Prenatal Diagnosis

Cover image for Prenatal Diagnosis

May 2002

Volume 22, Issue 5

Pages 345–451

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    1. Pregnancy outcome in fetuses with increased nuchal translucency and normal karyotype (pages 345–349)

      M. V. Senat, B. De Keersmaecker, F. Audibert, G. Montcharmont, R. Frydman and Y. Ville

      Version of Record online: 27 MAR 2002 | DOI: 10.1002/pd.321

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    1. Funipuncture for fetocide in late termination of pregnancy (pages 354–356)

      M. V. Senat, C. Fischer and Y. Ville

      Version of Record online: 27 MAR 2002 | DOI: 10.1002/pd.290

  4. Invited Commentaries

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    1. Prenatal diagnosis in glycogen storage diseases (pages 357–359)

      Yuan-Tsong Chen, Deeksha Bali and Jennifer Sullivan

      Version of Record online: 12 APR 2002 | DOI: 10.1002/pd.166

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    1. Prenatal diagnosis of common aneuploidies using quantitative fluorescent PCR (pages 360–365)

      Chrysanthy Bili, Aspasia Divane, Angela Apessos, Tassis Konstantinos, Athanasiadis Apostolos, Barbarigos Ioannis, Theodoropoulos Periklis and Lina Florentin

      Version of Record online: 18 APR 2002 | DOI: 10.1002/pd.301

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    1. Prenatal diagnosis of brain abnormalities in Wolf–Hirschhorn (4p-) syndrome (pages 366–370)

      B. De Keersmaecker, M. Albert, Y. Hillion and Y. Ville

      Version of Record online: 18 APR 2002 | DOI: 10.1002/pd.318

    2. Prenatal ultrasound diagnosis of frontonasal dysplasia (pages 375–379)

      Pasquale Martinelli, Rosa Russo, Annalisa Agangi and Dario Paladini

      Version of Record online: 27 MAR 2002 | DOI: 10.1002/pd.287

    3. Prenatal diagnosis of a rhodopsin mutation using chemical cleavage of the mismatch (pages 380–384)

      Alessandra Tessitore, Elena Toniato, Alberto Gulino, Luigi Frati, Enrico Ricevuto, Maria Vadalà, Enzo Vingolo and Stefano Martinotti

      Version of Record online: 27 MAR 2002 | DOI: 10.1002/pd.263

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    1. The variation of risk estimates through pregnancy in second trimester maternal serum screening for Down syndrome (pages 385–387)

      Michael Christiansen, Estrid V. Høgdall, Severin O. Larsen and Claus Høgdall

      Version of Record online: 18 APR 2002 | DOI: 10.1002/pd.297

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    1. Prenatal diagnosis of apparently isolated unilateral multicystic kidney: implications for counselling and management (pages 388–394)

      G. Aubertin, S. Cripps, G. Coleman, B. McGillivray, S.L. Yong, M. Van Allen, D. Shaw and L. Arbour

      Version of Record online: 12 APR 2002 | DOI: 10.1002/pd.319

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    1. A case report of prenatally diagnosed ophthalmo-acromelic syndrome type Waardenburg (pages 395–397)

      F. Kara, N. Yesildaglar, R. A. Tuncer, N. Semerci, N. Onat, Y. Ç. Yilmazer, T. Sipahi and S. Erkaya

      Version of Record online: 12 APR 2002 | DOI: 10.1002/pd.331

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    1. Prenatal diagnosis of partial agenesis of the corpus callosum in a fetus with thanatophoric dysplasia type 2 (pages 404–407)

      Karim D. Kalache, Katarina Lehmann, Rabih Chaoui, Dietmar E. Kivelitz, Stefan Mundlos and Rainer Bollmann

      Version of Record online: 12 APR 2002 | DOI: 10.1002/pd.327

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    1. Fetal magnetocardiography: development of the fetal cardiac time intervals (pages 408–414)

      Christiane Kähler, Ekkehard Schleußner, Barbara Grimm, Alina Schneider, Uwe Schneider, Hannes Nowak and Hans J. Seewald

      Version of Record online: 12 APR 2002 | DOI: 10.1002/pd.322

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    1. Prenatal findings in a monozygotic twin pregnancy with Costello syndrome (pages 415–417)

      T. Van den Bosch, D. Van Schoubroeck, J. P. Fryns, G. Naulaers, A. M. Inion and K. Devriendt

      Version of Record online: 12 APR 2002 | DOI: 10.1002/pd.333

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    1. Maternal uniparental isodisomy 10 and mosaicism for an additional marker chromosome derived from the paternal chromosome 10 in a fetus (pages 418–421)

      Monika Schlegel, Alessandra Baumer, Mariluce Riegel, Ute Wiedemann and Albert Schinzel

      Version of Record online: 12 APR 2002 | DOI: 10.1002/pd.337

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    1. First-trimester sonographic diagnosis of distal urethral atresia with megalourethra in VACTERL association (pages 422–424)

      Martin Krapp, Annegret Geipel, Ute Germer, Manuela Krokowski and Ulrich Gembruch

      Version of Record online: 12 APR 2002 | DOI: 10.1002/pd.328

  16. Original Papers

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    1. A simple and effective approach for detecting maternal cell contamination in molecular prenatal diagnosis (pages 425–429)

      T. Antoniadi, C. Yapijakis, P. Kaminopetros, C. Makatsoris, V. Velissariou, D. Vassilopoulos and M. B. Petersen

      Version of Record online: 12 APR 2002 | DOI: 10.1002/pd.325

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    1. Perinatal hepatic infarction in twin–twin transfusion (pages 430–432)

      M. J. O'Sullivan, E. M. Dempsey, W. O. Kirwan and C. A. Ryan

      Version of Record online: 12 APR 2002 | DOI: 10.1002/pd.326

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    1. Isolated sulfite oxidase deficiency: mutation analysis and DNA-based prenatal diagnosis (pages 433–436)

      J. L. Johnson, K. V. Rajagopalan, W. O. Renier, I. Van der Burgt and W. Ruitenbeek

      Version of Record online: 12 APR 2002 | DOI: 10.1002/pd.335

    2. Factors affecting outcomes of prenatally-diagnosed tumours (pages 437–443)

      K. L. Chan, M. H. Y. Tang, H. Y. Tse, R. Y. K. Tang, H. S. W Lam, C. P. Lee and P. K. H. Tam

      Version of Record online: 12 APR 2002 | DOI: 10.1002/pd.324

  19. Current Awareness

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