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Clinical Genetics|February 1, 1990
Trisomy 17p due to a t(8;17) (p23;p11.2)pat translocation. Case report and review of the literatureC Schrander-Stumpel, J Schrander, J P Fryns, et al.Journal De Genetique Humaine|September 1, 1989
A "new" epi-metaphyseal skeletal dysplasia in four members of a familyJ P Fryns, F De Bisschop, H Van den BergheHuman Genetics|January 19, 1979
Partial monosomy of the long arm of chromosome 16: a distinct clinical entity?J P Fryns, J Bande-Knops, H Van Den BergheGenetic Counseling (Geneva, Switzerland)|January 1, 1993
The Larsen syndrome. The diagnostic contribution of the analysis of the metacarpophalangeal pattern profileL De Smet, E Legius, G Fabry, et al.Human Genetics|January 1, 1983
Langer-Giedion syndrome and deletion of the long arm of chromosome 8. Confirmation of the critical segment to 8q23J P Fryns, G Heremans, J Marien, et al.Cytogenetic and Genome Research|September 7, 2006
Molecular cytogenetic characterization of a constitutional complex intrachromosomal 4q rearrangement in a patient with multiple congenital anomaliesB Thienpont, M Gewillig, J-P Fryns, et al.Clinical Genetics|November 1, 1988
Fertility and X-chromosome rearrangements: isodicentric X-chromosome formation in the mother and Xp deletion in her daughterJ P Fryns, A Kleczkowska, P Debucquoy, et al.Journal of Medical Genetics|April 1, 1992
Interstitial deletion of the distal long arm of chromosome 4P Sarda, G Lefort, J P Fryns, et al.Annales De Genetique|January 1, 1986
Double autosomal chromosomal aberration (3p trisomy/9p monosomy) and sex-reversalJ P Fryns, A Kleczkowska, P Casaer, et al.Pageof 89