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There are 2635078 results for: content related to: Otodental dysplasia: a “new” ectodermal dysplasia

  1. Increased “reproductive casualty” in heterozygotes for phenylketonuria

    Clinical Genetics

    Volume 4, Issue 2, March 1973, Pages: 105–114, L. Fegersten Saugstad

    Article first published online : 23 APR 2008, DOI: 10.1111/j.1399-0004.1973.tb01130.x

  2. Neuraminidase deficiency in the original patient with the Goldberg Syndrome

    Clinical Genetics

    Volume 16, Issue 5, November 1979, Pages: 323–330, George H. Thomas, Morton F. Goldberg, Carol S. Miller and Linda W. Reynolds

    Article first published online : 23 APR 2008, DOI: 10.1111/j.1399-0004.1979.tb01010.x

  3. Chromosomal anomalies in patients with retinoblastoma

    Clinical Genetics

    Volume 12, Issue 1, July 1977, Pages: 1–8, Miriam G. Wilson, Allan J. Ebbin, Joseph W. Towner and William H. Spencer

    Article first published online : 23 APR 2008, DOI: 10.1111/j.1399-0004.1977.tb00894.x

  4. Bloom's syndrome. V. Surveillance for cancer in affected families

    Clinical Genetics

    Volume 12, Issue 3, September 1977, Pages: 162–168, James German, David Bloom and Eberhard Passarge

    Article first published online : 23 APR 2008, DOI: 10.1111/j.1399-0004.1977.tb00919.x

  5. Bisatellited extra small metacentric chromosome in newborns

    Clinical Genetics

    Volume 6, Issue 1, July 1974, Pages: 23–31, Ursula Friedrich and Johannes Nielsen

    Article first published online : 23 APR 2008, DOI: 10.1111/j.1399-0004.1974.tb00626.x

  6. Altered isoenzyme patterns of liver α-L-fucosidase in cystic fibrosis

    Clinical Genetics

    Volume 10, Issue 2, August 1976, Pages: 63–72, Jack A. Alhadeff, Linda Tennant and John S. O'Brien

    Article first published online : 23 APR 2008, DOI: 10.1111/j.1399-0004.1976.tb00014.x

  7. Menkes Kinky Hair Syndrome: Is it a treatable disorder?

    Clinical Genetics

    Volume 11, Issue 2, February 1977, Pages: 154–161, A. D. Garnica, J. L. Frias and O. M. Rennert

    Article first published online : 23 APR 2008, DOI: 10.1111/j.1399-0004.1977.tb01294.x

  8. Catecholamine metabolism in familial amyloid polyneuropathy

    Clinical Genetics

    Volume 16, Issue 2, August 1979, Pages: 117–124, Tomokazu Suzuki, Isao Tsuge, Sadayoshi Higa, Akira Hayashi, Yuichi Yamamura, Yoshio Takaba and Akira Nakajima

    Article first published online : 23 APR 2008, DOI: 10.1111/j.1399-0004.1979.tb00860.x

  9. Confirmation of an influence of the inherited Lp(a) variation on serum insulin and glucose levels

    Clinical Genetics

    Volume 16, Issue 6, December 1979, Pages: 418–427, Gösta Dahléni and Kare Berg

    Article first published online : 23 APR 2008, DOI: 10.1111/j.1399-0004.1979.tb01350.x

  10. Adult-onset hereditary cerebellar ataxia and neurosensory deafness

    Clinical Genetics

    Volume 6, Issue 5, November 1974, Pages: 416–421, R. Neil Schimke

    Article first published online : 28 JUN 2008, DOI: 10.1111/j.1399-0004.1974.tb02265.x

  11. High frequency of atypical pseudocholinesterase gene among Iraqi and Iranian Jews*

    Clinical Genetics

    Volume 3, Issue 2, March 1972, Pages: 123–127, A. Szeinberg, S. Pipano, M. Assa, J. H. Medalie and H. N. Neufeld

    Article first published online : 23 APR 2008, DOI: 10.1111/j.1399-0004.1972.tb01733.x

  12. Amino acid composition of the serum low density lipoprotein in patients with familial lecithin:cholesterol acyltransferase deficiency

    Clinical Genetics

    Volume 1, Issue 5-6, November 1970, Pages: 349–352, Helge Boman and Harald Torsvik

    Article first published online : 28 JUN 2008, DOI: 10.1111/j.1399-0004.1970.tb02253.x

  13. Are 1q+ chromosomes harmless?

    Clinical Genetics

    Volume 6, Issue 5, November 1974, Pages: 383–393, R. J. M. Gardner, Helen R. McCreanor, M. I. Parslow and A. M. O. Veale

    Article first published online : 28 JUN 2008, DOI: 10.1111/j.1399-0004.1974.tb02261.x

  14. An atypical case of Cockayne's syndrome

    Clinical Genetics

    Volume 4, Issue 1, January 1973, Pages: 28–32, R. A. Pfeiffer and K. D. Bachmann

    Article first published online : 23 APR 2008, DOI: 10.1111/j.1399-0004.1973.tb01118.x

  15. Histidinuria: A renal and intestinal histidine transport deficiency found in two mentally retarded children

    Clinical Genetics

    Volume 9, Issue 2, February 1976, Pages: 117–124, Juan Sabater, Carmen Ferré, Maria Puliol and Antonio Maya

    Article first published online : 23 APR 2008, DOI: 10.1111/j.1399-0004.1976.tb01556.x

  16. On the classification of the acrocephalosyndactyly syndromes

    Clinical Genetics

    Volume 12, Issue 3, September 1977, Pages: 169–178, Victor Escobar and David Bixler

    Article first published online : 23 APR 2008, DOI: 10.1111/j.1399-0004.1977.tb00920.x

  17. Dermatoglyphics in Cri du Chat syndrome

    Clinical Genetics

    Volume 11, Issue 2, February 1977, Pages: 214–218, Hiroshi Shiono, Jun-Ichi Kadowaki and Hisashi Kazama

    Article first published online : 23 APR 2008, DOI: 10.1111/j.1399-0004.1977.tb01302.x

  18. Friedreich's ataxia in Western Norway

    Clinical Genetics

    Volume 7, Issue 4, April 1975, Pages: 287–298, Håvard Skre

    Article first published online : 23 APR 2008, DOI: 10.1111/j.1399-0004.1975.tb00331.x

  19. Autosomal monosomy (45, XX, C—) in a humanembryo with total amelia and further malformations

    Clinical Genetics

    Volume 4, Issue 3, May 1973, Pages: 193–202, I. H. Pawlowitzki, A. Cenani and H. J. Frischbier

    Article first published online : 23 APR 2008, DOI: 10.1111/j.1399-0004.1973.tb01142.x

  20. The human X-chromosome and the levels of serum immunoglobulin M

    Clinical Genetics

    Volume 15, Issue 3, March 1979, Pages: 221–227, Victor Escobar, Linda A. Corey, David Bixler, Walter E. Nance and Angenieta Biegei

    Article first published online : 23 APR 2008, DOI: 10.1111/j.1399-0004.1979.tb00971.x