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Author/Creator Mehvari, Sepideh

1. Comprehensive genotype‐phenotype correlation in AP‐4 deficiency syndrome; Adding data from a large cohort of Iranian patients. Issue 1 (14th September 2020)

Authors:
Beheshtian, Maryam; Akhtarkhavari, Tara; Mehvari, Sepideh; Mohseni, Marzieh; Fattahi, Zohreh; Abedini, Seyedeh Sedigheh; Arzhangi, Sanaz; Fadaee, Mahsa; Jamali, Payman; Najafipour, Reza; Kalscheuer, Vera M.; Hu, Hao; Ropers, Hans‐Hilger; Najmabadi, Hossein; Kahrizi, Kimia
Journal:
Clinical genetics
Issue:
Volume 99:Issue 1(2021)
Page Start:
187
Record Type:
Journal Article
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2. Effect of inbreeding on intellectual disability revisited by trio sequencing. Issue 1 (19th November 2018)

Authors:
Kahrizi, Kimia; Hu, Hao; Hosseini, Masoumeh; Kalscheuer, Vera M.; Fattahi, Zohreh; Beheshtian, Maryam; Suckow, Vanessa; Mohseni, Marzieh; Lipkowitz, Bettina; Mehvari, Sepideh; Mehrjoo, Zohreh; Akhtarkhavari, Tara; Ghaderi, Zhila; Rahimi, Maryam; Arzhangi, Sanaz; Jamali, Payman; Falahat Chian, Mil...
Journal:
Clinical genetics
Issue:
Volume 95:Issue 1(2019)
Page Start:
151
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

3. Whole genome sequencing identifies a duplicated region encompassing Xq13.2q13.3 in a large Iranian family with intellectual disability. Issue 10 (26th July 2020)

Authors:
Mehvari, Sepideh; Larti, Farzaneh; Hu, Hao; Fattahi, Zohreh; Beheshtian, Maryam; Abedini, Seyedeh Sedigheh; Arzhangi, Sanaz; Ropers, Hans‐Hilger; Kalscheuer, Vera M.; Auld, Daniel; Kahrizi, Kimia; Riazalhosseini, Yasser; Najmabadi, Hossein
Journal:
Molecular genetics & genomic medicine
Issue:
Volume 8:Issue 10(2020)
Page Start:
n/a
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