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Author/Creator Fattahi, Z.

1. Autosomal recessive mutations in THOC6 cause intellectual disability: syndrome delineation requiring forward and reverse phenotyping. Issue 1 (24th May 2016)

Authors:
Amos, J.S.; Huang, L.; Thevenon, J.; Kariminedjad, A.; Beaulieu, C.L.; Masurel‐Paulet, A.; Najmabadi, H.; Fattahi, Z.; Beheshtian, M.; Tonekaboni, S.H.; Tang, S.; Helbig, K.L.; Alcaraz, W.; Rivière, J.‐B.; Faivre, L.; Innes, A.M.; Lebel, R.R.; Boycott, K.M.
Journal:
Clinical genetics
Issue:
Volume 91:Issue 1(2017)
Page Start:
92
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

2. Improved diagnostic yield of neuromuscular disorders applying clinical exome sequencing in patients arising from a consanguineous population. Issue 3 (21st July 2016)

Authors:
Fattahi, Z.; Kalhor, Z.; Fadaee, M.; Vazehan, R.; Parsimehr, E.; Abolhassani, A.; Beheshtian, M.; Zamani, G.; Nafissi, S.; Nilipour, Y.; Akbari, M.R.; Kahrizi, K.; Kariminejad, A.; Najmabadi, H.
Journal:
Clinical genetics
Issue:
Volume 91:Issue 3(2017)
Page Start:
386
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

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