S. Yu

Fragile X syndrome without CCG amplification has an FMR1 deletion

Ági K. Gedeon, Emma K. Baker, Harriet L. Robinson et al. · Nature Genetics · 1992 · 218 citations

Mendelian Disorder, Genetic Disorder, Genetics +8

Refining the 22q11.2 deletion breakpoints in DiGeorge syndrome by aCGH

Douglas C. Bittel, S. Yu, Heather L. Newkirk et al. · Cytogenetic and Genome Research · 2009 · 66 citations · Full text

Cytogenetics, Genetics, Distal Lcr +18

Localisation of a 10q breakpoint within the PAX2 gene in a patient with a de novo t(10;13) translocation and optic nerve coloboma-renal disease.

Kouji Narahara, E Baker, Sakiko Ito et al. · Journal of Medical Genetics · 1997 · 48 citations · Full text

Telomere Capture as a Frequent Mechanism for Stabilization of the Terminal Chromosomal Deletion Associated with Inverted Duplication

S. Yu, W. Graf · Cytogenetic and Genome Research · 2010 · 45 citations

Chromatin, Genome Instability, Chromosome Dynamics +15

Characterizing Small Supernumerary Marker Chromosomes with Combination of Multiple Techniques

S. Yu, Stephanie D. Fiedler, S.J. Brawner et al. · Cytogenetic and Genome Research · 2011 · 22 citations

Genetic Testing, Cytogenetics, Genetics +22