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Author/Creator Haddadi, Mohammad

3. Biallelic missense variants in ZBTB11 can cause intellectual disability in humans. (8th June 2018)

Authors:
Fattahi, Zohreh; Sheikh, Taimoor I; Musante, Luciana; Rasheed, Memoona; Taskiran, Ibrahim Ihsan; Harripaul, Ricardo; Hu, Hao; Kazeminasab, Somayeh; Alam, Muhammad Rizwan; Hosseini, Masoumeh; Larti, Farzaneh; Ghaderi, Zhila; Celik, Arzu; Ayub, Muhammad; Ansar, Muhammad; Haddadi, Mohammad; Wienker,...
Journal:
Human molecular genetics
Issue:
Volume 27:Number 18(2018:Sep. 15)
Page Start:
3177
Record Type:
Journal Article
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4. CNKSR1 gene defect can cause syndromic autosomal recessive intellectual disability. Issue 8 (18th November 2018)

Authors:
Kazeminasab, Somayeh; Taskiran, Ibrahim Ihsan; Fattahi, Zohreh; Bazazzadegan, Niloofar; Hosseini, Masoumeh; Rahimi, Maryam; Oladnabi, Morteza; Haddadi, Mohammad; Celik, Arzu; Ropers, Hans‐Hilger; Najmabadi, Hossein; Kahrizi, Kimia
Journal:
American journal of medical genetics
Issue:
Volume 177:Issue 8(2018)
Page Start:
691
Record Type:
Journal Article
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7. Planktonic foraminiferal biostratigraphy of the upper Turonian-lower Santonian succession in the Lorestan Zone of the Zagros sedimentary Basin, SW Iran. (April 2023)

Authors:
Haddadi, Mohammad; Vahidinia, Mohammad; Gharaie, Mohamad Hosein Mahmudy; Ardestani, Meysam Shafiee; Bazeen, Youssef S.; Zaghbib-Turki, Dalila
Journal:
Journal of African earth sciences
Issue:
Volume 200(2023)
Page Start:
Record Type:
Journal Article
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