A. Björkqvist

发表

DNA copy number amplifications in human neoplasms: review of comparative genomic hybridization studies.

S. Knuutila, O. Monni, M. Wolf, 1998, The American journal of pathology.

A broad amplification pattern at 3q in squamous cell lung cancer--a fluorescence in situ hybridization study.

S. Knuutila, S. Anttila, K. Husgafvel‐Pursiainen, 2000, Cancer genetics and cytogenetics.

DNA copy number losses in human neoplasms.

K Autio, S. Knuutila, O. Monni, 1999, The American journal of pathology.

Optimization of comparative genomic hybridization using fluorochrome conjugated to dCTP and dUTP nucleotides.

S. Knuutila, M. Larramendy, A. Björkqvist, 1997, Laboratory investigation; a journal of technical methods and pathology.

Localization of a susceptibility locus for Peutz-Jeghers syndrome to 19p using comparative genomic hybridization and targeted linkage analysis

Darryl Shibata, Ian Tomlinson, Sakari Knuutila, 1997, Nature Genetics.

Deletions at 14q in malignant mesothelioma detected by microsatellite marker analysis

J. Kere, S. Knuutila, M. Wolf, 1999, British Journal of Cancer.

Recurrent DNA copy number changes in 1q, 4q, 6q, 9p, 13q, 14q and 22q detected by comparative genomic hybridization in malignant mesothelioma.

S. Knuutila, S. Anttila, A. Björkqvist, 1997, British Journal of Cancer.

Gains and losses of DNA sequences in malignant mesothelioma by comparative genomic hybridization.

K. Pelin, O. Kallioniemi, S. Knuutila, 1996, Cancer genetics and cytogenetics.

DNA gains in 3q occur frequently in squamous cell carcinoma of the lung, but not in adenocarcinoma

S. Knuutila, S. Anttila, K. Husgafvel‐Pursiainen, 1998, Genes, chromosomes & cancer.

Comparative genomic hybridization reveals complex genetic changes in primary breast cancer tumors and their cell lines.

I. Wistuba, A. Gazdar, S. Knuutila, 2000, Cancer genetics and cytogenetics.

Comparative genomic hybridization study on pooled DNAs from tumors of one clinical-pathological entity.

S. Knuutila, O. Monni, G. Armengol, 1998, Cancer genetics and cytogenetics.

Absence of trisomy 7 in nonneoplastic human ascitic and pleural fluid cells. An interphase cytogenetic study.

S. Knuutila, M. Larramendy, A. Björkqvist, 1994, Cancer genetics and cytogenetics.

Prenatal sex determination by in situ hybridization on fetal nucleated cells in maternal whole venous blood

S. Knuutila, M. Wessman, A. Björkqvist, 1994, Clinical genetics.