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9q22 Deletion--first familial case.
Orphanet J Rare Dis. 2011 Jun 22;6:45. doi: 10.1186/1750-1172-6-45.
Orphanet J Rare Dis. 2011.
PMID: 21693067
Free PMC article.
19p13.3 aberrations are associated with dysmorphic features and deviant psychomotor development.
Siggberg L, Olsén P, Näntö-Salonen K, Knuutila S.
Siggberg L, et al.
Cytogenet Genome Res. 2011;132(1-2):8-15. doi: 10.1159/000320920. Epub 2010 Oct 8.
Cytogenet Genome Res. 2011.
PMID: 20938164
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Array CGH in molecular diagnosis of mental retardation - A study of 150 Finnish patients.
Siggberg L, Ala-Mello S, Jaakkola E, Kuusinen E, Schuit R, Kohlhase J, Böhm D, Ignatius J, Knuutila S.
Siggberg L, et al.
Am J Med Genet A. 2010 Jun;152A(6):1398-410. doi: 10.1002/ajmg.a.33402.
Am J Med Genet A. 2010.
PMID: 20503314
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Familial 6p22.2 duplication associates with mild developmental delay and increased SSADH activity.
Siggberg L, Mustonen A, Schuit R, Salomons GS, Roos B, Gibson KM, Jakobs C, Ignatius J, Knuutila S.
Siggberg L, et al.
Am J Med Genet B Neuropsychiatr Genet. 2011 Jun;156B(4):448-53. doi: 10.1002/ajmg.b.31180. Epub 2011 Mar 22.
Am J Med Genet B Neuropsychiatr Genet. 2011.
PMID: 21438145
Free PMC article.
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Further evidence for a relationship between the 5p15 chromosome region and the oculoauriculovertebral anomaly.
Ala-Mello S, Siggberg L, Knuutila S, von Koskull H, Taskinen M, Peippo M.
Ala-Mello S, et al. Among authors: siggberg l.
Am J Med Genet A. 2008 Oct 1;146A(19):2490-4. doi: 10.1002/ajmg.a.32479.
Am J Med Genet A. 2008.
PMID: 18792983
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Potential role of a navigator gene NAV3 in colorectal cancer.
Carlsson E, Ranki A, Sipilä L, Karenko L, Abdel-Rahman WM, Ovaska K, Siggberg L, Aapola U, Ässämäki R, Häyry V, Niiranen K, Helle M, Knuutila S, Hautaniemi S, Peltomäki P, Krohn K.
Carlsson E, et al. Among authors: siggberg l.
Br J Cancer. 2012 Jan 31;106(3):517-24. doi: 10.1038/bjc.2011.553. Epub 2011 Dec 15.
Br J Cancer. 2012.
PMID: 22173670
Free PMC article.
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Erratum to: High-resolution SNP array analysis of patients with developmental disorder and normal array CGH result.
Siggberg L, Ala-Mello S, Linnankivi T, Avela K, Scheinin I, Kristiansson K, Lahermo P, Hietala M, Metsähonkala L, Kuusinen E, Laaksonen M, Saarela J, Knuutila S.
Siggberg L, et al.
BMC Med Genet. 2014 Nov 18;15:124. doi: 10.1186/s12881-014-0124-3.
BMC Med Genet. 2014.
PMID: 25928284
Free PMC article.
No abstract available.
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High-resolution SNP array analysis of patients with developmental disorder and normal array CGH results.
Siggberg L, Ala-Mello S, Linnankivi T, Avela K, Scheinin I, Kristiansson K, Lahermo P, Hietala M, Metsähonkala L, Kuusinen E, Laaksonen M, Saarela J, Khuutila S.
Siggberg L, et al.
BMC Med Genet. 2012 Sep 17;13:84. doi: 10.1186/1471-2350-13-84.
BMC Med Genet. 2012.
PMID: 22984989
Free PMC article.
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