المؤلفون: Van Allen, Margot I.

وصف الملف: text

الإتاحة: https://www.accessscience.com/content/article/a156500

المؤلفون: Jacquinet, Adeline, Brown, Lindsay, Sawkins, Jessica, Liu, Pengfei, Pugash, Denise, Van Allen, Margot I., Patel, Millan S.

المصدر: In European Journal of Medical Genetics May 2018 61(5):257-261

المؤلفون: Johnston, Jennifer J, Sapp, Julie C, Turner, Joyce T, Amor, David, Aftimos, Salim, Aleck, Kyrieckos A, Bocian, Maureen, Bodurtha, Joann N, Cox, Gerald F, Curry, Cynthia J, Day, Ruth, Donnai, Dian, Field, Michael, Fujiwara, Ikuma, Gabbett, Michael, Gal, Moran, Graham, John M, Hedera, Peter, Hennekam, Raoul CM, Hersh, Joseph H, Hopkin, Robert J, Kayserili, Hülya, Kidd, Alexa MJ, Kimonis, Virginia, Lin, Angela E, Lynch, Sally Ann, Maisenbacher, Melissa, Mansour, Sahar, McGaughran, Julie, Mehta, Lakshmi, Murphy, Helen, Raygada, Margarita, Robin, Nathaniel H, Rope, Alan F, Rosenbaum, Kenneth N, Schaefer, G Bradley, Shealy, Amy, Smith, Wendy, Soller, Maria, Sommer, Annmarie, Stalker, Heather J, Steiner, Bernhard, Stephan, Mark J, Tilstra, David, Tomkins, Susan, Trapane, Pamela, Tsai, Anne Chun‐Hui, Van Allen, Margot I, Vasudevan, Pradeep C, Zabel, Bernhard, Zunich, Janice, Black, Graeme CM, Biesecker, Leslie G

المصدر: Human Mutation. 31(10)

مصطلحات موضوعية: Genetics, Dental/Oral and Craniofacial Disease, Pediatric, Clinical Research, Rare Diseases, Congenital Structural Anomalies, Aetiology, 2.1 Biological and endogenous factors, Abnormalities, Multiple, Craniofacial Abnormalities, Genotype, Humans, Kruppel-Like Transcription Factors, Mouth Abnormalities, Mutation, Nerve Tissue Proteins, Pallister-Hall Syndrome, Phenotype, Polydactyly, Syndactyly, Zinc Finger Protein Gli3, GLI3, Greig syndrome, Pallister-Hall syndrome, oral-facial-digital syndrome, Clinical Sciences, Genetics & Heredity

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/6z17j09n

المؤلفون: Angius, Andrea, Uva, Paolo, Oppo, Manuela, Buers, Insa, Persico, Ivana, Onano, Stefano, Cuccuru, Gianmauro, Van Allen, Margot I., Hulait, Gurdip, Aubertin, Gudrun, Muntoni, Francesco, Fry, Andrew E., Annerén, Göran, 1945, Stattin, Evalena, Palomares-Bralo, Maria, Santos-Simarro, Fernando, Cucca, Francesco, Crisponi, Giangiorgio, Rutsch, Frank, Crisponi, Laura

المصدر: Clinical Genetics. 95(5):607-614

مصطلحات موضوعية: Crisponi, cold-induced sweating syndrome, CRLF1, MAGEL2, NALCN, SCN2A, whole exome sequencing

وصف الملف: print

URL الوصول: https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-382813

المؤلفون: Agochukwu, Nneamaka B., Solomon, Benjamin D., Zajaczkowska-Kielska, Anna, Lyons, Christopher J., Pollock, Travis, Singhal, Ash, Van Allen, Margot I., Muenke, Maximilian

المصدر: Child's Nervous System. December 2011 27(12):2183-2186

المؤلفون: Van Allen, Margot I., Boyle, Erin, Thiessen, Paul, McFadden, Deborah, Cochrane, Douglas, Chambers, G. Keith, Langlois, Sylvie, Stathers, Patricia, Irwin, Beverly, Cairns, Elizabeth, MacLeod, Patrick, Delisle, Marie -France, Uh, Soo -Hong

المصدر: Journal of Applied Genetics. June 2006 47(2):151-158

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المؤلفون: Bernard, Lynn E., McGillivray, Barbara, Van Allen, Margot I., Friedman, J. M., Langlois, Sylvie

المصدر: Journal of Genetic Counseling. February 1999 8(1):3-15

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