Σύνδρομο Οκαμότο (Greek Wikipedia)

Analysis of information sources in references of the Wikipedia article "Σύνδρομο Οκαμότο" in Greek language version.

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1web.archive.org

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doi.org

dx.doi.org

Au, P.Y. Billie; You, Jing; Caluseriu, Oana; Schwartzentruber, Jeremy; Majewski, Jacek; Bernier, Francois P.; Ferguson, Marcia; Valle, David και άλλοι. (October 2015). «GeneMatcher Aids in the Identification of a New Malformation Syndrome with Intellectual Disability, Unique Facial Dysmorphisms, and Skeletal and Connective Tissue Abnormalities Caused by De Novo Variants in HNRNPK». Human Mutation 36 (10): 1009–1014. doi:10.1002/humu.22837. ISSN 1059-7794. PMID 26173930.

ethnos.gr

https://www.ethnos.gr/ellada/78991_minyma-elpidas-apo-tin-16hroni-marilena-poy-pashei-apo-syndromo-okamoto

i-diadromi.gr

http://www.i-diadromi.gr/2019/02/syndrome-okamoto.html

iatropedia.gr

https://www.iatropedia.gr/ygeia/ti-ine-to-sindromo-okamoto/31268/

nih.gov

ncbi.nlm.nih.gov

Au, Ping-Yee Billie; Innes, A. Micheil; Kline, Antonie D. (2019), Adam, Margaret P.; Ardinger, Holly H.; Pagon, Roberta A. και άλλοι, επιμ., Au-Kline Syndrome, University of Washington, Seattle, PMID 30998304, http://www.ncbi.nlm.nih.gov/books/NBK540283/, ανακτήθηκε στις 2019-12-02
Au, P.Y. Billie; You, Jing; Caluseriu, Oana; Schwartzentruber, Jeremy; Majewski, Jacek; Bernier, Francois P.; Ferguson, Marcia; Valle, David και άλλοι. (October 2015). «GeneMatcher Aids in the Identification of a New Malformation Syndrome with Intellectual Disability, Unique Facial Dysmorphisms, and Skeletal and Connective Tissue Abnormalities Caused by De Novo Variants in HNRNPK». Human Mutation 36 (10): 1009–1014. doi:10.1002/humu.22837. ISSN 1059-7794. PMID 26173930.

rarediseases.info.nih.gov

https://rarediseases.info.nih.gov/diseases/4064/okamoto-syndrome

pubmedcentral.nih.gov

Au, P.Y. Billie; You, Jing; Caluseriu, Oana; Schwartzentruber, Jeremy; Majewski, Jacek; Bernier, Francois P.; Ferguson, Marcia; Valle, David και άλλοι. (October 2015). «GeneMatcher Aids in the Identification of a New Malformation Syndrome with Intellectual Disability, Unique Facial Dysmorphisms, and Skeletal and Connective Tissue Abnormalities Caused by De Novo Variants in HNRNPK». Human Mutation 36 (10): 1009–1014. doi:10.1002/humu.22837. ISSN 1059-7794. PMID 26173930.

orpha.net

«Orphanet: Okamoto syndrome». www.orpha.net (στα Αγγλικά). Αρχειοθετήθηκε από το πρωτότυπο στις 26 Νοεμβρίου 2020. Ανακτήθηκε στις 30 Νοεμβρίου 2019.

web.archive.org

«Orphanet: Okamoto syndrome». www.orpha.net (στα Αγγλικά). Αρχειοθετήθηκε από το πρωτότυπο στις 26 Νοεμβρίου 2020. Ανακτήθηκε στις 30 Νοεμβρίου 2019.

worldcat.org

Au, P.Y. Billie; You, Jing; Caluseriu, Oana; Schwartzentruber, Jeremy; Majewski, Jacek; Bernier, Francois P.; Ferguson, Marcia; Valle, David και άλλοι. (October 2015). «GeneMatcher Aids in the Identification of a New Malformation Syndrome with Intellectual Disability, Unique Facial Dysmorphisms, and Skeletal and Connective Tissue Abnormalities Caused by De Novo Variants in HNRNPK». Human Mutation 36 (10): 1009–1014. doi:10.1002/humu.22837. ISSN 1059-7794. PMID 26173930.