Publications by authors named "Victoria Enciso"

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Metastatic medulloblastoma in an adolescent with Simpson-Golabi-Behmel syndrome.
Martha Thomas, Victoria Enciso, Robert Stratton, Shafqat Shah, Thomas Winder

Am J Med Genet A· October 2012

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Observation and prediction of recurrent human translocations mediated by NAHR between nonhomologous chromosomes.
Zhishuo Ou, Paweł Stankiewicz, Zhilian Xia, Amy M Breman, Brian Dawson, Victoria B Enciso

Genome Res· January 2011

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Recurrent microdeletions of 15q25.2 are associated with increased risk of congenital diaphragmatic hernia, cognitive deficits and possibly Diamond--Blackfan anaemia.
Margaret J Wat, Victoria B Enciso, Wojciech Wiszniewski, Trevor Resnick, Patricia Bader

J Med Genet· November 2010

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Microduplications of 22q11.2 are frequently inherited and are associated with variable phenotypes.
Zhishuo Ou, Jonathan S Berg, Hagith Yonath, Victoria B Enciso, David T Miller

Genet Med· April 2008

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Chromosomal microarray analysis (CMA) detects a large X chromosome deletion including FMR1, FMR2, and IDS in a female patient with mental retardation.
Frank J Probst, Elizabeth R Roeder, Victoria B Enciso, Zhishuo Ou, M Lance Cooper

Am J Med Genet A· June 2007

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