Victoria B. Enciso

Microduplications of 22q11.2 are frequently inherited and are associated with variable phenotypes

Zhishuo Ou, Jonathan S. Berg, Hagith Yonath et al. · Genetics in Medicine · 2008 · 223 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Observation and prediction of recurrent human translocations mediated by NAHR between nonhomologous chromosomes

Zhishuo Ou, Paweł Stankiewicz, Zhilian Xia et al. · Genome Research · 2011 · 95 citations · Full text

Life Sciences, Genetics, Molecular Genetics +15

Chromosomal microarray analysis (CMA) detects a large X chromosome deletion including <i>FMR1</i>, <i>FMR2</i>, and <i>IDS</i> in a female patient with mental retardation

Frank J. Probst, Elizabeth Roeder, Victoria B. Enciso et al. · American Journal of Medical Genetics Part A · 2007 · 60 citations

Life Sciences, Genetics, Molecular Genetics +17

Identification of proximal 1p36 deletions using array‐CGH: a possible new syndrome

S‐HL Kang, A. Scheffer, Zhishuo Ou et al. · Clinical Genetics · 2007 · 57 citations

Life Sciences, Genetics, Molecular Genetics +17

Recurrent microdeletions of 15q25.2 are associated with increased risk of congenital diaphragmatic hernia, cognitive deficits and possibly Diamond–Blackfan anaemia

Margaret Wat, Victoria B. Enciso, Wojciech Wiszniewski et al. · Journal of Medical Genetics · 2010 · 44 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17