Prelingual Deafness: High Prevalence of a 30delG Mutation in the Connexin 26 Gene
Denoyelle, Françoise, Weil, Dominique, Maw, Marion A., Wilcox, Stephen A., Lench, Nicholas J., Allen-Powell, Denise R., Osborn, Amelia H., Dahl, Hans-Henrik M., Middleton, Anna, Houseman, Mark J., Dodé, Catherine, Marlin, Sandrine, Boulila-ElGaïed, Amel, Grati, Mohammed, Ayadi, Hammadi, BenArab, Saïda, Bitoun, Pierre, Lina-Granade, Geneviève, Godet, Jacqueline, Mustapha, Mirna, Loiselet, Jacques, El-Zir, Élie, Aubois, Anne, Joannard, Alain, Levilliers, Jacqueline, Garabédian, Éréa-Noël, Mueller, Robert F., McKinlay Gardner, R. J., Petit, Christine
Published in Human molecular genetics (01.11.1997)
Published in Human molecular genetics (01.11.1997)
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A common founder for the 35delG GJB2 gene mutation in connexin 26 hearing impairment
VAN LAER, L, COUCKE, P, FRANSEN, E, ROWLAND, J, CUCCI, R. A, SMITH, R. J. H, VAN CAMP, G, MUELLER, R. F, CAETHOVEN, G, FLOTHMANN, K, PRASAD, S. D, CHAMBERLIN, G. P, HOUSEMAN, M, TAYLOR, G. R, VAN DE HEYNING, C. M
Published in Journal of medical genetics (01.08.2001)
Published in Journal of medical genetics (01.08.2001)
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Age as a Risk Factor for Complications Following Anterior Cervical Discectomy and Fusion: Analysis From the Michigan Spine Surgery Improvement Collaborative (MSSIC)
Lawless, Michael H, Tong, Doris, Claus, Chad F, Hanson, Connor, Li, Chenxi, Houseman, Clifford M, Bono, Peter, Richards, Boyd F, Kelkar, Prashant S, Abdulhak, Muwaffak M, Chang, Victor, Carr, Daniel A, Park, Paul, Soo, Teck M
Published in Spine (Philadelphia, Pa. 1976) (15.02.2022)
Published in Spine (Philadelphia, Pa. 1976) (15.02.2022)
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The Effect of Preoperative Symptom Duration on Patient-Reported Outcomes After Anterior Cervical Discectomy and Fusion in Nonmyelopathic Patients: Analyses From the Michigan Spine Surgery Improvement Collaborative (MSSIC)
Lawless, Michael H, Tong, Doris, Claus, Chad F, Hanson, Connor, Li, Chenxi, Park, Paul, Chang, Victor W, Abdulhak, Muwaffak M, Houseman, Clifford M, Bono, Peter L, Carr, Daniel A, Richards, Boyd F, Kelkar, Prashant S, Soo, Teck M
Published in Neurosurgery (01.05.2023)
Published in Neurosurgery (01.05.2023)
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Genetic analysis of the connexin-26 M34T variant: identification of genotype M34T/M34T segregating with mild-moderate non-syndromic sensorineural hearing loss
Houseman, Mark J, Ellis, Lucy A, Pagnamenta, Alistair, Di, Wei-Li, Rickard, Sarah, Osborn, Amelia H, Dahl, Hans-Henrik M, Taylor, Graham R, Bitner-Glindzicz, Maria, Reardon, William, Mueller, Robert F, Kelsell, David P
Published in Journal of medical genetics (01.01.2001)
Published in Journal of medical genetics (01.01.2001)
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Connexin Mutations in Skin Disease and Hearing Loss
Kelsell, David P., Di, Wei-Li, Houseman, Mark J.
