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Heart Rhythm
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January 10, 2006
Long QT syndrome caused by a large duplication in the KCNH2 (HERG) gene undetectable by current polymerase chain reaction-based exon-scanning methodologies
Tamara T Koopmann, Marielle Alders, Roselie J Jongbloed, et al.
European Journal of Human Genetics : EJHG
|
January 1, 1994
Parental imprinting of human chromosome region 11p15.3-pter involved in the Beckwith-Wiedemann syndrome and various human neoplasia
M Mannens, J M Hoovers, E Redeker, et al.
The Journal of Biological Chemistry
|
September 25, 1998
The human chitotriosidase gene. Nature of inherited enzyme deficiency
R G Boot, G H Renkema, M Verhoek, et al.
Genomics
|
February 1, 1992
High-resolution localization of 69 potential human zinc finger protein genes: a number are clustered
J M Hoovers, M Mannens, R John, et al.
Human Genetics
|
April 10, 2002
A locus for hereditary capillary malformations mapped on chromosome 5q
Corstiaan C Breugem, Marielle Alders, Georgette B Salieb-Beugelaar, et al.
Progress in Biophysics and Molecular Biology
|
November 26, 2008
An intronic mutation leading to incomplete skipping of exon-2 in KCNQ1 rescues hearing in Jervell and Lange-Nielsen syndrome
Zahurul A Bhuiyan, Tarek S Momenah, Ahmad S Amin, et al.
Genomics
|
March 1, 1993
High-resolution chromosomal localization of the human calcitonin/CGRP/IAPP gene family members
J M Hoovers, E Redeker, F Speleman, et al.
Genomics
|
May 1, 1992
The generation of ordered sets of cosmid DNA clones from human chromosome region 11p
I J Heding, A C Ivens, J Wilson, et al.
Nature Genetics
|
June 1, 1993
Allelic loss of chromosome 1p36 in neuroblastoma is of preferential maternal origin and correlates with N-myc amplification
H Caron, P van Sluis, M van Hoeve, et al.
Genes, Chromosomes & Cancer
|
April 2, 1998
Cytogenetic and molecular analysis of cellular atypical mesoblastic nephroma
F Speleman, E van den Berg, C Dhooge, et al.
Page
of 18
Search research articles
Search
Showing results (51-60 of 172) with videos related to
Sort By:
Page
of 18
Heart Rhythm
|
January 10, 2006
Long QT syndrome caused by a large duplication in the KCNH2 (HERG) gene undetectable by current polymerase chain reaction-based exon-scanning methodologies
Tamara T Koopmann, Marielle Alders, Roselie J Jongbloed, et al.
European Journal of Human Genetics : EJHG
|
January 1, 1994
Parental imprinting of human chromosome region 11p15.3-pter involved in the Beckwith-Wiedemann syndrome and various human neoplasia
M Mannens, J M Hoovers, E Redeker, et al.
The Journal of Biological Chemistry
|
September 25, 1998
The human chitotriosidase gene. Nature of inherited enzyme deficiency
R G Boot, G H Renkema, M Verhoek, et al.
Genomics
|
February 1, 1992
High-resolution localization of 69 potential human zinc finger protein genes: a number are clustered
J M Hoovers, M Mannens, R John, et al.
Human Genetics
|
April 10, 2002
A locus for hereditary capillary malformations mapped on chromosome 5q
Corstiaan C Breugem, Marielle Alders, Georgette B Salieb-Beugelaar, et al.
Progress in Biophysics and Molecular Biology
|
November 26, 2008
An intronic mutation leading to incomplete skipping of exon-2 in KCNQ1 rescues hearing in Jervell and Lange-Nielsen syndrome
Zahurul A Bhuiyan, Tarek S Momenah, Ahmad S Amin, et al.
Genomics
|
March 1, 1993
High-resolution chromosomal localization of the human calcitonin/CGRP/IAPP gene family members
J M Hoovers, E Redeker, F Speleman, et al.
Genomics
|
May 1, 1992
The generation of ordered sets of cosmid DNA clones from human chromosome region 11p
I J Heding, A C Ivens, J Wilson, et al.
Nature Genetics
|
June 1, 1993
Allelic loss of chromosome 1p36 in neuroblastoma is of preferential maternal origin and correlates with N-myc amplification
H Caron, P van Sluis, M van Hoeve, et al.
Genes, Chromosomes & Cancer
|
April 2, 1998
Cytogenetic and molecular analysis of cellular atypical mesoblastic nephroma
F Speleman, E van den Berg, C Dhooge, et al.
Page
of 18