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American Journal of Medical Genetics|February 1, 1991
Fragile X syndrome in an extended family with special reference to an affected male with Klinefelter syndromeM A Voelckel, M C Pellissier, C Piquet, et al.Nucleic Acids Research|March 25, 1987
Mapping of DNA markers close to the fragile site on the human X chromosome at Xq27.3M Patterson, S Kenwrick, S Thibodeau, et al.Genomics|August 1, 1989
In situ hybridization and pulsed-field gel analysis define two major minisatellite loci: 1q23 for minisatellite 33.6 and 7q35-q36 for minisatellite 33.15G Chimini, M G Mattei, E Passage, et al.Genomics|August 1, 1989
Large-scale mapping and chromosome jumping in the q27 region of the human X chromosomeC Nguyen, A M Poustka, M Djabali, et al.Human Genetics|July 1, 1986
Assignment of human uroporphyrinogen decarboxylase (URO-D) to the p34 band of chromosome 1A Dubart, M G Mattei, N Raich, et al.Human Genetics|February 1, 1993
Physical mapping of microdeletions of the chromosome 17 short arm associated with Smith-Magenis syndromeA Moncla, L Piras, O F Arbex, et al.Pediatrie|January 1, 1992
[Molecular biology in genetic counseling of Duchenne and Becker myopathy]N Philip, M A Voelckel, L Girardot, et al.The EMBO Journal|November 1, 1987
Large scale physical mapping in the q27 region of the human X chromosome: the coagulation factor IX gene and the mcf.2 transforming sequence are separated by at most 270 kilobase pairs and are surrounded by several 'HTF islands'C Nguyen, P Pontarotti, D Birnbaum, et al.European Journal of Human Genetics : EJHG|January 1, 1996
Unexpected inheritance of the (CGG)n trinucleotide expansion in a fragile X syndrome familyP Malzac, V Biancalana, M A Voelckel, et al.Human Genetics|March 1, 1992
Physical mapping of an Xq-proximal interstitial duplication in a maleF Muscatelli, J M Verna, N Philip, et al.Pageof 14