Publications by authors named "April Hacker"

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Analysis of the t(3;8) of hereditary renal cell carcinoma: a palindrome-mediated translocation.
Takema Kato, Colleen P Franconi, Molly B Sheridan, April M Hacker, Hidehito Inagakai

Cancer Genet· April 2014

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A palindrome-mediated recurrent translocation with 3:1 meiotic nondisjunction: the t(8;22)(q24.13;q11.21).
Molly B Sheridan, Takema Kato, Chad Haldeman-Englert, G Reza Jalali, Jeff M Milunsky, April M Hacker

Am J Hum Genet· August 2010

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Interrupted aortic arch type B in A patient with cat eye syndrome.
Sintia Iole Nogueira Belangero, Fernanda Teixeira da Silva Bellucco, Mirlene C S P Cernach, April M Hacker, Beverly S Emanuel

Arq Bras Cardiol· May 2009

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Atypical 22q11.2 deletion in a patient with DGS/VCFS spectrum.
Sintia Iole Nogueira, April M Hacker, Fernanda T S Bellucco, Denise M Christofolini, Leslie Domenici Kulikowski

Eur J Med Genet· August 2008

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Deletion 22q11.2: report of a complex meiotic mechanism of origin.
Sintia Iole Nogueira, April M Hacker, Fernanda T S Bellucco, Leslie Domenici Kulikowski, Denise Maria Christofolini

Am J Med Genet A· August 2007

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A palindrome-driven complex rearrangement of 22q11.2 and 8q24.1 elucidated using novel technologies.
Anthony L Gotter, Manjunath A Nimmakayalu, G Reza Jalali, April M Hacker, Jacob Vorstman

Genome Res· April 2007

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Low copy repeats mediate distal chromosome 22q11.2 deletions: sequence analysis predicts breakpoint mechanisms.
Tamim H Shaikh, Ronald J O'Connor, Mary Ella Pierpont, James McGrath, April M Hacker

Genome Res· April 2007

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High-resolution mapping of DNA copy alterations in human chromosome 22 using high-density tiling oligonucleotide arrays.
Alexander Eckehart Urban, Jan O Korbel, Rebecca Selzer, Todd Richmond, April Hacker

Proc Natl Acad Sci U S A· March 2006

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A unique case of der(11)t(11;22),-22 arising from 3:1 segregation of a maternal t(11;22) in a family with co-segregation of the translocation and breast cancer.
Vaidehi Jobanputra, Wendy K Chung, April M Hacker, Beverly S Emanuel, Dorothy Warburton

Prenat Diagn· August 2005

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Aberrant interchromosomal exchanges are the predominant cause of the 22q11.2 deletion.
Sulagna C Saitta, Stacy E Harris, Ann P Gaeth, Deborah A Driscoll, Donna M McDonald-McGinn, April M Hacker

Hum Mol Genet· February 2004

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