Results 1 -
9
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9
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Kahrizi syndrome
- ... Central Zhang Y, Malekpour M, Al-Madani N, Kahrizi K, Zanganeh M, Lohr NJ, Mohseni M, Mojahedi F, Daneshi A, Najmabadi H, Smith RJ. Sensorineural deafness and male infertility: a contiguous gene deletion syndrome. J Med Genet. 2007 Apr;44(4):233- ...
- ... Central Zhang Y, Malekpour M, Al-Madani N, Kahrizi K, Zanganeh M, Lohr NJ, Mohseni M, Mojahedi F, Daneshi A, Najmabadi H, Smith RJ. Sensorineural deafness and male infertility: a contiguous gene deletion syndrome. J Med Genet. 2007 Apr;44(4):233- ...
- ... Central Zhang Y, Malekpour M, Al-Madani N, Kahrizi K, Zanganeh M, Lohr NJ, Mohseni M, Mojahedi F, Daneshi A, Najmabadi H, Smith RJ. Sensorineural deafness and male infertility: a contiguous gene deletion syndrome. J Med Genet. 2007 Apr;44(4):233- ...
- ... Central Zhang Y, Malekpour M, Al-Madani N, Kahrizi K, Zanganeh M, Lohr NJ, Mohseni M, Mojahedi F, Daneshi A, Najmabadi H, Smith RJ. Sensorineural deafness and male infertility: a contiguous gene deletion syndrome. J Med Genet. 2007 Apr;44(4):233- ...
- ... on PubMed Moheb LA, Tzschach A, Garshasbi M, Kahrizi K, Darvish H, Heshmati Y, Kordi A, Najmabadi H, Ropers HH, Kuss AW. Identification of a nonsense mutation in the very low-density lipoprotein receptor gene (VLDLR) in an Iranian family with dysequilibrium syndrome. Eur J Hum Genet. 2008 Feb;16(2): ...
- ... PubMed Central Moheb LA, Tzschach A, Garshasbi M, Kahrizi K, ... Iranian family with dysequilibrium syndrome. Eur J Hum Genet. 2008 Feb;16(2): ...
- ... Condition DFNA11 DFNB2 MYO7A_HUMAN myosin VIIA (Usher syndrome 1B (autosomal recessive, severe)) NSRD2 USH1B Tests of MYO7A PubMed MYOSIN VIIA; MYO7A NCBI Gene ClinVar Hildebrand MS, Thorne NP, Bromhead CJ, Kahrizi K, Webster JA, Fattahi Z, Bataejad M, Kimberling ...
- ... X-LINKED; ARX NCBI Gene ClinVar Abedini SS, Kahrizi K, Behjati F, Banihashemi S, Ghasemi Firoozabadi S, ...
- ... or Free article on PubMed Central Chen W, Kahrizi K, Meyer NC, Riazalhosseini Y, Van Camp G, ... COL11A2 mutation associated with autosomal recessive Weissenbacher-Zweymuller syndrome: molecular and clinical overlap with otospondylomegaepiphyseal dysplasia (OSMED). ...
