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Author/Creator Fadaee, Mahsa

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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Available online (eLD content is only available in our Reading Rooms) ↗

2. Identification of disease‐causing variants in the EXOSC gene family underlying autosomal recessive intellectual disability in Iranian families. Issue 6 (14th May 2019)

Authors:
Beheshtian, Maryam; Fattahi, Zohreh; Fadaee, Mahsa; Vazehan, Raheleh; Jamali, Payman; Parsimehr, Elham; Kamgar, Mahboubeh; Zonooz, Mehrshid Faraji; Mahdavi, Shokouh Sadat; Kalhor, Zahra; Arzhangi, Sanaz; Abedini, Seyedeh Sedigheh; Kermani, Farahnaz Sabbagh; Mojahedi, Faezeh; Kalscheuer, Vera M.; ...
Journal:
Clinical genetics
Issue:
Volume 95:Issue 6(2019)
Page Start:
718
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

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