Summary
Clinical, dermatoglyphic and cytogenetic features of a child with apparently balanced karyotype carrying a presumptive 2/E translocation are presented. The relevance of the karyotypic anomaly to the clinical findings is briefly discussed.
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Masterson, J., Law, E., MacDonald, A. et al. Congenital abnormalities in a child with presumptive karyotype 46. XX, t (2q−; 17q+). I. J. Med. Sc. 3, 1–4 (1970). https://doi.org/10.1007/BF02958727
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DOI: https://doi.org/10.1007/BF02958727