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Annales De Genetique|December 8, 2004
Non-lethal Hallermann-Streiff syndrome with bone fracture: report of a caseVildan Ertekin, Mukadder Ayşe Selimoğlu, Erol SelimoğluAnnales De Genetique|January 1, 1997
Familial aggregation of malignant melanoma/dysplastic naevi and tumours of the nervous system: an original syndrome of tumour pronenessM Bahuau, D Vidaud, M Kujas, et al.Annales De Genetique|January 1, 1997
Chromosome aberrations after radiotherapy in patients treated for non Hodgkin's lymphomaM A Mahé, M J André, E Moyon, et al.Annales De Genetique|January 1, 1997
Combined use of cytogenetic analysis and FISH for the identification of two antenatal de novo markers as Robertsonian translocations involving the p armsM Pierluigi, P Battaglia, C Perfumo, et al.Annales De Genetique|January 1, 1997
Multiple (up to seven) different accessory small marker chromosomes: prenatal diagnosis and follow-upR Ulmer, R A Pfeiffer, E Wiest, et al.Annales De Genetique|January 1, 1997
Characterization of two extreme variants involving the short arm of chromosome 22: are they identical?R A Conte, S M Kleyman, C Laundon, et al.Annales De Genetique|January 1, 1997
Assignment of ferritin L gene (FTL) to human chromosome band 19q13.3 by in situ hybridizationP Gasparini, S Calvano, E Memeo, et al.Annales De Genetique|January 1, 1997
Clinical applications of primed in situ labelling (PRINS) rapid identification of a marker chromosome in a fetusG V Velagaleti, N J Carpenter, A T TharapelAnnales De Genetique|January 1, 1997
18p monosomy with midline defects and a de novo satellite identified by FISHL Taine, C Goizet, Z Q Wen, et al.Pageof 129