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American Journal of Medical Genetics|September 1, 1982
Association of del(11)(p15.1p12), aniridia, catalase deficiency, and cardiomyopathyS Gilgenkrantz, C Vigneron, M J Gregoire, et al.Journal De Genetique Humaine|March 1, 1983
[Chromosome 11 and cancer]M J Gregoire, C Pernot, F Himont, et al.Journal of Medical Genetics|December 1, 1981
Partial proximal trisomy of the long arm of chromosome 5 (q13 leads to q22) resulting from maternal insertion der ins (10;5)S Gilgenkrantz, P Dulucq, J L Bresson, et al.Bulletin De L'Association Des Anatomistes|June 1, 1976
[Cytogenetic studies in spontaneous abortions]S Gilgenkrantz, M J Gregoire, F StreiffComptes Rendus Des Seances De La Societe De Biologie Et De Ses Filiales|January 1, 1976
[Action of 5-bromodeoxyuridine as a function of time on the aspect of chromosomes. Attempt at interpretation]S Gilgenkrantz, M J Gregoire, F StreiffHuman Genetics|January 1, 1981
Proximal trisomy 13. A family with balanced reciprocal translocation t(8;13) in seven members and Robertsonian translocation t(13;14) in three membersS Gilgenkrantz, C Defeche, S Stehlin, et al.Nature|October 13, 1983
c-Ha-ras1 is not deleted in aniridia-Wilms' tumour associationC Huerre, S Despoisse, S Gilgenkrantz, et al.Human Genetics|January 1, 1984
The gene for human fibroblast interferon (IFB) maps to 9p21L Henry, J Sizun, C Turleau, et al.Journal De Genetique Humaine|July 1, 1984
[Fragile site on chromosome 2 (q11) in a case of familial lymphohistiocytosis]S Gilgenkrantz, M J Gregoire, M Chery, et al.Pediatrie|January 1, 1989
[Noonan's syndrome and its cardiovascular dysplasia. Apropos of 64 cases]C Pernot, A M Worms, F Marçon, et al.Pageof 45