Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Oumarou Diallo"'
Publikováno v:
Canadian Journal of Animal Science. 100:739-744
Cette étude vise à estimer le poids du fœtus zébu peulh à partir des mesures échographiques des diamètres de l’abdomen (DA), du bipariétal (DBP), du cordon ombilical (DCO), de la corne utérine (DCU) et des longueurs du fémur (LF), du tibi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a715186aa44df17d23cce392a964a10c
https://doi.org/10.1139/cjas-2020-0004
https://doi.org/10.1139/cjas-2020-0004
Autor:
Jeremy M. Sullivan, J. Raphael Gibbs, Christy L. Ludlow, Barrington G. Burnett, Charlotte J. Sumner, Yijun Shi, Janel O. Johnson, Guida Landouré, Oumarou Diallo, Bryan J. Traynor, Kenneth H. Fischbeck, Rachelle Gaudet, Clare H. Munns
Publikováno v:
Neurology. 79:192-194
Mutations in over 50 genes have been associated with Charcot-Marie-Tooth (CMT) disease. As new genes continue to be discovered, the task of sequencing each of them individually with traditional techniques becomes increasingly burdensome. In addition,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::422c0c3fd369cf0f54ce0230374dbab6
https://doi.org/10.1212/wnl.0b013e31825f04b2
https://doi.org/10.1212/wnl.0b013e31825f04b2
Autor:
Tyler Mark Pierson, Stephan Züchner, Oumarou Diallo, Katherine V. Bricceno, Nichole D. Hein, Camilo Toro, Craig Blackstone, Bryan J. Traynor, Kenneth H. Fischbeck, Katherine G. Meilleur, Shoji Tsuji, Dennis M.D. Landis, William A. Gahl, Hiroyuki Ishiura, Charles Marques Lourenço, Janel O. Johnson, Guida Landouré, Giovanni Stevanin, Peng Peng Zhu, Garth A. Nicholson, Carlo Rinaldi, Wilson Marques, Modibo Sangare, Fiorella Speziani, Leslie G. Biesecker, Barrington G. Burnett, John K. Fink, John Accardi, Michael A. Gonzalez, Alexandra Durr, Marion Stoll
Publikováno v:
Human mutation, vol 34, iss 10
We report here the genetic basis for a form of progressive hereditary spastic paraplegia (SPG43) previously described in two Malian sisters. Exome sequencing revealed a homozygous missense variant (c.187G>C; p.Ala63Pro) in C19orf12, a gene recently i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f85389feab47227efe45546b8cd1b162
https://europepmc.org/articles/PMC3819934/
https://europepmc.org/articles/PMC3819934/
