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Journal De Genetique Humaine|March 1, 1976
[Translocation 46,XY,t(2;5) (q37;q14) and mental retardation. Clinical and cytogenetic study]S Gilgenkrantz, R Walbaum, G Mauuary, et al.Humangenetik|January 1, 1975
[Late replication and X-autosome traslocation a case with banding patterns autoradiographic and B.U.D.R. studies (author's transl)]S Gilgenkrantz, G Mauuary, B Dutrillaux, et al.Archives Francaises De Pediatrie|February 1, 1985
[Partial trisomy of chromosome 3 resulting from paternal translocation]M Cointin, D Olive, S Gilgenkrantz, et al.Human 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.Human Genetics|June 1, 1989
Molecular characterization of a ring chromosome 14 showing that the PI locus is centromeric to the D14S1 and IGH lociG Keyeux, S Gilgenkrantz, G Lefranc, et al.Human Genetics|October 1, 1990
Distal trisomy 14q. II. Molecular study of the 14q32 locus in two cases of chromosome 14 rearrangements with partial duplicationG Keyeux, S Gilgenkrantz, G Lefranc, et al.Journal De Genetique Humaine|July 1, 1984
[Mental retardation and fragile X chromosome. Clinical and cytogenetic study of 3 families]S Gilgenkrantz, J Boué, M J Grégoire, et al.Human Molecular Genetics|July 1, 1996
Cloning and characterization of DXS6673E, a candidate gene for X-linked mental retardation in Xq13.1S M van der Maarel, I H Scholten, I Huber, et al.Journal of Medical Genetics|September 1, 1989
3M dwarfism: a study of two further sibsM Feldmann, S Gilgenkrantz, S Parisot, et al.Human Genetics|February 1, 1986
A case of female hemophilia with a 46,XXr karyotype studied with X-chromosome DNA probesS Gilgenkrantz, M E Briquel, J L Mandel, et al.Pageof 24