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of 6
pro vyhledávání: '"Sultana, Faradz"'
Autor:
Fatinah Shahab, Tania Tedjo Minuljo, Calvin Layuk Allo, Dody Priambada, Mahayu Dewi Ariani, Sultana Faradz
Publikováno v:
Acta Medica Indonesiana, Vol 55, Iss 1 (2023)
Macroadenoma is a tumor that typically develops in the epithelial cells of the pituitary gland. Patients suffering from the condition are often asymptomatic with complaints that are caused by hormonal imbalance. Therefore, chromosome analysis needs t
Externí odkaz:
https://doaj.org/article/dbb6a3123169431ab278a91dbed6a6de
Autor:
Stefan Bagheri-Fam, Huijun Chen, Sean Wilson, Katie Ayers, James Hughes, Frederique Sloan-Bena, Pierre Calvel, Gorjana Robevska, Beatriz Puisac, Kamila Kusz-Zamelczyk, Stefania Gimelli, Anna Spik, Jadwiga Jaruzelska, Alina Warenik-Szymankiewicz, Sultana Faradz, Serge Nef, Juan Pié, Paul Thomas, Andrew Sinclair, Dagmar Wilhelm
Publikováno v:
PLoS ONE, Vol 15, Iss 1, p e0227411 (2020)
Disorders/differences of sex development (DSD) cause profound psychological and reproductive consequences for the affected individuals, however, most are still unexplained at the molecular level. Here, we present a novel gene, 3-hydroxy-3-methylgluta
Externí odkaz:
https://doaj.org/article/1d69a154859b4aa693da7b441971531f
Publikováno v:
Journal of Biomedicine and Translational Research. 8:149-154
Background: Couples unable to conceive and bear children could feel deep disappointment, often leading to depression. Infertility is one of the main reasons couples are not able to have children. Genetic counseling role in infertility ranges from exp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8ece7b426a68917c22e66816f5589cd7
https://doi.org/10.14710/jbtr.v8i3.16179
https://doi.org/10.14710/jbtr.v8i3.16179
Autor:
Iffa Mutmainah, Willy Nillesen, Farmaditya Mundhofir, Tri Winarni, Ineke van der Burgt, Helger Yntema, Sultana Faradz
Publikováno v:
Paediatrica Indonesiana, Vol 56, Iss 1, Pp 62-6 (2016)
Noonan syndrome (NS; OMIM#163950) is a relatively common autosomal dominant disorder with a worldwide prevalence of approximately 1:1,000 to 1:2,500. The syndrome is characterized by distinctive facial features, congenital heart defects (CHD), and sh
Externí odkaz:
https://doaj.org/article/c7bed8e85e94444dbb56a52b582962bd
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