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Exome sequencing utility in defining the genetic landscape of hearing loss and novel‐gene discovery in Iran von Mohseni, Marzieh, Babanejad, Mojgan, Booth, Kevin T., Jamali, Payman, Jalalvand, Khadijeh, Davarnia, Behzad, Ardalani, Fariba, Khoshaeen, Atefeh, Arzhangi, Sanaz, Ghodratpour, Fatemeh, Beheshtian, Maryam, Jahanshad, Faezeh, Otukesh, Hasan, Bahrami, Fatemeh, Seifati, Seyed Morteza, Bazazzadegan, Niloofar, Habibi, Farkhonde, Behravan, Hanieh, Mirzaei, Sepide, Keshavarzi, Fatemeh, Nikzat, Nooshin, Mehrjoo, Zohreh, Thiele, Holger, Nothnagel, Michael, Azaiez, Hela, Smith, Richard J., Kahrizi, Kimia, Najmabadi, Hossein
Veröffentlicht in Clinical genetics
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Seite wird neu geladen, wenn Filter aktiviert oder ausgeschlossen wird.- Adolescent 1 Treffer 1
- Adult 1 Treffer 1
- Child 1 Treffer 1
- Child, Preschool 1 Treffer 1
- Cohort Studies 1 Treffer 1
- Consanguinity 1 Treffer 1
- Deafness 1 Treffer 1
- Dna Sequencing 1 Treffer 1
- Etiology 1 Treffer 1
- Exome - Genetics 1 Treffer 1
- Exome Sequencing 1 Treffer 1
- Exome Sequencing - Methods 1 Treffer 1
- Female 1 Treffer 1
- Gene Discovery 1 Treffer 1
- Genes 1 Treffer 1
- Genetic Predisposition To Disease - Genetics 1 Treffer 1
- Genetics & Heredity 1 Treffer 1
- Hearing Loss 1 Treffer 1
- Hearing Loss - Genetics 1 Treffer 1
- High-Throughput Nucleotide Sequencing - Methods 1 Treffer 1