Substitutions in the Conserved C2C Domain of Otoferlin Cause DFNB9, a Form of Nonsyndromic Autosomal Recessive Deafness
Mirghomizadeh, F., Pfister, M., Apaydin, F., Petit, C., Kupka, S., Pusch, C.M., Zenner, H.P., Blin, N.
Published in Neurobiology of disease (01.07.2002)
Published in Neurobiology of disease (01.07.2002)
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Journal Article
Microsatellite and chromosome instability in squamous cell laryngeal carcinoma
Sasiadek, M, Stembalska-Kozlowska, A, Smigiel, R, Krecicki, T, Blin, N, Mirghomizadeh, F
Published in International journal of oncology (01.08.2001)
Published in International journal of oncology (01.08.2001)
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Journal Article
Klinische und molekulargenetische Analyse monozygoter Zwillinge mit Stapes-Gusher-Syndrom (DFN3)
OH, N, KUPKA, S, MIRGHOMIZADEH, F, AROLD, R, ZIMMERMANN, R, BLIN, N, ZENNER, H. P, PFISTER, M
Published in HNO (01.08.2003)
Published in HNO (01.08.2003)
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Journal Article
Correlation among loss of heterozygosity, promoter methylation and protein expression of MLH1 in larynx cancer
Smigiel, Robert, Stembalska-Kozlowska, Agnieszka, Mirghomizadeh, Farhad, Krecicki, Tomasz, Zatonski, Tomasz, Ramsey, David, Horobiowska, Monika, Jagielski, Jozef, Blin, Nikolaus, Sasiadek, Maria
Published in Oncology reports (01.03.2004)
Published in Oncology reports (01.03.2004)
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Journal Article
Second family with hearing impairment linked to 19q13 and refined DFNA4 localisation
Mirghomizadeh, Farhad, Bardtke, Bettina, Devoto, Marcella, Pfister, Markus, Oeken, Jens, König, Elke, Vitale, Emilia, Riccio, Antonio, De Rienzo, Assunta, Zenner, Hans Peter, Blin, Nikolaus
Published in European journal of human genetics : EJHG (01.02.2002)
Published in European journal of human genetics : EJHG (01.02.2002)
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Journal Article
Klinische und molekulargenetische Analyse monozygoter Zwillinge mit Stapes-Gusher-Syndrom (DFN3)
Oh, N., Kupka, S., Mirghomizadeh, F., Arold, R., Zimmermann, R., Blin, N., Zenner, H. P., Pfister, M.
Published in HNO (01.08.2003)
Published in HNO (01.08.2003)
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Journal Article
Clinical and molecular genetic analysis of monozygotic twins displaying stapes gusher syndrome (DFN3)
Oh, N, Kupka, S, Mirghomizadeh, F, Arold, R, Zimmermann, R, Blin, N, Zenner, H P, Pfister, M
Published in HNO (01.08.2003)
Published in HNO (01.08.2003)
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Journal Article
Mutationsanalyse des Connexin26-Gens bei sporadischen Fällen mittel- bis hochgradiger Schwerhörigkeit
Kupka, S., Mirghomizadeh, F., Haug, T., Braun, S., Leistenschneider, P., Schmitz-Salue, C., Arold, R., Blin, N., Zenner, H., Pfister, M.
Published in HNO (12.09.2000)
Published in HNO (12.09.2000)
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Journal Article
Mutational analysis of the connexin26 gene in sporadic cases of moderate to profound deafness
Kupka, S, Mirghomizadeh, F, Haug, T, Braun, S, Leistenschneider, P, Schmitz-Salue, C, Arold, R, Blin, N, Zenner, H P, Pfister, M
Published in HNO (01.09.2000)
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Published in HNO (01.09.2000)
Journal Article
Mutational analysis of the connexin26 gene in sporadic cases of moderate to profound deafness
Kupka, S, Mirghomizadeh, F, Haug, T, Braun, S, Leistenschneider, P, Schmitz-Salue, C, Arold, R, Blin, N, Zenner, H P, Pfister, M
Published in HNO (01.09.2000)
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Published in HNO (01.09.2000)
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