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pro vyhledávání: '"Değirmenci, Banu"'
Autor:
Değirmenci, Banu, Solak, Mustafa, Yildiz, Saliha Handan, Erdogan, Müjgan Ozdemir, Elmas, Muhsin, Fistik, Tevhide
Publikováno v:
In Meta Gene February 2019 19:78-81
Additional file 1:. CARE Checklist of information to include when writing a case report
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::17d46c14f525a38aaa31a6481db9df64
Pentazomi X hipotonisite, gelişme geriliği, orta dereceden ağır dereceye kadar zeka geriliği, kısa boy, kraniofasiyal anomaliler ve kas-iskelet sistemi bozuklukları ile karakterize nadir görülen bir cinsiyet kromozom anöploidi bozukluğudur
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______9458::e49ebc90921e40d1d83322b69a549178
http://hdl.handle.net/11452/19287
http://hdl.handle.net/11452/19287
Publikováno v:
Volume: 40, Issue: 3 157-159
Uludağ Üniversitesi Tıp Fakültesi Dergisi
Uludağ Üniversitesi Tıp Fakültesi Dergisi
Pentasomy X is a rare sex chromosomal aneuploidy disorder characterized by hypotonia, developmental delay, moderate to severe mental retardation, short stature, craniofacial anomalies and musculoskeletal abnormalities. The craniofacial anomalies may
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=tubitakulakb::7161a6361d84d5a8ab8fb720db99f999
https://dergipark.org.tr/tr/pub/uutfd/issue/35301/391847
https://dergipark.org.tr/tr/pub/uutfd/issue/35301/391847
Autor:
Elmas, Muhsin1 (AUTHOR) drmelmas@gmail.com, Gogus, Basak1 (AUTHOR), Değirmenci, Banu2 (AUTHOR), Solak, Mustafa1 (AUTHOR), Gleeson, J. G.3,4 (AUTHOR)
Publikováno v:
Egyptian Journal of Medical Human Genetics. 7/15/2020, Vol. 21 Issue 1, p1-5. 5p.