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Genomics|July 1, 1988
Homozygous deletion of a DNA marker from chromosome 11p13 in sporadic Wilms tumorW H Lewis, H Yeger, L Bonetta, et al.Genes, Chromosomes & Cancer|May 1, 1993
Pericentric intrachromosomal insertion responsible for recurrence of del(11)(p13p14) in a familyI Henry, J Hoovers, F Barichard, et al.Nature Genetics|June 1, 1995
Primary adhalinopathy: a common cause of autosomal recessive muscular dystrophy of variable severityF Piccolo, S L Roberds, M Jeanpierre, et al.Human Genetics|August 1, 1986
The isolation of genomic recombinants for the human apolipoprotein B gene and the mapping of three common DNA polymorphisms of the gene--a useful marker for human chromosome 2N Barni, P J Talmud, P Carlsson, et al.Cytogenetics and Cell Genetics|January 1, 1989
Molecular definition of de novo and genetically transmitted WAGR-associated rearrangements of 11p13C Lavedan, F Barichard, M Azoulay, et al.Genes, Chromosomes & Cancer|December 1, 1996
Correlations of allelic imbalance of chromosome 14 with adverse prognostic parameters in 148 renal cell carcinomasC Béroud, J C Fournet, C Jeanpierre, et al.Rheumatology (Oxford, England)|December 15, 2006
Association between an endoglin gene polymorphism and systemic sclerosis-related pulmonary arterial hypertensionJ Wipff, A Kahan, E Hachulla, et al.Human Genetics|January 1, 1985
Isolation and characterisation of a cDNA clone for human apolipoprotein CI and assignment of the gene to chromosome 19F Tata, I Henry, A F Markham, et al.American Journal of Human Genetics|May 1, 1993
Myotonic dystrophy: size- and sex-dependent dynamics of CTG meiotic instability, and somatic mosaicismC Lavedan, H Hofmann-Radvanyi, P Shelbourne, et al.Proceedings of the National Academy of Sciences of the United States of America|May 1, 1989
Tumor-specific loss of 11p15.5 alleles in del11p13 Wilms tumor and in familial adrenocortical carcinomaI Henry, S Grandjouan, P Couillin, et al.Pageof 24