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Author/Creator Tavasoli, Behnaz

1. Molecular and clinical profile of congenital fibrinogen disorders in Iran, identification of two novel mutations. (8th July 2020)

Authors:
Tavasoli, Behnaz; Safa, Majid; Dorgalaleh, Akbar; Ghasemi, Jahan B.; Rezaei Makhouri, Farahnaz; Rezvani, Mohammad R.; Ahmadi, Abbas; Tabibian, Shadi; Jazebi, Mohammad; Baghaipour, Mohammad R.; Zaker, Farhad
Journal:
International journal of laboratory hematology
Issue:
Volume 42:Number 5(2020:Oct.)
Page Start:
619
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

2. Molecular basis of rare congenital bleeding disorders. (May 2023)

Authors:
Dorgalaleh, Akbar; Bahraini, Mehran; Shams, Mahmood; Parhizkari, Fereshteh; Dabbagh, Ali; Naderi, Tohid; Fallah, Aysan; Fazeli, Alieh; Ahmadi, Seyed Esmaeil; Samii, Amir; Daneshi, Maryam; Heydari, Farshad; Tabibian, Shadi; Tavasoli, Behnaz; Noroozi-Aghideh, Ali; Tabatabaei, Tahere; Gholami, Moham...
Journal:
Blood reviews
Issue:
Volume 59(2023)
Page Start:
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

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