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Genomics|December 10, 1995
A yeast artificial chromosome contig that spans the RB1-D13S31 interval on human chromosome 13 and encompasses the frequently deleted region in B-cell chronic lymphocytic leukemiaL Hawthorn, T Roberts, E Verlind, et al.
Journal of Child Neurology|May 11, 2000
Novel missense mutation in the L1 gene in a child with corpus callosum agenesis, retardation, adducted thumbs, spastic paraparesis, and hydrocephalusL Sztriha, P Frossard, R M Hofstra, et al.
European Journal of Human Genetics : EJHG|January 1, 1995
An integrated map of human chromosome 13 allowing regional localization of genetic markersR F Kooy, A Wijngaard, E Verlind, et al.
Human Genetics|June 1, 1993
Physical localisation of the chromosomal marker D13S31 places the Wilson disease locus at the junction of bands q14.3 and q21.1 of chromosome 13R F Kooy, A Y Van der Veen, E Verlind, et al.
Human Genetics|August 1, 1992
Identification of crossovers in Wilson disease families as reference points for a genetic localization of the geneH Scheffer, R H Houwen, G J Te Meerman, et al.
Genes, Chromosomes & Cancer|November 7, 2000
New comprehensive denaturing-gradient-gel- electrophoresis assay for KRAS mutation detection applied to paraffin-embedded tumoursV M Hayes, J L Westra, E Verlind, et al.
The Journal of Investigative Dermatology|March 25, 2000
Exempting homologous pseudogene sequences from polymerase chain reaction amplification allows genomic keratin 14 hotspot mutation analysisP H Hut, P v d Vlies, M F Jonkman, et al.
Human Genetics|September 1, 1990
Frequency of the delta F508 mutation and XV2c,KM19 haplotypes in cystic fibrosis families from The Netherlands: haplotypes without delta F508 still in disequilibriumH Scheffer, D J Bruinvels, G J te Meerman, et al.
European Journal of Human Genetics : EJHG|January 1, 1994
A deletion hybrid breakpoint map of the chromosomal region 13q14-q21 orders 19 genetic markers in 10 intervalsR F Kooy, E Verlind, R H Houwen, et al.
Brain Pathology (Zurich, Switzerland)|July 23, 1999
High frequency of TP53 mutations in juvenile pilocytic astrocytomas indicates role of TP53 in the development of these tumorsV M Hayes, C M Dirven, A Dam, et al.
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