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Autor:
Martha E. Lopez-Burks, Shimako Kawauchi, Arthur D. Lander, Rosaysela Santos, Akihiko Muto, Anne L. Calof, Thomas F. Schilling
Publikováno v:
American journal of medical genetics. Part C, Seminars in medical genetics, vol 172, iss 2
Kawauchi, S; Santos, R; Muto, A; Lopez-Burks, ME; Schilling, TF; Lander, AD; et al.(2016). Using Mouse and Zebrafish Models to Understand the Etiology of Developmental Defects in Cornelia de Lange Syndrome. AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS, 172(2), 138-145. doi: 10.1002/ajmg.c.31484. UC Irvine: Retrieved from: http://www.escholarship.org/uc/item/1kn4m2w9
Kawauchi, S; Santos, R; Muto, A; Lopez-Burks, ME; Schilling, TF; Lander, AD; et al.(2016). Using Mouse and Zebrafish Models to Understand the Etiology of Developmental Defects in Cornelia de Lange Syndrome. AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS, 172(2), 138-145. doi: 10.1002/ajmg.c.31484. UC Irvine: Retrieved from: http://www.escholarship.org/uc/item/1kn4m2w9
Cornelia de Lange Syndrome (CdLS) is a multisystem birth defects disorder that affects every tissue and organ system in the body. Understanding the factors that contribute to the origins, prevalence, and severity of these developmental defects provid