학술논문
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Börjeson–Forssman–Lehmann syndrome: delineating the clinical and allelic spectrum in 14 new families
Academic Journal
Jain, Vani; Foo, Seow Hoong; Chooi, Stephen; Moss, Celia; Goodwin, Richard; Berland, Siren; Clarke, Angus J.; Davies, Sally J.; Corrin, Sian; Murch, Oliver; Doyle, Samantha; Graham, Gail E.; Greenhalgh, Lynn; Holder, Susan E.; Johnson, Diana; Kumar, Ajith; Ladda, Roger L.; Sell, Susan; Begtrup, Amber; Lynch, Sally A.; McCann, Emma; Østern, Rune; Pottinger, Caroline; Splitt, Miranda; Fry, Andrew E.
European Journal of Human Genetics. 31(12):1421-1429
Academic Journal
Journal of Dental Education; Jul2021, Vol. 85 Issue 7, p1210-1216, 7p
Academic Journal
Faundes, Víctor; Jennings, Martin D.; Crilly, Siobhan; Legraie, Sarah; Withers, Sarah E.; Cuvertino, Sara; Davies, Sally J.; Douglas, Andrew G. L.; Fry, Andrew E.; Harrison, Victoria; Amiel, Jeanne; Lehalle, Daphné; Newman, William G.; Newkirk, Patricia; Ranells, Judith; Splitt, Miranda; Cross, Laura A.; Saunders, Carol J.; Sullivan, Bonnie R.; Granadillo, Jorge L.
Nature Communications; 2/5/2021, Vol. 12 Issue 1, p1-13, 13p
Academic Journal
Fry, Andrew E.; Marra, Christopher; Derrick, Anna V.; Pickrell, William O.; Higgins, Adam T.; te Water Naude, Johann; McClatchey, Martin A.; Davies, Sally J.; Metcalfe, Kay A.; Tan, Hui Jeen; Mohanraj, Rajiv; Avula, Shivaram; Williams, Denise; Brady, Lauren I.; Mesterman, Ronit; Tarnopolsky, Mark A.; Zhang, Yuehua; Yang, Ying; Wang, Xiaodong; Rees, Mark I.
Academic Journal
Faundes, Víctor; Newman, William G.; Bernardini, Laura; Canham, Natalie; Clayton-Smith, Jill; Dallapiccola, Bruno; Davies, Sally J.; Demos, Michelle K.; Goldman, Amy; Gill, Harinder; Horton, Rachel; Kerr, Bronwyn; Kumar, Dhavendra; Lehman, Anna; McKee, Shane; Morton, Jenny; Parker, Michael J.; Rankin, Julia; Robertson, Lisa; Temple, I. Karen
Academic Journal
BMC Medical Education; 2014 Suppl 1, Vol. 14, p1-6, 6p, 2 Charts
Academic Journal
Kielty, Cay M.; Davies, Sally J.; Phillips, Janet E.; Jones, Carolyn J. P.; Shuttleworth, C. Adrian; Charles, Stephen J.
Journal of Medical Genetics. Jan 01, 1995 32(1):1-6
Academic Journal
Isidor, Bertrand; Kuery, Sebastien; Rosenfeld, Jill A.; Besnard, Thomas; Schmitt, Sebastien; Joss, Shelagh; Davies, Sally J.; Lebel, Robert Roger; Henderson, Alex; Schaaf, Christian P.; Streff, Haley E.; Yang, Yaping; Jain, Vani; Chida, Nodoka; Latypova, Xenia; Le Caignec, Cedric; Cogne, Benjamin; Mercier, Sandra; Vincent, Marie; Colin, Estelle; Bonneau, Dominique; Denomme, Anne-Sophie; Parent, Philippe; Gilbert-Dussardier, Brigitte; Odent, Sylvie; Toutain, Annick; Piton, Amelie; Dina, Christian; Donnart, Audrey; Lindenbaum, Pierre; Charpentier, Eric; Redon, Richard; Iemura, Kenji; Ikeda, Masanori; Tanaka, Kozo; Bezieau, Stephane
Heimler Syndrome Is Caused by Hypomorphic Mutations in the Peroxisome-Biogenesis Genes PEX1 and PEX6
Academic Journal
Ratbi, Ilham; Falkenberg, Kim D.; Sommen, Manou; Al-Sheqaih, Nada; Guaoua, Soukaina; Vandeweyer, Geert; Urquhart, Jill E.; Chandler, Kate E.; Williams, Simon G.; Roberts, Neil A.; El Alloussi, Mustapha; Black, Graeme C.; Ferdinandusse, Sacha; Ramdi, Hind; Heimler, Audrey; Fryer, Alan; Lynch, Sally-Ann; Cooper, Nicola; Ong, Kai Ren; Smith, Claire E. L.; Inglehearn, Christopher F.; Mighell, Alan J.; Ecock, Claire; Poulter, James A.; Tischkowitz, Marc; Davies, Sally J.; Sefiani, Abdelaziz; Mironov, Aleksandr A.; Newman, William G.; Waterham, Hans R.; Van Camp, Guy
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[AR] Davies, Sally J.
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