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August 1, 1985Journal of Medical GeneticsOpen Access

A familial pericentric inversion of chromosome 22 with a recombinant subject illustrating a 'pure' partial monosomy syndrome.

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Authors

JWJ L WattUniversity of AberdeenIOI. A. OlsonUniversity of PittsburghAJA W JohnstonChesterfield Royal Hospital NHS Foundation Trust

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Cite This Study

Watt et al. (1985) studied this question.

synapsesocial.com/papers/6a89b6ab176d2ac34cfbb274https://doi.org/10.1136/jmg.22.4.283
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Also Consider

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

  1. 1Phenotypic correlations in patients with ring chromosome 221977 · 48 citations
  2. 2Trisomy 22. Two new cases and delineation of the phenotype.1975 · 31 citations
  3. 3Familial translocation with partial trisomy of 13 and 22: evidence that specific regions of chromosomes 13 and 22 are responsible for the phenotype of each trisomy.1977 · 27 citations
  4. 4Phenotypic variation in two patients with a ring chromosome 221979 · 21 citations