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Terminal long-arm deletion of chromosome 1 in a male infant

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Summary

The clinical findings in a child with a terminal deletion (1) (q42»qter) is described and compared with three cses with a similar chromosomal anomaly.

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Authors and Affiliations

  1. The Mental Retardation Research Center, Institute for Developmental Research, Children's Hospital Research Foundation, 45229, Cincinnati, Ohio, USA

    P. J. Dignan & Shirley Soukup

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  1. P. J. Dignan
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  2. Shirley Soukup
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Dignan, P.J., Soukup, S. Terminal long-arm deletion of chromosome 1 in a male infant. Hum Genet 48, 151–156 (1979). https://doi.org/10.1007/BF00286898

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  • DOI: https://doi.org/10.1007/BF00286898

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