Mild Wolf-Hirschhorn syndrome: micro-array CGH analysis of atypical 4p16.3 deletions enables refinement of the genotype-phenotype map. Issue 9 (1st September 2004)

• Record Type: Journal Article
• Authors: Van Buggenhout, G; Melotte, C; Dutta, B; Froyen, G; Van Hummelen, P; Marynen, P; Matthijs, G; de Ravel, T; Devriendt, K; Fryns, J P; Vermeesch, J R
• Is Part Of: Journal of medical genetics. Volume 41:Issue 9(2004)
• Page Start: 691
• Page End: 698
• Publication Date: 2004-09-01
• Subjects: array CGH, micro-array CGH -- DOP PCR, degenerate oligonucleotide primed PCR -- FISH, fluorescence in situ hybridisation -- LETM1, a calcium channel gene -- log2 IR, log2 of the intensity ratio -- ORGC, olfactory receptor gene cluster -- WHSC1, Wolf-Hirschhorn Syndrome Candidate gene 1 -- WHSC2, Wolf-Hirschhorn Syndrome Candidate gene 2 -- WHSCR1, Wolf-Hirschhorn critical region 1 -- WHSCR2, Wolf-Hirschhorn critical region 2; 4p deletion syndrome -- array CGH -- olfactory receptor gene cluster -- WHSC1 -- Wolf-Hirschhorn syndrome; Medical genetics -- Periodicals; 616.042
• DOI: 10.1136/jmg.2003.016865
• Languages: English
• ISSNs: 1468-6244