Author/Creator: Saat, Hanife - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Author/Creator Saat, Hanife

1. Confirmation of the prenatal mosaic trisomy 2 via fetal USG and cytogenetic analyses. (3rd July 2017)

Authors:: Tuğ, Esra; Karcaaltincaba, Deniz; Yirmibeş Karaoğuz, Meral; Saat, Hanife; Özek, Aykut
Journal:: Journal of maternal-fetal & neonatal medicine
Issue:: Volume 30:Number 13(2017)
Page Start:: 1579
Record Type:: Journal Article
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2. Melanocortin 3 receptor gene polymorphism is associated with polycystic ovary syndrome in Turkish population. (3rd August 2019)

Authors:: Hepsen, Sema; Cakal, Erman; Karakose, Melia; Eyerci, Nilnur; Saat, Hanife; Beysel, Selvihan; Oztekin, Sanem; Pinarli, Ferda; Parlak, Mesut
Journal:: Gynecological endocrinology
Issue:: Volume 35:Number 8(2019)
Page Start:: 685
Record Type:: Journal Article
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3. Mutation spectrum of hereditary myopathies in Turkish patients and novel variants. (8th May 2021)

Authors:: Saat, Hanife; Sahin, Ibrahim
Journal:: Annals of human genetics
Issue:: Volume 85:Number 5(2021)
Page Start:: 178
Record Type:: Journal Article
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