Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Gannaway, Rachel"'
Autor:
Castilla-Vallmanya, Laura, Selmer, Kaja K., Dimartino, Clémantine, Rabionet, Raquel, Blanco-Sánchez, Bernardo, Yang, Sandra, Reijnders, Margot R.F., van Essen, Antonie J., Oufadem, Myriam, Vigeland, Magnus D., Stadheim, Barbro, Houge, Gunnar, Cox, Helen, Kingston, Helen, Clayton-Smith, Jill, Innis, Jeffrey W., Iascone, Maria, Cereda, Anna, Gabbiadini, Sara, Chung, Wendy K., Sanders, Victoria, Charrow, Joel, Bryant, Emily, Millichap, John, Vitobello, Antonio, Thauvin, Christel, Mau-Them, Frederic Tran, Faivre, Laurence, Lesca, Gaetan, Labalme, Audrey, Rougeot, Christelle, Chatron, Nicolas, Sanlaville, Damien, Christensen, Katherine M., Kirby, Amelia, Lewandowski, Raymond, Gannaway, Rachel, Aly, Maha, Lehman, Anna, Clarke, Lorne, Graul-Neumann, Luitgard, Zweier, Christiane, Lessel, Davor, Lozic, Bernarda, Aukrust, Ingvild, Peretz, Ryan, Stratton, Robert, Smol, Thomas, Dieux-Coëslier, Anne, Meira, Joanna, Wohler, Elizabeth, Sobreira, Nara, Beaver, Erin M., Heeley, Jennifer, Briere, Lauren C., High, Frances A., Sweetser, David A., Walker, Melissa A., Keegan, Catherine E., Jayakar, Parul, Shinawi, Marwan, Kerstjens-Frederikse, Wilhelmina S., Earl, Dawn L., Siu, Victoria M., Reesor, Emma, Yao, Tony, Hegele, Robert A., Vaske, Olena M., Rego, Shannon, Shapiro, Kevin A., Wong, Brian, Gambello, Michael J., McDonald, Marie, Karlowicz, Danielle, Colombo, Roberto, Serretti, Alessandro, Pais, Lynn, O’Donnell-Luria, Anne, Wray, Alison, Sadedin, Simon, Chong, Belinda, Tan, Tiong Y., Christodoulou, John, White, Susan M., Slavotinek, Anne, Barbouth, Deborah, Morel Swols, Dayna, Parisot, Mélanie, Bole-Feysot, Christine, Nitschké, Patrick, Pingault, Véronique, Munnich, Arnold, Cho, Megan T., Cormier-Daire, Valérie, Balcells, Susanna, Lyonnet, Stanislas, Grinberg, Daniel, Amiel, Jeanne, Urreizti, Roser, Gordon, Christopher T.
Publikováno v:
In Genetics in Medicine July 2020 22(7):1215-1226
Autor:
Choi, Jamie H., Li, Rachel, Gannaway, Rachel, Causey, Tahnee N., Harrison, Anna, Couser, Natario L.
Publikováno v:
Case Reports in Genetics.
Shprintzen–Goldberg craniosynostosis syndrome (SGS) is a rare autosomal dominant condition that was first documented in literature in 1982. The disorder is caused by pathogenic variants in the proto-oncogene SKI gene, a known suppressor of TGF-β a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=hindawi_publ::9cb0c3ba2d03fd85582c79e2c21aa547
Publikováno v:
In Fertility and Sterility September 2019 112(3) Supplement:e352-e352
Autor:
Choi, Jamie H., Li, Rachel, Gannaway, Rachel, Causey, Tahnee N., Harrison, Anna, Couser, Natario L.
Publikováno v:
Case Reports in Genetics; 8/31/2021, p1-2, 2p
Publikováno v:
Journal of Speech, Language & Hearing Research; Feb2005, Vol. 48 Issue 1, p137-156, 20p, 2 Diagrams, 4 Charts, 3 Graphs
Autor:
Choi, Jamie H., Li, Rachel, Gannaway, Rachel, Causey, Tahnee N., Harrison, Anna, Couser, Natario L.
Publikováno v:
Case Reports in Genetics; 11/16/2020, p1-1, 1p
Autor:
H. Choi, Jamie, Li, Rachel, Gannaway, Rachel, N. Causey, Tahnee, Harrison, Anna, L. Couser, Natario
Publikováno v:
Case Reports in Genetics; 2021, Vol. 2021 Issue: 1
Autor:
H. Choi, Jamie, Li, Rachel, Gannaway, Rachel, N. Causey, Tahnee, Harrison, Anna, L. Couser, Natario
Publikováno v:
Case Reports in Genetics; 2020, Vol. 2020 Issue: 1
Autor:
H. Choi, Jamie, Li, Rachel, Gannaway, Rachel, N. Causey, Tahnee, Harrison, Anna, L. Couser, Natario
Publikováno v:
Case Reports in Genetics; 2020, Vol. 2020 Issue: 1
Publikováno v:
Cleft Palate Craniofacial Journal; 2019 Supplement 1, Vol. 56, p140-160, 21p