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June 1, 1992Journal of Medical GeneticsOpen Access

Terminal 22q deletion associated with a partial deficiency of arylsulphatase A.

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Authors

KNKouji NaraharaYTYoshihiko TakahashiMMMutsumi Murakami

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Cite This Study

Narahara et al. (1992) studied this question.

synapsesocial.com/papers/6a89b6ab176d2ac34cfbb272https://doi.org/10.1136/jmg.29.6.432
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Also Consider

Synapse has enriched 3 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Multiple congenital anomaly/mental retardation (MCA/MR) syndrome with Goldenhar complex due to a terminal del(22q)1988 · 78 citations
  2. 2A familial pericentric inversion of chromosome 22 with a recombinant subject illustrating a 'pure' partial monosomy syndrome.1985 · 84 citations
  3. 3Deleted ring chromosome 22 in a mentally retarded boy1986 · 13 citations