Items where Author is "Ahangari, N."

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Number of items: 4.

Article

Hedberg-Oldfors, C. and Abramsson, A. and Osborn, D. P. S. and Danielsson, O. and Fazlinezhad, A. and Nilipour, Y. and Hübbert, L. and Nennesmo, I. and Visuttijai, K. and Bharj, J. and Petropoulou, E. and Shoreim, A. and Vona, B. and Ahangari, N. and López, M. D. and Doosti, M. and Banote, R. K. and Maroofian, R. and Edling, M. and Taherpour, M. and Zetterberg, H. and Karimiani, E. G. and Oldfors, A. and Jamshidi, Y. (2019) Cardiomyopathy with lethal arrhythmias associated with inactivation of KLHL24. Human Molecular Genetics, 28 (11). pp. 1919-1929.

Lekszas, C. and Nanda, I. and Vona, B. and Böck, J. and Ashrafzadeh, F. and Donyadideh, N. and Ebrahimzadeh, F. and Ahangari, N. and Maroofian, R. and Karimiani, E. G. and Haaf, T. (2019) Unbalanced segregation of a paternal t(9;11)(p24.3;p15.4) translocation causing familial Beckwith-Wiedemann syndrome: A case report. BMC Medical Genomics, 12 (1).

Makrythanasis, P. and Maroofian, R. and Stray-Pedersen, A. and Musaev, D. and Zaki, M. S. and Mahmoud, I. G. and Selim, L. and Elbadawy, A. and Jhangiani, S. N. and Coban Akdemir, Z. H. and Gambin, T. and Sorte, H. S. and Heiberg, A. and McEvoy-Venneri, J. and James, K. N. and Stanley, V. and Belandres, D. and Guipponi, M. and Santoni, F. A. and Ahangari, N. and Tara, F. and Doosti, M. and Iwaszkiewicz, J. and Zoete, V. and Backe, P. H. and Hamamy, H. and Gleeson, J. G. and Lupski, J. R. and Karimiani, E. G. and Antonarakis, S. E. (2018) Biallelic variants in KIF14 cause intellectual disability with microcephaly. European Journal of Human Genetics, 26 (3). pp. 330-339.

Vona, B. and Maroofian, R. and Bellacchio, E. and Najafi, M. and Thompson, K. and Alahmad, A. and He, L. and Ahangari, N. and Rad, A. and Shahrokhzadeh, S. and Bahena, P. and Mittag, F. and Traub, F. and Movaffagh, J. and Amiri, N. and Doosti, M. and Boostani, R. and Shirzadeh, E. and Haaf, T. and Diodato, D. and Schmidts, M. and Taylor, R. W. and Karimiani, E. G. (2018) Expanding the clinical phenotype of IARS2-related mitochondrial disease. BMC medical genetics, 19 (1). p. 196.

This list was generated on Fri Jul 3 13:13:20 2020 EDT.