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Proceedings of the National Academy of Sciences of the United States of America|May 14, 2008

Common SNP in pre-miR-146a decreases mature miR expression and predisposes to papillary thyroid carcinomaKrystian Jazdzewski, Elizabeth L Murray, Kaarle Franssila, et al.

Spectrochimica Acta. Part A, Molecular and Biomolecular Spectroscopy|June 4, 2025

Conformational study of aptamer and its interaction with aflatoxin B1 using surface-enhanced Raman spectroscopyMarjan Majdinasab, Aicha Azziz, Gunnar Klös, et al.

International Journal of Cancer|February 20, 1991

Altered dosage of the sex chromosomes in human testicular cancer: a molecular genetic studyP Peltomäki, R Lothe, A L Børresen, et al.

Annals of Human Genetics|March 14, 2001

Skewed secondary sex ratio in the offspring of carriers of the 214G > A mutation of the RS1 geneL Huopaniemi, J Fellman, A Rantala, et al.

European Journal of Human Genetics : EJHG|July 1, 1997

Refined mapping of the Cohen syndrome gene by linkage disequilibriumJ Kolehmainen, R Norio, S Kivitie-Kallio, et al.

British Journal of Anaesthesia|March 20, 2003

Clonidine premedication improves metabolic control in type 2 diabetic patients during ophthalmic surgeryM Belhoula, J P Ciébiéra, A De La Chapelle, et al.

The American Journal of Pathology|August 6, 1999

Polymorphic variation at the BAT-25 and BAT-26 loci in individuals of African origin. Implications for microsatellite instability testingR Pyatt, R B Chadwick, C K Johnson, et al.

International Journal of Obstetric Anesthesia|January 26, 2006

Impact of walking epidural analgesia on obstetric outcome of nulliparous women in spontaneous labourA de la Chapelle, M Carles, V Gleize, et al.

Cancer Genetics and Cytogenetics|November 1, 1992

Chromosome 12 in human testicular cancer: dosage changes and their parental originP Peltomäki, R A Lothe, A L Børresen, et al.

Journal of Clinical Pathology|April 18, 2000

Danish type gelsolin related amyloidosis: 654G-T mutation is associated with a disease pathogenetically and clinically similar to that caused by the 654G-A mutation (familial amyloidosis of the Finnish type)C P Maury, M Liljeström, G Boysen, et al.

Pageof 61

Showing results (191-200 of 603) with videos related to

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Pageof 61

Proceedings of the National Academy of Sciences of the United States of America|May 14, 2008

Common SNP in pre-miR-146a decreases mature miR expression and predisposes to papillary thyroid carcinomaKrystian Jazdzewski, Elizabeth L Murray, Kaarle Franssila, et al.

Spectrochimica Acta. Part A, Molecular and Biomolecular Spectroscopy|June 4, 2025

Conformational study of aptamer and its interaction with aflatoxin B1 using surface-enhanced Raman spectroscopyMarjan Majdinasab, Aicha Azziz, Gunnar Klös, et al.

International Journal of Cancer|February 20, 1991

Altered dosage of the sex chromosomes in human testicular cancer: a molecular genetic studyP Peltomäki, R Lothe, A L Børresen, et al.

Annals of Human Genetics|March 14, 2001

Skewed secondary sex ratio in the offspring of carriers of the 214G > A mutation of the RS1 geneL Huopaniemi, J Fellman, A Rantala, et al.

European Journal of Human Genetics : EJHG|July 1, 1997

Refined mapping of the Cohen syndrome gene by linkage disequilibriumJ Kolehmainen, R Norio, S Kivitie-Kallio, et al.

British Journal of Anaesthesia|March 20, 2003

Clonidine premedication improves metabolic control in type 2 diabetic patients during ophthalmic surgeryM Belhoula, J P Ciébiéra, A De La Chapelle, et al.

The American Journal of Pathology|August 6, 1999

Polymorphic variation at the BAT-25 and BAT-26 loci in individuals of African origin. Implications for microsatellite instability testingR Pyatt, R B Chadwick, C K Johnson, et al.

International Journal of Obstetric Anesthesia|January 26, 2006

Impact of walking epidural analgesia on obstetric outcome of nulliparous women in spontaneous labourA de la Chapelle, M Carles, V Gleize, et al.

Cancer Genetics and Cytogenetics|November 1, 1992

Chromosome 12 in human testicular cancer: dosage changes and their parental originP Peltomäki, R A Lothe, A L Børresen, et al.

Journal of Clinical Pathology|April 18, 2000

Danish type gelsolin related amyloidosis: 654G-T mutation is associated with a disease pathogenetically and clinically similar to that caused by the 654G-A mutation (familial amyloidosis of the Finnish type)C P Maury, M Liljeström, G Boysen, et al.

Pageof 61