Search Within

Stephanie Sherman

Formats
  1. Journal Article (8)
  2. Conference Paper (4)
  3. Meeting Abstract (3)
People
  1. Newton Morton (2)
  2. Andre Rogatko (1)
  3. Danny Wu (1)
Years
  1. 1989 (1)
  2. 1988 (5)
  3. 1987 (4)
  4. 1986 (5)
Publications
  1. Genetic Epidemiology (5)
  2. American Journal of Medical Genetics (4)
  3. Cytogenetics and Cell Genetics (3)
  4. American Journal of Human Genetics (2)
  5. Human Genetics (1)
Publishers
  1. John Wiley & Sons, Inc. (4)
  2. Wiley Liss (4)
  3. S. Karger AG (3)
  4. Cell Press (2)
  5. John Wiley & Sons (1)
  6. Springer (1)

Results (15)

Export to EndNote / Excel | PubMed

Citation style sort is year ascending, and then by author or title. Author ascending is default.
  • Combined segregation and linkage analysis for IDDM and HLA‐DR under several ascertainment assumptions
    Journal Article

    Pascoe, L.; Sherman, S.; Wu, D.; Becker, M.; Falk, C.
    Genetic Epidemiology (1989)

    Fulltext@MSK | Save
  • A segregation and linkage study of classical and nonclassical 21-hydroxylase deficiency
    Journal Article

    Sherman, S. L.; Aston, C. E.; Morton, N. E.; Speiser, P. W.; New, M. I.
    American Journal of Human Genetics (1988)

    Fulltext@MSK | Save
  • Recurrence risks for relatives in families with an isolated case of the fragile X syndrome
    Journal Article

    Sherman, S. L.; Rogatko, A.; Turner, G.
    American Journal of Medical Genetics (1988)

    Fulltext@MSK | Save
  • Investigation of the twinning rate in families with the fragile X syndrome
    Journal Article

    Sherman, S. L.; Turner, G.; Sheffield, L.; Laing, S.; Robinson, H.
    American Journal of Medical Genetics (1988)

    Fulltext@MSK | Save
  • Genetic mapping of the 21-hydroxylase locus: Estimation of small recombination frequencies
    Journal Article

    Aston, C. E.; Sherman, S. L.; Morton, N. E.; Speiser, P. W.; New, M. I.
    American Journal of Human Genetics (1988)

    Fulltext@MSK | Save
  • Investigation of the segregation of the fragile X mutation in daughters of obligate carrier women
    Journal Article

    Sherman, S. L.; Turner, G.; Robinson, H.; Laing, S.
    American Journal of Medical Genetics (1988)

    Fulltext@MSK | Save
  • Comparison of orders involving Fy among physically located chromosome-1 markers
    Meeting Abstract

    Sherman, S. L.; Lewis, M.; McAlpine, P. J.; King, J.
    Cytogenetics and Cell Genetics (1987)

    Fulltext@MSK | Save
  • Linkage studies in myotonic dystrophy and chromosome 19 markers
    Meeting Abstract

    Pericak-Vance, M. A.; Bartlett, R. J.; Yamaoka, L. H.; Haynes, C.; Sherman, S. L.; Thibault, M. C.; Wieringa, B.; Laberge, C.; Ropers, H. H.; Schneider, S.; more...
    Cytogenetics and Cell Genetics (1987)

    Fulltext@MSK | Save
  • Reevaluation of the lod scores involving JK and CO to the chromosome 2 markers of IGK and ACP1
    Meeting Abstract

    Keats, B. J. B.; Falk, C. T.; Sherman, S. L.
    Cytogenetics and Cell Genetics (1987)

    Fulltext@MSK | Save
  • Hypothesis regarding the nature of the fragile X mutation: A reply to Winter and Pembrey
    Journal Article

    Brown, W. T.; Sherman, S. L.; Dobkin, C. S.
    Human Genetics (1987)

    Fulltext@MSK | Save