ضعف الشم (Arabic Wikipedia)

Analysis of information sources in references of the Wikipedia article "ضعف الشم" in Arabic language version.

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doi.org (Global: 2^nd place; Arabic: 5^th place)

Arkoncel، ML؛ Arkoncel، FR؛ Lantion-Ang، FL (مارس 2011). "A case of Kallmann syndrome". BMJ Case Reports. ج. 2011. DOI:10.1136/bcr.01.2011.3727. PMC:3070321. PMID:22700069. Kallmann syndrome (KS), a rare genetic disorder, refers to the association between hypogonadotropic hypogonadism and anosmia or hyposmia due to abnormal migration of olfactory axons and gonadotropin-releasing hormone producing neurons.

nih.gov (Global: 4^th place; Arabic: 6^th place)

ncbi.nlm.nih.gov

Arkoncel، ML؛ Arkoncel، FR؛ Lantion-Ang، FL (مارس 2011). "A case of Kallmann syndrome". BMJ Case Reports. ج. 2011. DOI:10.1136/bcr.01.2011.3727. PMC:3070321. PMID:22700069. Kallmann syndrome (KS), a rare genetic disorder, refers to the association between hypogonadotropic hypogonadism and anosmia or hyposmia due to abnormal migration of olfactory axons and gonadotropin-releasing hormone producing neurons.

pubmed.ncbi.nlm.nih.gov

Arkoncel، ML؛ Arkoncel، FR؛ Lantion-Ang، FL (مارس 2011). "A case of Kallmann syndrome". BMJ Case Reports. ج. 2011. DOI:10.1136/bcr.01.2011.3727. PMC:3070321. PMID:22700069. Kallmann syndrome (KS), a rare genetic disorder, refers to the association between hypogonadotropic hypogonadism and anosmia or hyposmia due to abnormal migration of olfactory axons and gonadotropin-releasing hormone producing neurons.