Interstitial deletion of chromosome 13 and associated congenital anomalies

Warren W. Nichols, Robert C. Miller, Elizabeth Hoffman, Daniel Albert, Ralph R. Weichselbaum, John Nove, John B. Little

Research output: Contribution to journalArticle

20 Scopus citations

Abstract

An interstitial deletion of chromosome 13 with breakpoints at 13q22 and 13q32 is presented. The clinical findings associated with this deletion are discussed in relation to the correlations of specific chromosomal bands with constellations of congenital defects as described by Niebuhr and Ottosen (1973), Niebuhr (1977), Lewandowski and Yunis (1975), and Noel et al. (1976).

Original languageEnglish (US)
Pages (from-to)169-173
Number of pages5
JournalHuman genetics
Volume52
Issue number2
DOIs
StatePublished - Nov 1 1979

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

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    Nichols, W. W., Miller, R. C., Hoffman, E., Albert, D., Weichselbaum, R. R., Nove, J., & Little, J. B. (1979). Interstitial deletion of chromosome 13 and associated congenital anomalies. Human genetics, 52(2), 169-173. https://doi.org/10.1007/BF00271569