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P Paavola

Showing results (1-10 of 25) with videos related to

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Journal of Medical Genetics|June 27, 1998
Meckel syndromeR Salonen, P Paavola
Clinical Otolaryngology : Official Journal of ENT-UK ; Official Journal of Netherlands Society for Oto-Rhino-Laryngology & Cervico-Facial Surgery|May 27, 2010
Standardised photographic documentation of the auricleA A Mäkitie, P Paavola, T Klockars
Nature Genetics|October 1, 1995
The locus for Meckel syndrome with multiple congenital anomalies maps to chromosome 17q21-q24P Paavola, R Salonen, J Weissenbach, et al.
Genomics|January 16, 1999
Characterization of a novel gene, PNUTL2, on human chromosome 17q22-q23 and its exclusion as the Meckel syndrome geneP Paavola, N Horelli-Kuitunen, A Palotie, et al.
Psychological Medicine|July 21, 2004
Characteristics and circumstances of homicidal acts committed by offenders with schizophreniaC C Joyal, A Putkonen, P Paavola, et al.
American Journal of Human Genetics|September 16, 1999
Assignment of the locus for hydrolethalus syndrome to a highly restricted region on 11q23-25I Visapää, R Salonen, T Varilo, et al.
Duodecim; Laaketieteellinen Aikakauskirja|June 25, 2002
[What is known about genetic factors behind chronic inflammatory bowel diseases?]T Heliö, P Paavola, L Halme, et al.
Radiotherapy and Oncology : Journal of the European Society for Therapeutic Radiology and Oncology|May 15, 2018
Overall survival after stereotactic radiotherapy or surgical metastasectomy in oligometastatic renal cell carcinoma patients treated at two Swedish centres 2005-2014M Stenman, G Sinclair, P Paavola, et al.
Acta Orthopaedica|January 18, 2012
Operative and nonoperative treatment of clavicle fractures in adultsKaisa J Virtanen, Antti O V Malmivaara, Ville M Remes, et al.
Clinical Dysmorphology|July 1, 1997
Exclusion of the p75 neurotrophin receptor gene as a candidate gene for Meckel syndromeK Wartiovaara, P Paavola, P Suvanto, et al.
Pageof 3

Showing results (1-10 of 25) with videos related to

Sort By:
Pageof 3
Journal of Medical Genetics|June 27, 1998
Meckel syndromeR Salonen, P Paavola
Clinical Otolaryngology : Official Journal of ENT-UK ; Official Journal of Netherlands Society for Oto-Rhino-Laryngology & Cervico-Facial Surgery|May 27, 2010
Standardised photographic documentation of the auricleA A Mäkitie, P Paavola, T Klockars
Nature Genetics|October 1, 1995
The locus for Meckel syndrome with multiple congenital anomalies maps to chromosome 17q21-q24P Paavola, R Salonen, J Weissenbach, et al.
Genomics|January 16, 1999
Characterization of a novel gene, PNUTL2, on human chromosome 17q22-q23 and its exclusion as the Meckel syndrome geneP Paavola, N Horelli-Kuitunen, A Palotie, et al.
Psychological Medicine|July 21, 2004
Characteristics and circumstances of homicidal acts committed by offenders with schizophreniaC C Joyal, A Putkonen, P Paavola, et al.
American Journal of Human Genetics|September 16, 1999
Assignment of the locus for hydrolethalus syndrome to a highly restricted region on 11q23-25I Visapää, R Salonen, T Varilo, et al.
Duodecim; Laaketieteellinen Aikakauskirja|June 25, 2002
[What is known about genetic factors behind chronic inflammatory bowel diseases?]T Heliö, P Paavola, L Halme, et al.
Radiotherapy and Oncology : Journal of the European Society for Therapeutic Radiology and Oncology|May 15, 2018
Overall survival after stereotactic radiotherapy or surgical metastasectomy in oligometastatic renal cell carcinoma patients treated at two Swedish centres 2005-2014M Stenman, G Sinclair, P Paavola, et al.
Acta Orthopaedica|January 18, 2012
Operative and nonoperative treatment of clavicle fractures in adultsKaisa J Virtanen, Antti O V Malmivaara, Ville M Remes, et al.
Clinical Dysmorphology|July 1, 1997
Exclusion of the p75 neurotrophin receptor gene as a candidate gene for Meckel syndromeK Wartiovaara, P Paavola, P Suvanto, et al.
Pageof 3