المؤلفون: Jie Xu, Catherine Brownstein, Sarah Ossler, Catherine Melver

المصدر: Genetics in Medicine Open, Vol 1, Iss 1, Pp 100390- (2023)

مصطلحات موضوعية: Genetics, QH426-470, Medicine

وصف الملف: electronic resource

Relation: http://www.sciencedirect.com/science/article/pii/S2949774423003904; https://doaj.org/toc/2949-7744

URL الوصول: https://doaj.org/article/b034fdfa73904146872c88d19178d021

المؤلفون: Angela Peron, Felice D'Arco, Kimberly A. Aldinger, Constance Smith-Hicks, Christiane Zweier, Gyri A. Gradek, Kimberley Bradbury, Andrea Accogli, Erica F. Andersen, Ping Yee Billie Au, Roberta Battini, Daniah Beleford, Lynne M. Bird, Arjan Bouman, Ange-Line Bruel (O)yvind L(o)vold Busk, Philippe M. Campeau, Valeria Capra, Colleen Carlston, Jenny Carmichael, Anna Chassevent, Jill Clayton-Smith, Michael J Bamshad, Dawn L. Earl, Laurence Faivre, Christophe Philippe, Patrick Ferrerira, Luitgard Graul-Neumann, Mary J. Green, Darrah Haffner, Parthiv Haldipur, Suhair Hanna, Gunnar Houge, Jane Hurst, Cornelia Kraus, Birgit Elisabeth Kristiansen, James Lespinasse, Karen J. Low, Sally Ann Lynch, Sofia Maia, Rong Mao, Ruta Marcinkute, Catherine Melver, Kimberly McDonald, Tara Montgomery, Manuela Morleo, Constance Motter, Amanda S. Openshaw, Janice Cox Palumbos, Aditi Shah Parikh, Richard Person, Megha Desai, Juliette Piard, Rolph Pfundt, Marcello Scala, Margaux Serey-Gaut, Anne Slavotinek, Mohnish Suri, Claire Turner, Tatiana Tvrdik, Karin Weiss, Ingrid M. Wentzensen, Marcella Zollino, Bert B. A. de Vries, Francois Guillemot, William B. Dobyns, David Viskochil, Cristina Dias

المساهمون: A. Peron, F. D'Arco, K.A. Aldinger, C. Smith-Hick, C. Zweier, G.A. Gradek, K. Bradbury, A. Accogli, E.F. Andersen, P. Yee Billie Au, R. Battini, D. Beleford, L.M. Bird, A. Bouman, A. Bruel (O)yvind L(o)vold Busk, P.M. Campeau, V. Capra, C. Carlston, J. Carmichael, A. Chassevent, J. Clayton-Smith, M. J Bamshad, D.L. Earl, L. Faivre, C. Philippe, P. Ferrerira, L. Graul-Neumann, M.J. Green, D. Haffner, P. Haldipur, S. Hanna, G. Houge, J. Hurst, C. Krau, B. Elisabeth Kristiansen, J. Lespinasse, K.J. Low, S. Ann Lynch, S. Maia, R. Mao, R. Marcinkute, C. Melver, K. Mcdonald, T. Montgomery, M. Morleo, C. Motter, A.S. Openshaw, J. Cox Palumbo, A. Shah Parikh, R. Person, M. Desai, J. Piard, R. Pfundt, M. Scala, M. Serey-Gaut, A. Slavotinek, M. Suri, C. Turner, T. Tvrdik, K. Wei, I.M. Wentzensen, M. Zollino, B.B.A. de Vrie, F. Guillemot, W.B. Dobyn, D. Viskochil, C. Dias

مصطلحات موضوعية: BCL11A, rare disease, intellectual disability, neurodevelopmental disorder, fetal hemoglobin, cerebellar abnormalitie, microcephaly, Settore MED/03 - Genetica Medica

Relation: numberofpages:32; http://hdl.handle.net/2434/884476; https://www.medrxiv.org/content/10.1101/2021.09.06.21262776v1

الاتاحة: http://hdl.handle.net/2434/884476
https://doi.org/10.1101/2021.09.06.21262776
https://www.medrxiv.org/content/10.1101/2021.09.06.21262776v1

المؤلفون: Jie Xu, Kimberly Wallis, Sarah Ossler, Catherine Melver

المصدر: Cancer Genetics. :42-43

مصطلحات موضوعية: Cancer Research, Genetics, Molecular Biology

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::4adbafdd78d7e7b13c293691e3388ce8
https://doi.org/10.1016/j.cancergen.2022.10.136