Mutations in GDF11 and the extracellular antagonist, Follistatin, as a likely cause of Mendelian forms of orofacial clefting in humans.
Cox, Timothy C; Lidral, Andrew C; McCoy, Jason C; Liu, Huan; Cox, Liza L; Zhu, Ying; Anderson, Ryan D; Moreno Uribe, Lina M; Anand, Deepti; Deng, Mei; Richter, Chika T; Nidey, Nichole L; Standley, Jennifer M; Blue, Elizabeth E; Chong, Jessica X; Smith, Joshua D; Kirk, Edwin P; Venselaar, Hanka; Krahn, Katy N; van Bokhoven, Hans; Zhou, Huiqing; Cornell, Robert A; Glass, Ian A; Bamshad, Michael J; Nickerson, Deborah A; Murray, Jeffrey C; Lachke, Salil A; Thompson, Thomas B; Buckley, Michael F; Roscioli, Tony.
; 40(10): 1813-1825, 2019 10.
Artigo em Inglês | MEDLINE | ID: mdl-31215115
Exome Sequencing Discerns Syndromes in Patients from Consanguineous Families with Congenital Anomalies of the Kidneys and Urinary Tract.
[Detection and functional analysis of BMP2 gene mutation in patients with tooth agenesis].
Nonlinear effects in evolution - an ab initio study: A model in which the classical theory of evolution occurs as a special case.