Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Zahra Kamel Koleti"'
Publikováno v:
Archives of Medical Science, Vol 13, Iss 1, Pp 215-220 (2016)
Noonan syndrome (NS) is an autosomal dominant disorder with vast heterogeneity in clinical and genetic features. Various symptoms have been reported for this abnormality such as short stature, unusual facial characteristics, congenital heart abnormal
Externí odkaz:
https://doaj.org/article/64b6ee2425fd4f2888f0f8d9cfc09066
Publikováno v:
Genes
Genes, Vol 12, Iss 361, p 361 (2021)
Genes, Vol 12, Iss 361, p 361 (2021)
Direct-to-consumer genetic tests (DTC-GT) have become a bridge between marketing and traditional healthcare services. After earning FDA endorsement for such facilities, several fast-developing companies started to compete in the related area. Pharmac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0b86ae4e14438e3b3b18021801ef2537
http://europepmc.org/articles/PMC7999840
http://europepmc.org/articles/PMC7999840
Publikováno v:
Archives of Medical Science, Vol 13, Iss 1, Pp 215-220 (2016)
Archives of Medical Science : AMS
Archives of Medical Science : AMS
Noonan syndrome (NS) is an autosomal dominant disorder with vast heterogeneity in clinical and genetic features. Various symptoms have been reported for this abnormality such as short stature, unusual facial characteristics, congenital heart abnormal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::de46d4fb8983536ce4d5cc0e7453d9ec
https://doi.org/10.5114/aoms.2017.64720
https://doi.org/10.5114/aoms.2017.64720
Autor:
Tafazoli, Alireza1, Eshraghi, Peyman2, Koleti, Zahra Kamel3, Abbaszadegan, Mohammadreza4 Abbaszadeganmr@mums.ac.ir
Publikováno v:
Archives of Medical Science. 2017, Vol. 13 Issue 1, p215-222. 8p.
Autor:
Tafazoli, Alireza, Guggilla, Rama Krishna, Kamel-Koleti, Zahra, Miltyk, Wojciech, Gervasini, Guillermo, Caruz, Caruz
Publikováno v:
Genes; Mar2021, Vol. 12 Issue 3, p361-361, 1p