Published in American journal of human genetics (01.03.2001)
Published in American journal of human genetics (01.03.2001)
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A case of erythrokeratoderma variabilis without mutations in connexin 31
Ishida‐Yamamoto, A., Kelsell, D., Common, J., Houseman, M.J., Hashimoto, M., Shibaki, H., Asano, K., Takahashi, H., Hashimoto, Y., Senshu, T., Leigh, I.M., Iizuka, H.
Published in British journal of dermatology (1951) (01.12.2000)
Published in British journal of dermatology (1951) (01.12.2000)
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Radiographic and Patient-Reported Outcomes of Lordotic Versus Non-lordotic Static Interbody Devices in Minimally Invasive Transforaminal Lumbar Interbody Fusion: A Longitudinal Comparative Cohort Study
Lawless, Michael H, Claus, Chad F, Tong, Doris, Jordan, Noah, Dosanjh, Amarpal, Hanson, Connor T, Carr, Daniel A, Houseman, Clifford M
Published in Curēus (Palo Alto, CA) (15.01.2022)
Published in Curēus (Palo Alto, CA) (15.01.2022)
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Bone morphogenetic protein in the repair of cerebrospinal fluid leak after transsphenoidal surgery
Slavnic, Dejan, Cook, Richard, Bahoura, Matthew, Paik, Gijong, Tong, Doris, Houseman, Clifford, Barrett, Ryan, Soo, Teck-Mun
Published in Asian journal of neurosurgery (01.04.2019)
Published in Asian journal of neurosurgery (01.04.2019)
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Congenital non-syndromal sensorineural hearing impairment due to connexin 26 gene mutations — molecular and audiological findings
Mueller, R.F, Nehammer, A, Middleton, A, Houseman, M, Taylor, G.R, Bitner-Glindzciz, M, Van Camp, G, Parker, M, Young, I.D, Davis, A, Newton, V.E, Lench, N.J
Published in International journal of pediatric otorhinolaryngology (15.10.1999)
Published in International journal of pediatric otorhinolaryngology (15.10.1999)
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A new locus for autosomal recessive non-syndromal sensorineural hearing impairment (DFNB27) on chromosome 2q23-q31
Pulleyn, L J, Jackson, A P, Roberts, E, Carridice, A, Muxworthy, C, Houseman, M, Al-Gazali, L I, Lench, N J, Markham, A F, Mueller, R F
Published in European journal of human genetics : EJHG (01.12.2000)
Published in European journal of human genetics : EJHG (01.12.2000)
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Species Diversity and Intraspecific Genetic Variation of Reticulitermes (Isoptera: Rhinotermitidae) Subterranean Termites in Woodland and Urban Environments of Missouri
Pinzon, Olga P., Houseman, Richard M.
Published in Annals of the Entomological Society of America (01.09.2009)
Published in Annals of the Entomological Society of America (01.09.2009)
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A new locus for non-syndromal, autosomal recessive, sensorineural hearing loss (DFNB16) maps to human chromosome 15q21-q22
Campbell, D A, McHale, D P, Brown, K A, Moynihan, L M, Houseman, M, Karbani, G, Parry, G, Janjua, A H, Newton, V, al-Gazali, L, Markham, A F, Lench, N J, Mueller, R F
Published in Journal of medical genetics (01.12.1997)
Published in Journal of medical genetics (01.12.1997)
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Preoperative Symptom Duration as a Predictor for Patient-Reported-Outcomes in Anterior Cervical Discectomy and Fusion in Non-Myelopathic Patients: Analysis from the Michigan Spine Surgery Improvement Collaborative (MSSIC)
Lawless, Michael H, Claus, Chad F, Tong, Doris, Bahoura, Matthew, Garmo, Lucas, Li, Chenxi, Houseman, Clifford M, Bono, Peter L, Richards, Boyd F, Kelkar, Prashant S, Park, Paul, Abdulhak, Muwaffak, Chang, Victor W, Soo, Teck M
Published in Neurosurgery (01.12.2020)
Published in Neurosurgery (01.12.2020)
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