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Restriction Site-Specific Methylation Studies of Imprinted Genes with Quantitative Real-Time PCRBRUCE, Sara; HANNULA-JOUPPI, Katariina; LINDGREN, Cecilia M et al.Clinical chemistry (Baltimore, Md.). 2008, Vol 54, Num 3, pp 491-499, issn 0009-9147, 9 p.Article

Submicroscopic genomic alterations in Silver—Russell syndrome and Silver—Russell—like patientsBRUCE, Sara; HANNULA-JOUPPI, Katariina; PUOSKARI, Mari et al.Journal of medical genetics. 2010, Vol 47, Num 12, pp 816-822, issn 0022-2593, 7 p.Article

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Fine mapping of the 2p11 dyslexia locus and exclusion of TACR1 as a candidate genePEYRARD-JANVID, Myriam; ANTHONI, Heidi; KERE, Juha et al.Human genetics. 2004, Vol 114, Num 5, pp 510-516, issn 0340-6717, 7 p.Article

Absence of a paternally inherited FOXP2 gene in developmental verbal dyspraxiaFEUK, Lars; KALERVO, Aino; RIVLIN, Joseph et al.American journal of human genetics. 2006, Vol 79, Num 5, pp 965-972, issn 0002-9297, 8 p.Article

The mutation spectrum in RECQL4 diseasesSIITONEN, H. Annika; SOTKASIIRA, Jenni; KEYMOLEN, Kathelijn et al.European journal of human genetics. 2009, Vol 17, Num 2, pp 151-158, issn 1018-4813, 8 p.Article