Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Denise R. Allen"'
Autor:
David C. Shih, Rachel Silver, Olga L. Henao, Aynalem Alemu, Allan Audi, Godfrey Bigogo, Josh M. Colston, Elijah P. Edu-Quansah, Timothy A. Erickson, Andargachew Gashu, G. Burgess Gbelee, Sarah M. Gunter, Margaret N. Kosek, Gorbee G. Logan, Joy M. Mackey, Adrianna Maliga, Russell Manzanero, Gerhaldine Morazan, Francis Morey, Flor M. Munoz, Kristy O. Murray, Thelma V. Nelson, Maribel Paredes Olortegui, Pablo Penataro Yori, Shannon E. Ronca, Francesca Schiaffino, Adamu Tayachew, Musse Tedasse, Mesfin Wossen, Denise R. Allen, Pawan Angra, Amanda Balish, Madeline Farron, Marta Guerra, Amy Herman-Roloff, Victoria J. Hicks, Elizabeth Hunsperger, Lilit Kazazian, Matt Mikoleit, Peninah Munyua, Patrick K. Munywoki, Angella Sandra Namwase, Clayton O. Onyango, Michael Park, Leonard F. Peruski, David E. Sugerman, Emily Zielinski Gutierrez, Adam L. Cohen
Publikováno v:
Emerging Infectious Diseases, Vol 28, Iss 13, Pp 34-41 (2022)
Existing acute febrile illness (AFI) surveillance systems can be leveraged to identify and characterize emerging pathogens, such as SARS-CoV-2, which causes COVID-19. The US Centers for Disease Control and Prevention collaborated with ministries of h
Externí odkaz:
https://doaj.org/article/d275936d90f44eca86a8c78f007680c6
Autor:
Denise R. Allen-Powell, Kevin B. Sevior, Yelena Bykhovskaya, Atsushi Hatamochi, Ian Stewart, Nathan Fischel-Ghodsian, Marion A. Maw
Publikováno v:
American Journal of Medical Genetics. 75:179-185
A New Zealand and a Scottish pedigree with maternally inherited sensorineural deafness were both previously shown to carry a heteroplasmic A7445G mutation in the mitochondrial genome. More detailed clinical examination of the New Zealand family showe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e604022ae4e977230c31f7e238d2c251
https://doi.org/10.1002/(sici)1096-8628(19980113)75:2<179::aid-ajmg11>3.0.co
https://doi.org/10.1002/(sici)1096-8628(19980113)75:2<179::aid-ajmg11>3.0.co
Autor:
Mohammed Grati, Pierre Bitoun, Saida Benarab, Stephen A. Wilcox, Christine Petit, Alain Joannard, Amel Boulila-Elgaied, Elie El-Zir, J Godet, Mirna Mustapha, Hans Henrik M. Dahl, Jacqueline Levilliers, Denise R. Allen-Powell, Nicholas Lench, Jacques Loiselet, Anna Middleton, Mark J. Houseman, Hammadi Ayadi, Marion A. Maw, Robert F. Mueller, Catherine Dodé, Amelia H. Osborn, Françoise Denoyelle, Dominique Weil, R. J McKinlay Gardner, Anne Aubois, Geneviève Lina-Granade, Erea Noel Garabedian, Sandrine Marlin
Publikováno v:
Human Molecular Genetics. 6:2173-2177
Prelingual non-syndromic (isolated) deafness is the most frequent hereditary sensory defect. In >80% of the cases, the mode of transmission is autosomal recessive. To date, 14 loci have been identified for the recessive forms (DFNB loci). For two of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8b520ebc61e08e77e5a44e9222355385
https://doi.org/10.1093/hmg/6.12.2173
https://doi.org/10.1093/hmg/6.12.2173