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Talk:Barakat syndrome

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Resources

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The following case studies may be useful:

  • Ranjbar-Omrani, G (2008 May). "Concomitant hypoparathyroidism, sensorineural deafness, and renal agenesis: a case of Barakat syndrome". Archives of Iranian medicine. 11 (3): 337–40. doi:08113/AIM.0019. PMID 18426329. {{cite journal}}: Check |doi= value (help); Check date values in: |date= (help); Unknown parameter |coauthors= ignored (|author= suggested) (help)
  • Chatterjee, Atri (1 January 2013). "Seizure, deafness and renal agenesis: A rare case of barakat syndrome". Annals of Indian Academy of Neurology. 16 (1): 91. doi:10.4103/0972-2327.107707. PMC 3644792. PMID 23661972. {{cite journal}}: Unknown parameter |coauthors= ignored (|author= suggested) (help)CS1 maint: unflagged free DOI (link)

DiptanshuTalk 21:09, 14 September 2013 (UTC)[reply]

Article copying from wikipedia

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FYI, this paper copies from this article rather than the other way around. I think there is a talkpage template for informing people of this, but I couldn't find what it was called. The Syndrome of Familial Hypoparathyroidism, Sensorineural Deafness and Renal Dysplasia Natureium (talk) 02:16, 18 September 2018 (UTC)[reply]