The Meckel-Gruber Syndrome proteins MKS1 and meckelin interact and are required for primary cilium formation
Dawe, Helen R., Smith, Ursula M., Cullinane, Andrew R., Gerrelli, Dianne, Cox, Phillip, Badano, Jose L., Blair-Reid, Sarah, Sriram, Nisha, Katsanis, Nicholas, Attie-Bitach, Tania, Afford, Simon C., Copp, Andrew J., Kelly, Deirdre A., Gull, Keith, Johnson, Colin A.
Published in Human molecular genetics (15.01.2007)
Published in Human molecular genetics (15.01.2007)
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The Meckel-Gruber Syndrome Gene, MKS3, Is Mutated in Joubert Syndrome
Baala, Lekbir, Romano, Stéphane, Khaddour, Rana, Saunier, Sophie, Smith, Ursula M., Audollent, Sophie, Ozilou, Catherine, Faivre, Laurence, Laurent, Nicole, Foliguet, Bernard, Munnich, Arnold, Lyonnet, Stanislas, Salomon, Rémi, Encha-Razavi, Férechté, Gubler, Marie-Claire, Boddaert, Nathalie, de Lonlay, Pascale, Johnson, Colin A., Vekemans, Michel, Antignac, Corinne, Attié-Bitach, Tania
Published in American journal of human genetics (01.01.2007)
Published in American journal of human genetics (01.01.2007)
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The transmembrane protein meckelin ( MKS3 ) is mutated in Meckel-Gruber syndrome and the wpk rat
Bennett, Christopher P, Attie-Bitach, Tania, Lilliquist, Stacie, Pasha, Shanaz, Harris, Peter C, Morgan, Neil V, Malik Sharif, Saghira, Maher, Eamonn R, Johnson, Colin A, Tee, Louise J, Maina, Esther N, Bucourt, Martine, Miller, Caroline A, Ward, Christopher J, Goranson, Erin, Trembath, Richard C, McKee, Brandy M, McKeown, Carole, Consugar, Mark, Torres, Vicente E, Cox, Phillip, Smith, Ursula M, Gattone, Vincent H, Whelan, Shelly, Aligianis, Irene A, Batman, Philip A, Woods, C Geoffrey, AlGazali, Lihadh, Punyashthiti, Rachaneekorn, Gissen, Paul, Kelly, Deirdre A
Published in Nature genetics (01.02.2006)
Published in Nature genetics (01.02.2006)
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Autozygosity mapping of Bardet-Biedl syndrome to 12q21.2 and confirmation of FLJ23560 as BBS10
White, Dominic R A, Ganesh, Anuradha, Nishimura, Darryl, Rattenberry, Eleanor, Ahmed, Shakeel, Smith, Ursula M, Pasha, Shanaz, Raeburn, Sandy, Trembath, Richard C, Rajab, Anna, Macdonald, Fiona, Banin, Eyal, Stone, Edwin M, Johnson, Colin A, Sheffield, Val C, Maher, Eamonn R
Published in European journal of human genetics : EJHG (01.02.2007)
Published in European journal of human genetics : EJHG (01.02.2007)
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Peak Serum Estradiol Level During Controlled Ovarian Stimulation Is not Associated with Lower Levels of Pregnancy-Associated Plasma Protein-A or Small for Gestational Age Infants: A Cohort Study
Dunne, Caitlin, MD, Cho, Kristy, MD, Shan, Angel, MD, Hutcheon, Jennifer, PhD, Durland, Ursula Smith, MS, Seethram, Ken, MD, Havelock, Jon C., MD
Published in Journal of obstetrics and gynaecology Canada (01.10.2017)
Published in Journal of obstetrics and gynaecology Canada (01.10.2017)
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Journal Article
Autozygosity mapping of Bardet-Biedl syndrome to 12q21.2 and confirmation of FLJ23560 as BBS10
White, Dominic R A, Ganesh, Anuradha, Nishimura, Darryl, Rattenberry, Eleanor, Ahmed, Shakeel, Smith, Ursula M, Pasha, Shanaz, Raeburn, Sandy, Trembath, Richard C, Rajab, Anna, Macdonald, Fiona, Banin, Eyal, Stone, Edwin M, Johnson, Colin A, Sheffield, Val C, Maher, Eamonn R
Published in European journal of human genetics : EJHG (01.02.2007)
Published in European journal of human genetics : EJHG (01.02.2007)
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