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Genomics
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November 20, 1995
The gene for human gap junction protein connexin37 (GJA4) maps to chromosome 1p35.1, in the vicinity of D1S195
G Van Camp, P Coucke, F Speleman, et al.
Cancer Genetics and Cytogenetics
|
September 1, 1997
Comparative genomic hybridization analysis of human neuroblastomas: detection of distal 1p deletions and further molecular genetic characterization of neuroblastoma cell lines
N Van Roy, A Jauch, M Van Gele, et al.
Human Mutation
|
June 22, 2000
Exhaustive mutation analysis of the NF1 gene allows identification of 95% of mutations and reveals a high frequency of unusual splicing defects
L M Messiaen, T Callens, G Mortier, et al.
Cancer Genetics and Cytogenetics
|
November 1, 2006
Screening for EVI1: ectopic expression absent in T-cell acute lymphoblastic leukemia patients and cell lines
A De Weer, B Poppe, B Cauwelier, et al.
Medical and Pediatric Oncology
|
December 7, 2000
Chromosome 2 short arm translocations revealed by M-FISH analysis of neuroblastoma cell lines
N Van Roy, H Van Limbergen, J Vandesompele, et al.
Clinical Genetics
|
April 1, 1992
Detection of subtle reciprocal translocations by fluorescence in situ hybridization
F Speleman, N Van Roy, J Wiegant, et al.
Genes, Chromosomes & Cancer
|
July 1, 1991
Is t(6;20)(p21;q13) a characteristic chromosome change in endometrial polyps?
F Speleman, P Dal Cin, N Van Roy, et al.
American Journal of Medical Genetics
|
August 22, 2000
Subtelomeric familial translocation t(2;7)(q37;q35) leading to partial trisomy 7q35-->qter: molecular cytogenetic analysis and clinical phenotype in two generations
F Speleman, B Callens, K Logghe, et al.
Human Genetics
|
April 1, 1992
Molecular cytogenetic analysis of XX males using Y-specific DNA sequences, including SRY
B Van der Auwera, N Van Roy, A De Paepe, et al.
Clinical Chemistry
|
September 23, 1997
Absence of serum alanine aminotransferase activity in a neonate
J Delanghe, H Vlaminck, D Bernard, et al.
Page
of 9
Search research articles
Search
Showing results (41-50 of 90) with videos related to
Sort By:
Page
of 9
Genomics
|
November 20, 1995
The gene for human gap junction protein connexin37 (GJA4) maps to chromosome 1p35.1, in the vicinity of D1S195
G Van Camp, P Coucke, F Speleman, et al.
Cancer Genetics and Cytogenetics
|
September 1, 1997
Comparative genomic hybridization analysis of human neuroblastomas: detection of distal 1p deletions and further molecular genetic characterization of neuroblastoma cell lines
N Van Roy, A Jauch, M Van Gele, et al.
Human Mutation
|
June 22, 2000
Exhaustive mutation analysis of the NF1 gene allows identification of 95% of mutations and reveals a high frequency of unusual splicing defects
L M Messiaen, T Callens, G Mortier, et al.
Cancer Genetics and Cytogenetics
|
November 1, 2006
Screening for EVI1: ectopic expression absent in T-cell acute lymphoblastic leukemia patients and cell lines
A De Weer, B Poppe, B Cauwelier, et al.
Medical and Pediatric Oncology
|
December 7, 2000
Chromosome 2 short arm translocations revealed by M-FISH analysis of neuroblastoma cell lines
N Van Roy, H Van Limbergen, J Vandesompele, et al.
Clinical Genetics
|
April 1, 1992
Detection of subtle reciprocal translocations by fluorescence in situ hybridization
F Speleman, N Van Roy, J Wiegant, et al.
Genes, Chromosomes & Cancer
|
July 1, 1991
Is t(6;20)(p21;q13) a characteristic chromosome change in endometrial polyps?
F Speleman, P Dal Cin, N Van Roy, et al.
American Journal of Medical Genetics
|
August 22, 2000
Subtelomeric familial translocation t(2;7)(q37;q35) leading to partial trisomy 7q35-->qter: molecular cytogenetic analysis and clinical phenotype in two generations
F Speleman, B Callens, K Logghe, et al.
Human Genetics
|
April 1, 1992
Molecular cytogenetic analysis of XX males using Y-specific DNA sequences, including SRY
B Van der Auwera, N Van Roy, A De Paepe, et al.
Clinical Chemistry
|
September 23, 1997
Absence of serum alanine aminotransferase activity in a neonate
J Delanghe, H Vlaminck, D Bernard, et al.
Page
of 9