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Methods in Molecular Biology (Clifton, N.J.)|March 19, 2010
Laboratory methods for the detection of chromosomal abnormalitiesJacqueline Schoumans, Claudia Ruivenkamp
Oncogene|May 31, 2003
LOH of PTPRJ occurs early in colorectal cancer and is associated with chromosomal loss of 18q12-21Claudia Ruivenkamp, Mario Hermsen, Cindy Postma, et al.
Human Genetics|September 1, 2005
Analysis of missense variants in the PKHD1-gene in patients with autosomal recessive polycystic kidney disease (ARPKD)Monique Losekoot, Cathleen Haarloo, Claudia Ruivenkamp, et al.
American Journal of Medical Genetics. Part A|March 20, 2025
Proximal Deletions of 14q32.2 Result in Severe Neurodevelopmental Outcomes, Congenital Anomalies, and Dysmorphic FeaturesJennifer Black, Robert Roger Lebel, Ria Garg, et al.
American Journal of Medical Genetics. Part A|April 9, 2009
Split hand-foot malformation, tetralogy of Fallot, mental retardation and a 1 Mb 19p deletion-evidence for further heterogeneity?Emmelien Aten, Nicolette den Hollander, Claudia Ruivenkamp, et al.
Hormone Research in Paediatrics|March 11, 2010
Genome-wide SNP array analysis in patients with features of sotos syndromeRemco Visser, Antoinet Gijsbers, Claudia Ruivenkamp, et al.
European Journal of Human Genetics : EJHG|October 21, 2004
Genome-wide screening using array-CGH does not reveal microdeletions/microduplications in children with Kabuki syndromeJacqueline Schoumans, Ann Nordgren, Claudia Ruivenkamp, et al.
European Journal of Medical Genetics|April 14, 2009
Array analysis and karyotyping: workflow consequences based on a retrospective study of 36,325 patients with idiopathic developmental delay in the NetherlandsRon Hochstenbach, Ellen van Binsbergen, John Engelen, et al.
European Journal of Human Genetics : EJHG|February 21, 2008
Detection of submicroscopic constitutional chromosome aberrations in clinical diagnostics: a validation of the practical performance of different array platformsZhong-Fa Zhang, Claudia Ruivenkamp, Johan Staaf, et al.
Breast Cancer Research and Treatment|February 12, 2009
A 7 Mb region within 11q13 may contain a high penetrance gene for breast cancerJuan Manuel Rosa-Rosa, Guillermo Pita, Anna González-Neira, et al.
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