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Journal of Neuroendocrinology|July 11, 2012
Locked nucleic acid-based in situ hybridisation reveals miR-7a as a hypothalamus-enriched microRNA with a distinct expression patternS Herzer, A Silahtaroglu, B MeisterCytogenetic and Genome Research|August 12, 2004
LNA-modified oligonucleotides are highly efficient as FISH probesA Silahtaroglu, H Pfundheller, A Koshkin, et al.Genetic Counseling (Geneva, Switzerland)|January 5, 2001
Two cases of partial trisomy 10q syndrome due to a familial 10;20 translocationB Tüysüz, S Hacihanefioglu, A Silahtaroglu, et al.European Journal of Human Genetics : EJHG|April 21, 2001
MECP2 mutations in Danish patients with Rett syndrome: high frequency of mutations but no consistent correlations with clinical severity or with the X chromosome inactivation patternJ B Nielsen, K F Henriksen, C Hansen, et al.Clinical Genetics|June 22, 2010
RUNX2 analysis of Danish cleidocranial dysplasia familiesL Hansen, A K Riis, A Silahtaroglu, et al.Blood|June 20, 1998
The human intrinsic factor-vitamin B12 receptor, cubilin: molecular characterization and chromosomal mapping of the gene to 10p within the autosomal recessive megaloblastic anemia (MGA1) regionR Kozyraki, M Kristiansen, A Silahtaroglu, et al.The American Journal of Physiology|September 9, 1998
Characterization of the cloned human intermediate-conductance Ca2+-activated K+ channelB S Jensen, D Strobaek, P Christophersen, et al.Journal of Medical Genetics|June 28, 2005
Breakpoints around the HOXD cluster result in various limb malformationsB Dlugaszewska, A Silahtaroglu, C Menzel, et al.European Journal of Human Genetics : EJHG|March 27, 1999
Molecular cytogenetic detection of 9q34 breakpoints associated with nail patella syndromeA Silahtaroglu, F A Hol, P K Jensen, et al.Pageof 1