Prenatal Diagnosis

Cover image for Prenatal Diagnosis

January 1991

Volume 11, Issue 1

Pages fmi–fmi, 1–67

  1. Masthead

    1. Top of page
    2. Masthead
    3. Articles
    4. Short Communications
    1. Masthead (page fmi)

      Article first published online: 21 NOV 2005 | DOI: 10.1002/pd.1970110101

  2. Articles

    1. Top of page
    2. Masthead
    3. Articles
    4. Short Communications
    1. Trisomic pregnancies have normal human chorionic gonadotropin bioactivity (pages 1–6)

      Paul G. Kratzer, Mitchell S. Golbus, David E. Finkelstein and Robert N. Taylor

      Article first published online: 21 NOV 2005 | DOI: 10.1002/pd.1970110102

    2. A revisit of trisomy 20 mosaicism in prenatal diagnosis—an overview of 103 cases (pages 7–15)

      Lillian Y. F. Hsu, Sara Kaffe and Theresa E. Perlis

      Article first published online: 21 NOV 2005 | DOI: 10.1002/pd.1970110103

    3. Prenatal diagnosis of congenital my asthenia with arthrogryposis in a myasthenic mother (pages 17–22)

      Claude Stoll, Marie-Christine Ehret-Mentre, Alain Treisser and Christine Tranchant

      Article first published online: 21 NOV 2005 | DOI: 10.1002/pd.1970110104

    4. Women's choices for fetal chromosome analysis (pages 23–28)

      Lenore Abramsky and C. H. Rodeck

      Article first published online: 21 NOV 2005 | DOI: 10.1002/pd.1970110105

    5. Birth prevalence of down's syndrome in England and Wales (pages 29–34)

      H. Cuckle, K. Nanchahal and N. Wald

      Article first published online: 21 NOV 2005 | DOI: 10.1002/pd.1970110106

    6. Cytogenetic studies of amniotic fluid taken before the 15th week of pregnancy for earlier prenatal diagnosis: A report of 114 consecutive cases (pages 35–40)

      Mr. M. T. Rebello, C. T. H. Gray, D. E. Rooney, J. H. Smith, G. A. Hackett, F. E. Loeffler, D. H. Horwell, R. W. Beard and D. V. Coleman

      Article first published online: 21 NOV 2005 | DOI: 10.1002/pd.1970110107

    7. Extraction of DNA from amniotic fluid cells for the early prenatal diagnosis of genetic disease (pages 41–46)

      Mr. M. T. Rebello, G. Hackett, J. Smith, F. E. Loeffler, S. Robson, N. Maclachlan, R. W. Beard, C. H. Rodeck, R. Williamson, D. V. Coleman and C. Williams

      Article first published online: 21 NOV 2005 | DOI: 10.1002/pd.1970110108

    8. Chorionic villus sampling for fetal karyotyping in missed abortions (pages 55–57)

      Z. Appleman, J. Rosensaft, U. Elchalal, B. Caspi and Dr. J. Chemke

      Article first published online: 21 NOV 2005 | DOI: 10.1002/pd.1970110110

  3. Short Communications

    1. Top of page
    2. Masthead
    3. Articles
    4. Short Communications
    1. A three-year follow-up on a child with low level trisomy 8 mosaicism which was diagnosed prenatally (pages 59–62)

      Lamberto Camurri and Annalisa Chiesi

      Article first published online: 21 NOV 2005 | DOI: 10.1002/pd.1970110111

    2. Identification of duchenne muscular dystrophy genomic probe P20 constant Taq1 fragment corresponding to the EcoRV and Msp1 polymorphisms (pages 63–67)

      N. G. Laing, A. P. Walker, P. A. Akkari, D. C. Chandler, M. G. Layton, M. E. Mears, T. Yamada, R. J. Bartlett, M. A. Pericak-Vance, W.-Y. Hung, M. C. Wapenaar, G. van Ommen, A. D. Roses and B. A. Kakulas

      Article first published online: 21 NOV 2005 | DOI: 10.1002/pd.1970110112

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