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September 1, 1987American Journal of Medical Genetics

Clinical heterogeneity associated with deletions in the long arm of chromosome 15: Report of 3 new cases and their possible genetic significance

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Authors

LKLawrence C. KaplanYale UniversityRWRobert H. WhartonBoston Children's HospitalEEEllen Roy EliasChildren's Hospital Colorado

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Cite This Study

Kaplan et al. (1987) studied this question.

synapsesocial.com/papers/6a6fc5d9f44fa9f079dd4372https://doi.org/10.1002/ajmg.1320280107
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Also Consider

Synapse has enriched 4 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Angelman's ("Happy Puppet") Syndrome1972 · 43 citations
  2. 2Duplication in chromosome 15q in a boy with the Prader‐Willi syndrome; further cytogenetic confusion1984 · 29 citations
  3. 3Isolation of molecular probes associated with the chromosome 15 instability in the Prader-Willi syndrome.1986 · 159 citations
  4. 4Deletion of chromosome 15 (q11 – 13) in a Prader‐Labhart‐Willi syndrome clinic population1984 · 52 citations