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T Martinsson

Showing results (111-120 of 146) with videos related to

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Hereditas|January 1, 1987
Isolation of selectively amplified DNA sequences from multidrug-resistant SEWA cellsF Stähl, P Sandberg, T Martinsson, et al.
Archives of Dermatological Research|February 24, 2001
Stronger association with HLA-Cw6 than with corneodesmosin (S-gene) polymorphisms in Swedish psoriasis patientsC Enerbäck, S Nilsson, F Enlund, et al.
Human Mutation|November 3, 2000
PMM2 mutation spectrum, including 10 novel mutations, in a large CDG type 1A family material with a focus on Scandinavian familiesC Bjursell, A Erlandson, M Nordling, et al.
Journal of Medical Genetics|November 3, 2004
Increased recurrence risk in congenital disorders of glycosylation type Ia (CDG-Ia) due to a transmission ratio distortionE Schollen, S Kjaergaard, T Martinsson, et al.
Journal of Medical Genetics|May 5, 1999
Congenital variant Rett syndrome in a girl with terminal deletion of chromosome 3pJ Wahlström, A Uller, T Johannesson, et al.
Gastroenterology|October 26, 2001
Periampullary adenomas and adenocarcinomas in familial adenomatous polyposis: cumulative risks and APC gene mutationsJ Björk, H Akerbrant, L Iselius, et al.
Nature|May 23, 1985
Amplification and enhanced expression of the c-myc oncogene in mouse SEWA tumour cellsM Schwab, G Ramsay, K Alitalo, et al.
European Journal of Human Genetics : EJHG|May 11, 1999
Cytogenetic analysis of 477 psoriatics revealed an increased frequency of aberrations involving chromosome region 11qC Enerbäck, D Holmqvist, A Inerot, et al.
Human Genetics|January 27, 2000
A genome-wide search for genes predisposing to familial psoriasis by using a stratification approachL Samuelsson, F Enlund, A Torinsson, et al.
Journal of the American Academy of Child and Adolescent Psychiatry|May 1, 1991
Autism associated with marker chromosomeC Gillberg, S Steffenburg, J Wahlström, et al.
Pageof 15

Showing results (111-120 of 146) with videos related to

Sort By:
Pageof 15
Hereditas|January 1, 1987
Isolation of selectively amplified DNA sequences from multidrug-resistant SEWA cellsF Stähl, P Sandberg, T Martinsson, et al.
Archives of Dermatological Research|February 24, 2001
Stronger association with HLA-Cw6 than with corneodesmosin (S-gene) polymorphisms in Swedish psoriasis patientsC Enerbäck, S Nilsson, F Enlund, et al.
Human Mutation|November 3, 2000
PMM2 mutation spectrum, including 10 novel mutations, in a large CDG type 1A family material with a focus on Scandinavian familiesC Bjursell, A Erlandson, M Nordling, et al.
Journal of Medical Genetics|November 3, 2004
Increased recurrence risk in congenital disorders of glycosylation type Ia (CDG-Ia) due to a transmission ratio distortionE Schollen, S Kjaergaard, T Martinsson, et al.
Journal of Medical Genetics|May 5, 1999
Congenital variant Rett syndrome in a girl with terminal deletion of chromosome 3pJ Wahlström, A Uller, T Johannesson, et al.
Gastroenterology|October 26, 2001
Periampullary adenomas and adenocarcinomas in familial adenomatous polyposis: cumulative risks and APC gene mutationsJ Björk, H Akerbrant, L Iselius, et al.
Nature|May 23, 1985
Amplification and enhanced expression of the c-myc oncogene in mouse SEWA tumour cellsM Schwab, G Ramsay, K Alitalo, et al.
European Journal of Human Genetics : EJHG|May 11, 1999
Cytogenetic analysis of 477 psoriatics revealed an increased frequency of aberrations involving chromosome region 11qC Enerbäck, D Holmqvist, A Inerot, et al.
Human Genetics|January 27, 2000
A genome-wide search for genes predisposing to familial psoriasis by using a stratification approachL Samuelsson, F Enlund, A Torinsson, et al.
Journal of the American Academy of Child and Adolescent Psychiatry|May 1, 1991
Autism associated with marker chromosomeC Gillberg, S Steffenburg, J Wahlström, et al.
Pageof 15