Showing results (1-10 of 66) with videos related to

Sort By:
Pageof 7
Methods in Molecular Biology (Clifton, N.J.)|March 19, 2010
Laboratory methods for the detection of chromosomal abnormalitiesJacqueline Schoumans, Claudia Ruivenkamp
European Journal of Medical Genetics|March 3, 2009
Detection of CHD7 deletions by MLPA in CHARGE syndrome patients with a less typical phenotypeJosephine Wincent, Astrid Schulze, Jacqueline Schoumans
European Journal of Medical Genetics|October 28, 2009
De novo deletion of chromosome 11q13.4-q14.3 in a boy with microcephaly, ptosis and developmental delayJosephine Wincent, Jacqueline Schoumans, Britt Marie Anderlid
Acta Haematologica|February 27, 2023
Description of an Institutional Cohort of Myeloid Neoplasms Carrying ETV6-Locus Deletions or ETV6 RearrangementsVasiliki Papadopoulou, Jacqueline Schoumans, Ilaria Scarpelli, et al.
American Journal of Medical Genetics. Part A|February 11, 2005
Detailed clinical description of four patients with 1.3 and 2.1 Mb chromosome imbalances derived from a familial t(12;17)(q24.33;q25.3)Jacqueline Schoumans, Gunnar Sanner, Magnus Nordenskjöld, et al.
Cells, Tissues, Organs|January 28, 2006
Long-term culture of human urothelial cells--a qualitative analysisMagdalena Fossum, Fredrik Lundberg, Kerstin Holmberg, et al.
BMC Research Notes|November 3, 2011
Mutation screening of patients with Alzheimer disease identifies APP locus duplication in a Swedish patientHåkan Thonberg, Marie Fallström, Jenny Björkström, et al.
European Journal of Medical Genetics|March 28, 2007
Duplication 16q12.1-q22.1 characterized by array CGH in a girl with spina bifidaPeter Gustavsson, Jacqueline Schoumans, Johan Staaf, et al.
Biomed Research International|April 16, 2015
Evolution of genetic techniques: past, present, and beyondAsude Alpman Durmaz, Emin Karaca, Urszula Demkow, et al.
Pageof 7