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6. Detection of genomic imbalances by array based comparative genomic hybridisation in fetuses with multiple malformations. Le Caignec C; Boceno M; Saugier-Veber P; Jacquemont S; Joubert M; David A; Frebourg T; Rival JM J Med Genet; 2005 Feb; 42(2):121-8. PubMed ID: 15689449 [TBL] [Abstract][Full Text] [Related]
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13. [Detection and related analysis to chromosome 22q11 microdeletion in patients with congenital heart diseases]. Xu ZF; Yi L; Mo XM; Hu Y; Wang DJ; Zhu RF; Jiang YZ; Wu X; Wu Z; Shen L; Zhang Y; Zhong XL Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2006 Jun; 23(3):250-5. PubMed ID: 16767657 [TBL] [Abstract][Full Text] [Related]
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20. Chromosomal rearrangements in children with idiopathic mental retardation using subtelomeric fluorescent in situ hybridization. Cogulu O; Gunduz C; Karaca E; Onay H; Ozkinay C; Ozkinay F Genet Couns; 2006; 17(3):321-31. PubMed ID: 17100201 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]