High-resolution SNP array analysis of patients with developmental disorder and normal array CGH result (vol 13, 84, 2012)

Autor: Siggberg, Linda, Ala-Mello, Sirpa, Linnankivi, Tarja, Avela, Kristiina, Scheinin, Ilari, Kristiansson, Kati, Lahermo, Paivi, Hietala, Marja, Metsähonkala, Liisa, Kuusinen, Esa, Laaksonen, Maarit, Saarela, Janna, Knuutila, Sakari

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______1593::a5b22416ee6a052505c906a2e0eafd38
http://hdl.handle.net/10138/164111

High-resolution SNP array analysis of patients with developmental disorder and normal array CGH results

Autor: Ala-Mello Sirpa, Lahermo Paivi, Avela Kristiina, Linnankivi Tarja, Kuusinen Esa, Linda Siggberg, Metsahonkala Liisa, Kristiansson Kati, Hietala Marja, Laaksonen Maarit, Saarela Janna, Knuutila Sakari, Scheinin Ilari

Publikováno v: BMC Medical Genetics, Vol 13, Iss 1, p 84 (2012)
BMC Medical Genetics, 13:84. BioMed Central
BMC Medical Genetics
Siggberg, L, Alla-Melo, S, Linnankivi, T, Avela, K, Scheinin, A I, Kristiansson, K, Lahermo, P, Hietala, M, Metsähonkala, L, Kuusinen, E, Laaksonen, M, Saarela, J & Knuutila, S 2012, ' High-resolution SNP array analysis of patients with developmental disorder and normal array CGH results ', BMC Medical Genetics, vol. 13, 84 . https://doi.org/10.1186/1471-2350-13-84

Background Diagnostic analysis of patients with developmental disorders has improved over recent years largely due to the use of microarray technology. Array methods that facilitate copy number analysis have enabled the diagnosis of up to 20% more pa

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::653fe1c8c62af06707bc64f402c84176

High-resolution SNP array analysis of patients with developmental disorder and normal array CGH results.

Autor: Siggberg L; Department of Pathology, Haartman Institute, University of Helsinki, Finland. linda.siggberg@helsinki.fi, 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

Publikováno v: BMC medical genetics [BMC Med Genet] 2012 Sep 17; Vol. 13, pp. 84. Date of Electronic Publication: 2012 Sep 17.