L. Siggberg

Array CGH in molecular diagnosis of mental retardation—A study of 150 Finnish patients

S. Knuutila, S. Ala-Mello, L. Siggberg, 2010, American journal of medical genetics. Part A.

19p13.3 Aberrations Are Associated with Dysmorphic Features and Deviant Psychomotor Development

S. Knuutila, K. Näntö-Salonen, L. Siggberg, 2010, Cytogenetic and Genome Research.

9q22 Deletion - First Familial Case

S. Knuutila, Toshiyuki Yamamoto, L. Siggberg, 2011, Orphanet journal of rare diseases.

Further evidence for a relationship between the 5p15 chromosome region and the oculoauriculovertebral anomaly

S. Knuutila, H. von Koskull, L. Siggberg, 2008, American journal of medical genetics. Part A.

Potential role of a navigator gene NAV3 in colorectal cancer

S. Knuutila, K. Ovaska, S. Hautaniemi, 2011, British Journal of Cancer.

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

L. Siggberg, S. Janna, Ala-Mello Sirpa, 2012, BMC Medical Genetics.

Familial 6p22.2 duplication associates with mild developmental delay and increased SSADH activity

S. Knuutila, K. Gibson, C. Jakobs, 2011, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Further evidence for a relationship between the 5p15 chromosome region and the oculoauriculovertebral anomaly

S. Knuutila, H. von Koskull, L. Siggberg, 2008, American journal of medical genetics. Part A.