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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, McDonald M, Campbell L, Ming JE, Zackai EH, Bejjani BA, Shaffer LG
Mol Cytogenet
2008,
1
:8
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PubMed Central articles that cite the above article:
1.
Molecular cytogenetics and cytogenomics of brain diseases.
Iourov IY, Vorsanova SG, Yurov YB
Curr Genomics
2008 Nov,
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Characterization of six human disease-associated inversion polymorphisms.
Antonacci F, Kidd JM, Marques-Bonet T, Ventura M, Siswara P, Jiang Z, Eichler EE
Hum Mol Genet
2009 Jul 15,
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