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Duodecim; Laaketieteellinen Aikakauskirja
|
August 20, 2002
[Preimplantation diagnostics]
J Lähdetie, N Horelli-Kuitunen
Genomics
|
January 16, 1999
Characterization of a novel gene, PNUTL2, on human chromosome 17q22-q23 and its exclusion as the Meckel syndrome gene
P Paavola, N Horelli-Kuitunen, A Palotie, et al.
Annals of Medicine
|
April 1, 1996
High-resolution fluorescence in situ hybridization: a new approach in genome mapping
A Palotie, M Heiskanen, M Laan, et al.
American Journal of Medical Genetics
|
October 6, 1999
Interstitial deletion of bands 11q21-->22.3 in a three-year-old girl defined using fluorescence in situ hybridization on metaphase chromosomes
N Horelli-Kuitunen, N Gahmberg, M Eeva, et al.
Cytogenetics and Cell Genetics
|
March 7, 2000
Assignment of ACVR2 and ACVR2B the human activin receptor type II and IIB genes to chromosome bands 2q22.2-->q23.3 and 3p22 and the human follistatin gene (FST) to chromosome 5q11.2 by FISH
J Bondestam, N Horelli-Kuitunen, K Hildén, et al.
Genome Research
|
August 1, 1998
Mouse palmitoyl protein thioesterase: gene structure and expression of cDNA
T Salonen, E Hellsten, N Horelli-Kuitunen, et al.
Human Molecular Genetics
|
September 15, 1998
Gene defect behind APECED: a new clue to autoimmunity
P Björses, J Aaltonen, N Horelli-Kuitunen, et al.
Genomics
|
October 27, 1997
Cloning of mouse type XV collagen sequences and mapping of the corresponding gene to 4B1-3. Comparison of mouse and human alpha 1 (XV) collagen sequences indicates divergence in the number of small collagenous domains
P M Hägg, N Horelli-Kuitunen, L Eklund, et al.
Genomics
|
May 8, 1998
Cloning of a novel human putative type Ia integral membrane protein mapping to 21q22.3
M L Yaspo, J Aaltonen, N Horelli-Kuitunen, et al.
Cytogenetics and Cell Genetics
|
March 7, 2000
Assignment of laminin alpha 2-chain gene (Lama2) to mouse chromosome 10A4-B1 by fluorescence in situ hybridization
R Sallinen, W Kuang, E Engvall, et al.
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Search research articles
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Showing results (1-10 of 35) with videos related to
Sort By:
Page
of 4
Duodecim; Laaketieteellinen Aikakauskirja
|
August 20, 2002
[Preimplantation diagnostics]
J Lähdetie, N Horelli-Kuitunen
Genomics
|
January 16, 1999
Characterization of a novel gene, PNUTL2, on human chromosome 17q22-q23 and its exclusion as the Meckel syndrome gene
P Paavola, N Horelli-Kuitunen, A Palotie, et al.
Annals of Medicine
|
April 1, 1996
High-resolution fluorescence in situ hybridization: a new approach in genome mapping
A Palotie, M Heiskanen, M Laan, et al.
American Journal of Medical Genetics
|
October 6, 1999
Interstitial deletion of bands 11q21-->22.3 in a three-year-old girl defined using fluorescence in situ hybridization on metaphase chromosomes
N Horelli-Kuitunen, N Gahmberg, M Eeva, et al.
Cytogenetics and Cell Genetics
|
March 7, 2000
Assignment of ACVR2 and ACVR2B the human activin receptor type II and IIB genes to chromosome bands 2q22.2-->q23.3 and 3p22 and the human follistatin gene (FST) to chromosome 5q11.2 by FISH
J Bondestam, N Horelli-Kuitunen, K Hildén, et al.
Genome Research
|
August 1, 1998
Mouse palmitoyl protein thioesterase: gene structure and expression of cDNA
T Salonen, E Hellsten, N Horelli-Kuitunen, et al.
Human Molecular Genetics
|
September 15, 1998
Gene defect behind APECED: a new clue to autoimmunity
P Björses, J Aaltonen, N Horelli-Kuitunen, et al.
Genomics
|
October 27, 1997
Cloning of mouse type XV collagen sequences and mapping of the corresponding gene to 4B1-3. Comparison of mouse and human alpha 1 (XV) collagen sequences indicates divergence in the number of small collagenous domains
P M Hägg, N Horelli-Kuitunen, L Eklund, et al.
Genomics
|
May 8, 1998
Cloning of a novel human putative type Ia integral membrane protein mapping to 21q22.3
M L Yaspo, J Aaltonen, N Horelli-Kuitunen, et al.
Cytogenetics and Cell Genetics
|
March 7, 2000
Assignment of laminin alpha 2-chain gene (Lama2) to mouse chromosome 10A4-B1 by fluorescence in situ hybridization
R Sallinen, W Kuang, E Engvall, et al.
Page
of 4