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Cytogenetics and Cell Genetics
|
November 27, 1999
Refined physical mapping and genomic structure of the EXTL1 gene
W Wuyts, N Spieker, N Van Roy, et al.
Genes, Chromosomes & Cancer
|
September 11, 2001
Combined M-FISH and CGH analysis allows comprehensive description of genetic alterations in neuroblastoma cell lines
N Van Roy, H Van Limbergen, J Vandesompele, 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.
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.
Human Genetics
|
June 1, 1992
Reciprocal translocation between the proximal regions of the long arms of chromosomes 13 and 15 resulting in unbalanced offspring: characterization by fluorescence in situ hybridization and DNA analysis
K Mangelschots, B Van Roy, F Speleman, et al.
Human Genetics
|
December 18, 1998
Noonan-like phenotype in monozygotic twins with a duplication-deficiency of the long arm of chromosome 18 resulting from a maternal paracentric inversion
W Courtens, D Grossman, N Van Roy, et al.
European Journal of Human Genetics : EJHG
|
February 5, 1998
Identification and characterization of a novel member of the EXT gene family, EXTL2
W Wuyts, W Van Hul, J Hendrickx, et al.
European Journal of Cancer (Oxford, England : 1990)
|
January 1, 1995
1p36: every subband a suppressor?
R Versteeg, H Caron, N C Cheng, et al.
Progress in Clinical and Biological Research
|
January 1, 1994
Chromosome 1p allelic loss in neuroblastoma: prognosis, genomic imprinting and 1;17 translocations
H Caron, P van Sluis, N van Roy, et al.
American Journal of Medical Genetics
|
July 1, 1994
Proximal deletion of chromosome 21 confirmed by in situ hybridization and molecular studies
W Courtens, M B Petersen, J C Noël, et al.
Page
of 9
Search research articles
Search
Showing results (61-70 of 90) with videos related to
Sort By:
Page
of 9
Cytogenetics and Cell Genetics
|
November 27, 1999
Refined physical mapping and genomic structure of the EXTL1 gene
W Wuyts, N Spieker, N Van Roy, et al.
Genes, Chromosomes & Cancer
|
September 11, 2001
Combined M-FISH and CGH analysis allows comprehensive description of genetic alterations in neuroblastoma cell lines
N Van Roy, H Van Limbergen, J Vandesompele, 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.
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.
Human Genetics
|
June 1, 1992
Reciprocal translocation between the proximal regions of the long arms of chromosomes 13 and 15 resulting in unbalanced offspring: characterization by fluorescence in situ hybridization and DNA analysis
K Mangelschots, B Van Roy, F Speleman, et al.
Human Genetics
|
December 18, 1998
Noonan-like phenotype in monozygotic twins with a duplication-deficiency of the long arm of chromosome 18 resulting from a maternal paracentric inversion
W Courtens, D Grossman, N Van Roy, et al.
European Journal of Human Genetics : EJHG
|
February 5, 1998
Identification and characterization of a novel member of the EXT gene family, EXTL2
W Wuyts, W Van Hul, J Hendrickx, et al.
European Journal of Cancer (Oxford, England : 1990)
|
January 1, 1995
1p36: every subband a suppressor?
R Versteeg, H Caron, N C Cheng, et al.
Progress in Clinical and Biological Research
|
January 1, 1994
Chromosome 1p allelic loss in neuroblastoma: prognosis, genomic imprinting and 1;17 translocations
H Caron, P van Sluis, N van Roy, et al.
American Journal of Medical Genetics
|
July 1, 1994
Proximal deletion of chromosome 21 confirmed by in situ hybridization and molecular studies
W Courtens, M B Petersen, J C Noël, et al.
Page
of 9