emons, Peter Burfeind and Hans-Ulrich Pauer

      Version of Record online: 20 JUL 2005 | DOI: 10.1002/pd.1189

  5. Original Papers

    1. Top of page
    2. Case Reports
    3. Short Communications
    4. Original Papers
    5. Short Communications
    6. Original Papers
    7. Case Reports
    8. Original Papers
    9. Letters to the Editor
    10. Current Awareness
    1. Prenatal fetal sex diagnosis by detecting amelogenin gene in maternal plasma (pages 577–581)

      Bin Zhu, Qing-Wen Sun, Ya-Chao Lu, Mao-Ming Sun, Li-Juan Wang and Xing-Hua Huang

      Version of Record online: 20 JUL 2005 | DOI: 10.1002/pd.1192

    2. Precise prenatal diagnosis of tuberous sclerosis by sequencing the TSC2 gene (pages 582–585)

      Aubrey Milunsky, Sung Han Shim, Masamichi Ito, Ronald K. Jaekle, Lori L. Bassett, Michael R. Brumund and Jeff M. Milunsky

      Version of Record online: 20 JUL 2005 | DOI: 10.1002/pd.1197

    3. Educating general practitioners about prenatal testing: approaches and challenges (pages 592–601)

      Sylvia Metcalfe, Michelle Seipolt, MaryAnne Aitken and Anna Flouris

      Version of Record online: 20 JUL 2005 | DOI: 10.1002/pd.1202

  6. Case Reports

    1. Top of page
    2. Case Reports
    3. Short Communications
    4. Original Papers
    5. Short Communications
    6. Original Papers
    7. Case Reports
    8. Original Papers
    9. Letters to the Editor
    10. Current Awareness
    1. Cornelia de Lange Syndrome in association with a balanced reciprocal translocation involving chromosomes 3 and 5 (pages 602–603)

      Natalia Price, Mandeep Bahra, David Griffin, Ghaly Hanna and Anthony Stock

      Version of Record online: 20 JUL 2005 | DOI: 10.1002/pd.1210

  7. Original Papers

    1. Top of page
    2. Case Reports
    3. Short Communications
    4. Original Papers
    5. Short Communications
    6. Original Papers
    7. Case Reports
    8. Original Papers
    9. Letters to the Editor
    10. Current Awareness
    1. Fragmentation of cell-free fetal DNA in plasma and urine of pregnant women (pages 604–607)

      Keiko Koide, Akihiko Sekizawa, Mariko Iwasaki, Ryu Matsuoka, Susumu Honma, Antonio Farina, Hiroshi Saito and Takashi Okai

      Version of Record online: 20 JUL 2005 | DOI: 10.1002/pd.1213

    2. The timing of demise in fetuses with trisomy 21 and trisomy 18 (pages 608–611)

      Rosa H. Won, Robert J. Currier, Fred Lorey and Dena R. Towner

      Version of Record online: 20 JUL 2005 | DOI: 10.1002/pd.1243

  8. Letters to the Editor

    1. Top of page
    2. Case Reports
    3. Short Communications
    4. Original Papers
    5. Short Communications
    6. Original Papers
    7. Case Reports
    8. Original Papers
    9. Letters to the Editor
    10. Current Awareness
    1. Omphalopagus conjoining and twin–twin transfusion syndrome (pages 612–614)

      J. C. Y. Chan, D. A. Somerset, N. Ostojic, P. Cox, P. Young, L. Brueton and M. D. Kilby

      Version of Record online: 20 JUL 2005 | DOI: 10.1002/pd.824

    2. The importance of investigating an apparently simple Yq deletion detected prenatally (pages 614–616)

      Mary Ann Thomas, Valerie Desilets, F. Halal and Alessandra M. V. Duncan

      Version of Record online: 20 JUL 2005 | DOI: 10.1002/pd.1117

    3. Prenatal diagnosis of an acardiac amorphous twin and the anomalous co-twin in a monoamniotic twin pregnancy (pages 618–620)

      Chih-Ping Chen, Jin-Chung Shih, Tung-Yao Chang, Schu-Rern Chern, Ching-Yi Lin, Wayseen Wang and Chin-Yuan Tzen

      Version of Record online: 20 JUL 2005 | DOI: 10.1002/pd.1174

    4. A novel pericentric inversion of chromosome 14 involving the rRNA gene cluster (pages 620–621)

      Natalia T Leach, Suzanne M Cole, Deborah J Sandstrom and Stanislawa Weremowicz

      Version of Record online: 20 JUL 2005 | DOI: 10.1002/pd.1200

    5. Prenatal diagnosis of cranial vault defects (page 627)

      S. Bianca, G. Bartoloni, C. Tetto, B. Pirruccello, C. Ingegnosi, A. Cataliotti and G. Ettore

      Version of Record online: 20 JUL 2005 | DOI: 10.1002/pd.1190

  9. Current Awareness

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

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