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June 12, 2012Human Mutation

Molecular characterization of Joubert syndrome in Saudi Arabia

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Authors

AAAnas M. AlazamiKing Faisal Specialist Hospital & Research CentreMAMuneera AlshammariKing Saud Medical CityMSMustafa A. SalihKing Abdulaziz City for Science and Technology

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Alazami et al. (2012) studied this question.

synapsesocial.com/papers/6a74408073ed22dccea7f97bhttps://doi.org/10.1002/humu.22134
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Also Consider

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

  1. 1Clinical and molecular characterisation of Bardet–Biedl syndrome in consanguineous populations: the power of homozygosity mapping2009 · 87 citations
  2. 2Joubert Syndrome: Episodic Hyperpnea, Abnormal Eye Movements, Retardation and Ataxia, Associated with Dysplasia of the Cerebellar Vermis1977 · 167 citations
  3. 3Clinical Features and Revised Diagnostic Criteria in Joubert Syndrome1999 · 252 citations