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Human Genetics|January 1, 1985
Isolation of probes detecting restriction fragment length polymorphisms from X chromosome-specific libraries: potential use for diagnosis of Duchenne muscular dystrophyM H Hofker, M C Wapenaar, N Goor, et al.
Nucleic Acids Research|April 25, 1983
Linkage analysis of two cloned DNA sequences flanking the Duchenne muscular dystrophy locus on the short arm of the human X chromosomeK E Davies, P L Pearson, P S Harper, et al.
Cancer Research|February 1, 1991
Frequent somatic imbalance of marker alleles for chromosome 1 in human primary breast carcinomaP Devilee, M van Vliet, A Bardoel, et al.
Domestic Animal Endocrinology|August 30, 2000
Porcine erythropoietin receptor: molecular cloning and expression in embryonic and fetal liverP L Pearson, T P Smith, T S Sonstegard, et al.
Human Genetics|September 1, 1993
A complex chromosomal rearrangement detected prenatally and studied by fluorescence in situ hybridizationD A Batista, C M Tuck-Muller, J E Martinez, et al.
Oncogene|September 1, 1991
Allelotype of human breast carcinoma: a second major site for loss of heterozygosity is on chromosome 6qP Devilee, M van Vliet, P van Sloun, et al.
Brain : a Journal of Neurology|August 13, 2004
Mapping of the SCA23 locus involved in autosomal dominant cerebellar ataxia to chromosome region 20p13-12.3D S Verbeek, B P van de Warrenburg, P Wesseling, et al.
Cytogenetics and Cell Genetics|May 27, 1999
Sperm analysis in a subfertile male with a Y;16 translocation, using four-color FISHJ C Giltay, P M Kastrop, C H Tiemessen, et al.
Cytometry|January 1, 1990
Direct nonradioactive in situ hybridization of somatic cell hybrid DNA to human lymphocyte chromosomesT Kievits, P Devilee, J Wiegant, et al.
American Journal of Human Genetics|April 1, 1992
Analysis of reciprocal translocations by chromosome painting: applications and limitations of the techniqueC Rosenberg, K J Blakemore, W G Kearns, et al.
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