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Hereditas
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January 1, 1987
Isolation of selectively amplified DNA sequences from multidrug-resistant SEWA cells
F 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 patients
C 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 families
C 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 distortion
E 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 3p
J Wahlström, A Uller, T Johannesson, et al.
Gastroenterology
|
October 26, 2001
Periampullary adenomas and adenocarcinomas in familial adenomatous polyposis: cumulative risks and APC gene mutations
J Björk, H Akerbrant, L Iselius, et al.
Nature
|
May 23, 1985
Amplification and enhanced expression of the c-myc oncogene in mouse SEWA tumour cells
M 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 11q
C 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 approach
L Samuelsson, F Enlund, A Torinsson, et al.
Journal of the American Academy of Child and Adolescent Psychiatry
|
May 1, 1991
Autism associated with marker chromosome
C Gillberg, S Steffenburg, J Wahlström, et al.
Page
of 15
Search research articles
Search
Showing results (111-120 of 146) with videos related to
Sort By:
Page
of 15
Hereditas
|
January 1, 1987
Isolation of selectively amplified DNA sequences from multidrug-resistant SEWA cells
F 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 patients
C 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 families
C 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 distortion
E 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 3p
J Wahlström, A Uller, T Johannesson, et al.
Gastroenterology
|
October 26, 2001
Periampullary adenomas and adenocarcinomas in familial adenomatous polyposis: cumulative risks and APC gene mutations
J Björk, H Akerbrant, L Iselius, et al.
Nature
|
May 23, 1985
Amplification and enhanced expression of the c-myc oncogene in mouse SEWA tumour cells
M 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 11q
C 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 approach
L Samuelsson, F Enlund, A Torinsson, et al.
Journal of the American Academy of Child and Adolescent Psychiatry
|
May 1, 1991
Autism associated with marker chromosome
C Gillberg, S Steffenburg, J Wahlström, et al.
Page
of 15