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Human Molecular Genetics|April 18, 2000
Transgenic mice carrying large human genomic sequences with expanded CTG repeat mimic closely the DM CTG repeat intergenerational and somatic instabilityH Seznec, A S Lia-Baldini, C Duros, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|October 29, 2000
WT1 splicing alterations in Wilms' tumorsD Baudry, M Hamelin, M O Cabanis, et al.
Genes, Chromosomes & Cancer|December 1, 1995
Characterization of regions of chromosomes 12 and 16 involved in nephroblastoma tumorigenesisE Austruy, S Candon, I Henry, et al.
Cancer Genetics and Cytogenetics|August 1, 1982
Retinoblastoma, deletion 13q14, and esterase D: application of gene dosage effect to prenatal diagnosisC Junien, S Despoisse, C Turleau, et al.
American Journal of Human Genetics|April 1, 1989
A deletion map of the WAGR region on chromosome 11M Gessler, G H Thomas, P Couillin, et al.
Annales De Genetique|June 1, 1975
[Increase of the LDH-B activity in a boy with 12p trisomy by malsegregation of a maternal translocation t(12;14) (q12;p11)]M O Rethoré, J C Kaplan, C Junien, et al.
European Journal of Human Genetics : EJHG|January 1, 1993
Testing genomic imprinting in Wilm's tumorC Moutou, A Chompret, J Hochez, et al.
Neuromuscular Disorders : NMD|March 1, 1994
Expression of dystrophin-associated proteins in dystrophin-positive muscle fibers (revertants) in Duchenne muscular dystrophyK Matsumura, F M Tomé, H Collin, et al.
Human Molecular Genetics|December 1, 1994
Abnormal methylation pattern in constitutive and facultative (X inactive chromosome) heterochromatin of ICF patientsP Miniou, M Jeanpierre, V Blanquet, et al.
Annales De Genetique|January 1, 1987
[Molecular diagnosis of Duchenne and Becker muscular dystrophies. Current data]C Junien, J Boué, C Duros, et al.
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