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M Hansson

Showing results (271-280 of 300) with videos related to

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NPJ Precision Oncology|September 6, 2018
A platform for phenotypic discovery of therapeutic antibodies and targets applied on Chronic Lymphocytic LeukemiaA Ljungars, L Mårtensson, J Mattsson, et al.
Human Genetics|August 4, 2005
High-resolution array-CGH profiling of germline and tumor-specific copy number alterations on chromosome 22 in patients affected with schwannomasTeresita Díaz de Ståhl, Caisa M Hansson, Cecilia de Bustos, et al.
BMJ (Clinical Research Ed.)|June 30, 2005
Selective chromosome analysis in couples with two or more miscarriages: case-control studyMaureen T M Franssen, Johanna C Korevaar, Nico J Leschot, et al.
Nederlands Tijdschrift Voor Geneeskunde|May 3, 2007
[Risk factors for structural chromosomal abnormality in > or = 2 miscarriages, as an instrument for selective karyotyping]M T M Franssen, J C Korevaar, N J Leschot, et al.
Leukemia|February 6, 2014
Expert panel consensus statement on the optimal use of pomalidomide in relapsed and refractory multiple myelomaM A Dimopoulos, X Leleu, A Palumbo, et al.
Nature Communications|September 5, 2020
Publisher Correction: Single-cell analysis uncovers fibroblast heterogeneity and criteria for fibroblast and mural cell identification and discriminationLars Muhl, Guillem Genové, Stefanos Leptidis, et al.
Nature Communications|August 10, 2020
Single-cell analysis uncovers fibroblast heterogeneity and criteria for fibroblast and mural cell identification and discriminationLars Muhl, Guillem Genové, Stefanos Leptidis, et al.
Clinical Genetics|May 22, 2010
X-chromosome duplications in males with mental retardation: pathogenic or benign variants?A C J Gijsbers, N S den Hollander, A T J M Helderman-van de Enden, et al.
European Journal of Human Genetics : EJHG|November 11, 2010
The clinical spectrum of complete FBN1 allele deletionsYvonne Hilhorst-Hofstee, Ben C J Hamel, Joke B G M Verheij, et al.
Arthritis & Rheumatology (Hoboken, N.J.)|February 28, 2014
Features of the synovium of individuals at risk of developing rheumatoid arthritis: implications for understanding preclinical rheumatoid arthritisM J H de Hair, M G H van de Sande, T H Ramwadhdoebe, et al.
Pageof 30

Showing results (271-280 of 300) with videos related to

Sort By:
Pageof 30
NPJ Precision Oncology|September 6, 2018
A platform for phenotypic discovery of therapeutic antibodies and targets applied on Chronic Lymphocytic LeukemiaA Ljungars, L Mårtensson, J Mattsson, et al.
Human Genetics|August 4, 2005
High-resolution array-CGH profiling of germline and tumor-specific copy number alterations on chromosome 22 in patients affected with schwannomasTeresita Díaz de Ståhl, Caisa M Hansson, Cecilia de Bustos, et al.
BMJ (Clinical Research Ed.)|June 30, 2005
Selective chromosome analysis in couples with two or more miscarriages: case-control studyMaureen T M Franssen, Johanna C Korevaar, Nico J Leschot, et al.
Nederlands Tijdschrift Voor Geneeskunde|May 3, 2007
[Risk factors for structural chromosomal abnormality in > or = 2 miscarriages, as an instrument for selective karyotyping]M T M Franssen, J C Korevaar, N J Leschot, et al.
Leukemia|February 6, 2014
Expert panel consensus statement on the optimal use of pomalidomide in relapsed and refractory multiple myelomaM A Dimopoulos, X Leleu, A Palumbo, et al.
Nature Communications|September 5, 2020
Publisher Correction: Single-cell analysis uncovers fibroblast heterogeneity and criteria for fibroblast and mural cell identification and discriminationLars Muhl, Guillem Genové, Stefanos Leptidis, et al.
Nature Communications|August 10, 2020
Single-cell analysis uncovers fibroblast heterogeneity and criteria for fibroblast and mural cell identification and discriminationLars Muhl, Guillem Genové, Stefanos Leptidis, et al.
Clinical Genetics|May 22, 2010
X-chromosome duplications in males with mental retardation: pathogenic or benign variants?A C J Gijsbers, N S den Hollander, A T J M Helderman-van de Enden, et al.
European Journal of Human Genetics : EJHG|November 11, 2010
The clinical spectrum of complete FBN1 allele deletionsYvonne Hilhorst-Hofstee, Ben C J Hamel, Joke B G M Verheij, et al.
Arthritis & Rheumatology (Hoboken, N.J.)|February 28, 2014
Features of the synovium of individuals at risk of developing rheumatoid arthritis: implications for understanding preclinical rheumatoid arthritisM J H de Hair, M G H van de Sande, T H Ramwadhdoebe, et al.
Pageof 30