Clinical Genetics

Cover image for Clinical Genetics

February 1975

Volume 7, Issue 2

Pages 85–180

  1. Original Article

    1. Top of page
    2. Original Article
    1. A possible major contribution to mental retardation in the general population by the gene for microcephaly (pages 85–90)

      Qutub H. Qazi and T. Edward Reed

      Article first published online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1975.tb00302.x

    2. Familial D/D translocation t(13q;14q) Eight members in four generations (pages 91–97)

      Willard R. Centerwall and Preston R. Merrell

      Article first published online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1975.tb00303.x

    3. Incontinentia pigmenti (pages 103–110)

      T. Iancu, L. Komlos, F. Shabtay, E. Elian, I. Halbrecht and J. A. Böök

      Article first published online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1975.tb00305.x

    4. A new form of hereditary short limbed dwarf ism with microcephalus (pages 111–119)

      Richard C. Juberg and Madge B. Van Ness

      Article first published online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1975.tb00306.x

    5. A familial F/G translocation [t(20p-; 22q+)] observed in three generations (pages 120–127)

      Maimon M. Cohen, Ronald G. Davidson and Judith A. Brown

      Article first published online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1975.tb00307.x

    6. Cystic fibrosis heterozygote detection: A study on a normal population (pages 128–133)

      B. Shannon Danes

      Article first published online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1975.tb00308.x

    7. A new case of the trisomy 9p syndrome: Report of a patient with unusual chromosome findings (46,XX/47,XX, + i (9p)) and a peculiar congenital heart defect (pages 134–143)

      E. Orye, H. Verhaaren, H. Van Egmond and A. Devloo-Blancquaert

      Article first published online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1975.tb00309.x

    8. Familial primary vesicoureteral reflux (pages 144–147)

      K. Fried, E. Yuval, A. Eidelman and S. Beer

      Article first published online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1975.tb00310.x

    9. Isochromosome for the short arm of X: A human mosaic 45,X/46,XXpi (pages 148–154)

      P. H. Fitzgerald and R. A. Donald

      Article first published online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1975.tb00311.x

    10. An XX male: Cytogenetic and endocrine studies (pages 155–162)

      Maria E. Rios, Robert L. Kaufman, Gurbax S. Sekhon, James G. Bucy, Joan E. Bauman and Lawrence S. Jacobs

      Article first published online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1975.tb00312.x

    11. Amniotic fluid alphafetoprotein measurements in the early prenatal diagnosis of central nervous system disorders (pages 163–169)

      D. J. H. Brock, I. B. Scrimgeour and M. M. Nelson

      Article first published online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1975.tb00313.x

    12. Alpha fetoprotein levels in maternal serum and in amniotic fluid from early normal pregnancies (pages 170–175)

      B. Nørgaard-Pedersen, J. Lindsten and J. Philip

      Article first published online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1975.tb00314.x

    13. Elevated levels of alfa fetoprotein in maternal serum and amniotic fluid in two cases of spina bifida (pages 176–180)

      E. Malmqvist, J. Lindsten, B. Nørgaard-Pedersen, B. Hellström and B. Sundberg

      Article first published online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1975.tb00315.x

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