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Expanding the clinical phenotype of the 3q29 microdeletion syndrome and characterization of the reciprocal microduplication.
Ballif BC, Theisen A, Coppinger J, Gowans GC, Hersh JH, Madan-Khetarpal S, Schmidt KR, Tervo R, Escobar LF, Friedrich CA, et al.
Mol Cytogenet. 2008 Apr 28; 1:8. Epub 2008 Apr 28.
[Mol Cytogenet. 2008]
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Clinical implementation of chromosomal microarray analysis: summary of 2513 postnatal cases.
Lu X, Shaw CA, Patel A, Li J, Cooper ML, Wells WR, Sullivan CM, Sahoo T, Yatsenko SA, Bacino CA, et al.
PLoS One. 2007 Mar 28; 2(3):e327. Epub 2007 Mar 28.
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Genetic proof of unequal meiotic crossovers in reciprocal deletion and duplication of 17p11.2.
Shaw CJ, Bi W, Lupski JR.
Am J Hum Genet. 2002 Nov; 71(5):1072-81. Epub 2002 Oct 9.
[Am J Hum Genet. 2002]
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