Genome-wide copy number variation analysis of a Branchio-oto-renal syndrome cohort identifies a recombination hotspot and implicates new candidate genes
Brophy, Patrick D., Alasti, Fatemeh, Darbro, Benjamin W., Clarke, Jason, Nishimura, Carla, Cobb, Bryan, Smith, Richard J., Manak, J. Robert
Published in Human genetics (01.12.2013)
Published in Human genetics (01.12.2013)
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A Mutation in HOXA2 Is Responsible for Autosomal-Recessive Microtia in an Iranian Family
Alasti, Fatemeh, Sadeghi, Abdorrahim, Sanati, Mohammad Hossein, Farhadi, Mohammad, Stollar, Elliot, Somers, Thomas, Van Camp, Guy
Published in American journal of human genetics (01.04.2008)
Published in American journal of human genetics (01.04.2008)
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Journal Article
A novel DFNA5 mutation does not cause hearing loss in an Iranian family
Van Laer, Lut, Meyer, Nicole C, Malekpour, Mahdi, Riazalhosseini, Yasser, Moghannibashi, Mahdi, Kahrizi, Kimia, Vandevelde, Ann, Alasti, Fatemeh, Najmabadi, Hossein, Van Camp, Guy, Smith, Richard J H
Published in Journal of human genetics (01.06.2007)
Published in Journal of human genetics (01.06.2007)
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Journal Article
A 1 bp deletion in the dual reading frame deafness gene LRTOMT causes a frameshift from the first into the second reading frame
Vanwesemael, Maarten, Schrauwen, Isabelle, Ceuppens, Ruben, Alasti, Fatemeh, Jorssen, Ellen, Farrokhi, Effat, Chaleshtori, Morteza Hashemzadeh, Van Camp, Guy
Published in American journal of medical genetics. Part A (01.08.2011)
Published in American journal of medical genetics. Part A (01.08.2011)
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Journal Article
A Mutation in HOXA2 Is Responsible for Autosomal-Recessive Microtia in an Iranian Family
Alasti, Fatemeh, Sadeghi, Abdorrahim, Sanati, Mohammad Hossein, Farhadi, Mohammad, Stollar, Elliot, Somers, Thomas, Van Camp, Guy
Published in American journal of human genetics (12.09.2008)
Published in American journal of human genetics (12.09.2008)
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Journal Article
A novel TECTA mutation confirms the recognizable phenotype among autosomal recessive hearing impairment families
Alasti, Fatemeh, Sanati, Mohammad Hossein, Behrouzifard, Amir Hossein, Sadeghi, Abdorrahim, de Brouwer, Arjan P.M, Kremer, Hannie, Smith, Richard J.H, Van Camp, Guy
Published in International journal of pediatric otorhinolaryngology (01.02.2008)
Published in International journal of pediatric otorhinolaryngology (01.02.2008)
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Journal Article
Identification of three novel TECTA mutations in Iranian families with autosomal recessive nonsyndromic hearing impairment at the DFNB21 locus
Meyer, Nicole C., Alasti, Fatemeh, Nishimura, Carla J., Imanirad, Parisa, Kahrizi, Kimia, Riazalhosseini, Yasser, Malekpour, Mahdi, Kochakian, Nafiseh, Jamali, Payman, Van Camp, Guy, Smith, Richard J.H., Najmabadi, Hossein
Published in American journal of medical genetics. Part A (15.07.2007)
Published in American journal of medical genetics. Part A (15.07.2007)
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Journal Article
Novel human pathological mutations. Gene symbol: SLC26A4. Disease: Pendred syndrome
Tabatabaiefar, Mohammad Amin, Alasti, Fatemeh, Peeters, Nils, Wuyts, Wim, Nooridaloii, Mohammad Reza, Chaleshtori, Morteza Hashemzadeh, Van Camp, Guy
Published in Human genetics (01.04.2010)
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Published in Human genetics (01.04.2010)
Journal Article
Mutation analysis of TMC1 identifies four new mutations and suggests an additional deafness gene at locus DFNA36-DFNB7/11: Four novel
Hilgert, Nele, Alasti, Fatemeh, Dieltjens, Nele, Pawlik, Barbara, Wollnik, Bernd, Uyguner, Oya, Delmaghani, Sedigheh, Weil, Dominique, Petit, Christine, Danis, Evi, Yang, Tao, Pandelia, Efthimia, Petersen, Michael B., Goossens, Dirk, Favero, Jurgen Del, Sanati, Mohammad Hossein, Smith, Richard JH, Van Camp, Guy
Published in Clinical genetics (09.07.2008)
Published in Clinical genetics (09.07.2008)
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Journal Article
Identification of three novel TECTA mutations in iranian families with autosomal recessive nonsyndromic hearing impairment at the DFNB21 locus: Special issue: The genetic basis of deafness
MEYER, Nicole C, ALASTI, Fatemeh, SMITH, Richard J. H, NAJMABADI, Hossein, NISHIMURA, Carla J, IMANIRAD, Parisa, KAHRIZI, Kimia, RIAZALHOSSEINI, Yasser, MALEKPOUR, Mahdi, KOCHAKIAN, Nafiseh, JAMALI, Payman, VAN CAMP, Guy
Published in American journal of medical genetics. Part A (2007)
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Published in American journal of medical genetics. Part A (2007)
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