Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Niaz Ahankoob"'
Autor:
Niaz Ahankoob, Vincent P. Stahel
Publikováno v:
Patient Safety in Surgery, Vol 16, Iss 1, Pp 1-6 (2022)
Abstract Background Bone adhesives have been on the forefront of orthopedic surgery research for decades due to the potential benefit they may have in fracture management. Current publications and research being conducted on bone adhesive could be ap
Externí odkaz:
https://doaj.org/article/4ed293404f15471c9804cee0e535d0a6
Publikováno v:
Patient Safety in Surgery, Vol 16, Iss 1, Pp 1-4 (2022)
Externí odkaz:
https://doaj.org/article/f5dd81a0fe154fecbdd2de52fa9f3d55
Autor:
Charles E. Robertson, Alessandra Nadine E. Chiong, Michèle M. Sale, Nanette R. Lee, Kimberly Mae C. Ong, Sairah Yousaf, Jose Pedrito M. Magno, Diana Ir, Patrick John Labra, Petri S. Mattila, Maria Luz San Agustin, Generoso T. Abes, Erasmo Gonzalo D V Llanes, Ma. Carmina Espiritu-Chiong, Maria Rina T. Reyes-Quintos, Tori C. Bootpetch, Wasyl Szeremeta, Allen F. Ryan, Teresa Luisa G. Cruz, Arnaud P. J. Giese, Suzanne M. Leal, Rachelle Marie A. Nonato, Zubair M. Ahmed, Abner L. Chan, Karen L. Mohlke, Rhodieleen Anne R. de la Cruz, Regie Lyn P. Santos-Cortez, Matthew J. Steritz, Tasnee Chonmaitree, Daniel N. Frank, Eva Maria Cutiongco-de la Paz, Melquiadesa Pedro, Elisabet Einarsdottir, Talitha Karisse L. Yarza, Juha Kere, Deborah A. Nickerson, Lena Hafrén, Niaz Ahankoob, Michael J. Bamshad, Kathleen Daly, Ma. Leah C. Tantoco, Charlotte M. Chiong, Harold S. Pine, Saima Riazuddin
Publikováno v:
Journal of Medical Genetics. 58:442-452
BackgroundOtitis media (OM) susceptibility has significant heritability; however, the role of rare variants in OM is mostly unknown. Our goal is to identify novel rare variants that confer OM susceptibility.MethodsWe performed exome and Sanger sequen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4c1f3273286a54b911b866b3c1c6e874
https://doi.org/10.1136/jmedgenet-2020-106844
https://doi.org/10.1136/jmedgenet-2020-106844
Autor:
Daniel N, Frank, Arnaud P J, Giese, Lena, Hafren, Tori C, Bootpetch, Talitha Karisse L, Yarza, Matthew J, Steritz, Melquiadesa, Pedro, Patrick John, Labra, Kathleen A, Daly, Ma Leah C, Tantoco, Wasyl, Szeremeta, Maria Rina T, Reyes-Quintos, Niaz, Ahankoob, Erasmo Gonzalo D V, Llanes, Harold S, Pine, Sairah, Yousaf, Diana, Ir, Elisabet, Einarsdottir, Rhodieleen Anne R, de la Cruz, Nanette R, Lee, Rachelle Marie A, Nonato, Charles E, Robertson, Kimberly Mae C, Ong, Jose Pedrito M, Magno, Alessandra Nadine E, Chiong, Ma Carmina, Espiritu-Chiong, Maria Luz, San Agustin, Teresa Luisa G, Cruz, Generoso T, Abes, Michael J, Bamshad, Eva Maria, Cutiongco-de la Paz, Juha, Kere, Deborah A, Nickerson, Karen L, Mohlke, Saima, Riazuddin, Abner, Chan, Petri S, Mattila, Suzanne M, Leal, Allen F, Ryan, Zubair M, Ahmed, Tasnee, Chonmaitree, Michele M, Sale, Charlotte M, Chiong, Regie Lyn P, Santos-Cortez
Publikováno v:
J Med Genet
BACKGROUND: Otitis media (OM) susceptibility has significant heritability, however the role of rare variants in OM is mostly unknown. Our goal is to identify novel rare variants that confer OM susceptibility. METHODS: We performed exome and Sanger se
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b44b2d0faca9516c60eb8a0c6d7e44ef
https://pubmed.ncbi.nlm.nih.gov/32709676
https://pubmed.ncbi.nlm.nih.gov/32709676