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Human Genetics|July 18, 1979
Evidence for a correlation between late replication and autosomal gene inactivation in a familial translocation t(X;21)J Couturier, B Dutrillaux, P Garber, et al.American Journal of Medical Genetics|March 1, 1992
Segregation of three reciprocal translocations in the same family: t(3;4), t(5;10), and t(15;21)L Telvi, M Folhen, O Raoul, et al.Human Genetics|January 1, 1984
Assignment of human phosphoribosylglycinamide synthetase locus to region 21q221B Chadefaux, D Allard, M O Rethoré, et al.Acta Endocrinologica|December 1, 1986
Gonadotropin responses to low dose pulsatile administration of GnRH in a case of anosmia with hypogonadotropic hypogonadism associated with gonadal dysgenesis 47 XXYJ Hazard, I Rozenberg, L Perlemuter, et al.Human Molecular Genetics|September 1, 1995
Proximal deletions of the long arm of the Y chromosome suggest a critical region associated with a specific subset of characteristic Turner stigmataS Barbaux, E Vilain, O Raoul, et al.Annales De Biologie Clinique|April 19, 2003
[Spectral karyotyping (SKY) principle, avantages and limitations]M A Belaud-Rotureau, H Elghezal, C Bernardin, et al.European Journal of Medical Genetics|June 10, 2006
Molecular cytogenetic analysis of five 2q37 deletions: refining the brachydactyly candidate regionM Chaabouni, M Le Merrer, O Raoul, et al.American Journal of Medical Genetics|November 29, 2002
Molecular characterization of partial trisomy 16q24.1-qter: clinical report and review of the literatureS Brisset, G Joly, C Ozilou, et al.American Journal of Human Genetics|March 1, 1994
Understanding the mechanism(s) of mosaic trisomy 21 by using DNA polymorphism analysisC Pangalos, D Avramopoulos, J L Blouin, et al.Journal of Medical Genetics|January 8, 2009
19q13.11 deletion syndrome: a novel clinically recognisable genetic condition identified by array comparative genomic hybridisationV Malan, O Raoul, H V Firth, et al.Pageof 3