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Annales De Genetique|May 26, 1998
Application of fluorescence in situ hybridization to the identification of different marker chromosomesM R Verschraegen-Spae, B Quack, S Rousseaux, et al.Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|October 6, 1998
[Unusual presentation of nephroblastomatosis]J Santiago, R Bouvier, J M Pouillaude, et al.Human Reproduction (Oxford, England)|August 19, 2006
Rare Robertsonian translocations and meiotic behaviour: sperm FISH analysis of t(13;15) and t(14;15) translocations: a case reportK Moradkhani, J Puechberty, S Bhatt, et al.Annales De Genetique|September 1, 2004
Balanced complex chromosomal rearrangements (BCCR) with at least three chromosomes and three or more breakpoints: report of three new casesJ Lespinasse, M O Réthoré, M O North, et al.Molecular Human Reproduction|October 5, 2007
Breakpoint characterization: a new approach for segregation analysis of paracentric inversion in human spermS Bhatt, K Moradkhani, K Mrasek, et al.The Journal of Clinical Endocrinology and Metabolism|November 5, 1997
A large multiple endocrine neoplasia type 1 family with clinical expression suggestive of anticipationS Giraud, H Choplin, B T Teh, et al.European Journal of Human Genetics : EJHG|September 12, 2000
High resolution comparative genomic hybridisation analysis reveals imbalances in dyschromosomal patients with normal or apparently balanced conventional karyotypesM Kirchhoff, H Rose, J Maahr, et al.Annales De Genetique|December 8, 2004
A submicroscopic unbalanced subtelomeric translocation t(2p;10q) identified by fluorescence in situ hybridization: fetus with increased nuchal translucency and normal standard karyotype with later growth and developmental delay, rhombencephalosynapsis (RES)J Lespinasse, H Testard, F Nugues, et al.Journal of Medical Genetics|October 21, 1999
Two unrelated patients with inversions of the X chromosome and non-specific mental retardation: physical and transcriptional mapping of their common breakpoint region in Xq13.1L Villard, S Briault, A M Lossi, et al.Molecular Human Reproduction|January 3, 2001
Identification of human candidate genes for male infertility by digital differential displayC Olesen, C Hansen, E Bendsen, et al.Pageof 3