ضعف الشم (Arabic Wikipedia)
Analysis of information sources in references of the Wikipedia article "ضعف الشم" in Arabic language version.
doi.org
- 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
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.