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Genomics|February 15, 1997
Eleven X chromosome breakpoints associated with premature ovarian failure (POF) map to a 15-Mb YAC contig spanning Xq21C Sala, G Arrigo, G Torri, et al.Oncogene|December 1, 1991
Mutations in the p53 gene in myelodysplastic syndromesP Jonveaux, P Fenaux, I Quiquandon, et al.Blood|December 1, 1995
High frequency of t(12;21) in childhood B-lineage acute lymphoblastic leukemiaS P Romana, H Poirel, M Leconiat, et al.American Journal of Ophthalmology|March 25, 1998
Gillespie syndrome phenotype with a t(X;11)(p22.32;p12) de novo translocationH Dollfus, O Joanny-Flinois, M Doco-Fenzy, et al.Blood|October 1, 1991
P53 gene mutations in acute myeloid leukemia with 17p monosomyP Fenaux, P Jonveaux, I Quiquandon, et al.Leukemia|April 1, 1992
Mutations of the p53 gene in B-cell chronic lymphocytic leukemia: a report on 39 cases with cytogenetic analysisP Fenaux, C Preudhomme, J L Laï, et al.Journal of Endocrinological Investigation|January 28, 2014
Endocrine disorders in Woodhouse-Sakati syndrome: a systematic review of the literatureM Agopiantz, P Corbonnois, A Sorlin, et al.British Journal of Haematology|February 1, 1992
Mutations of the P53 gene in acute myeloid leukaemiaP Fenaux, C Preudhomme, I Quiquandon, et al.Annales De Biologie Clinique|July 11, 2006
[A case of de novo acute basophilic leukaemia: diagnostic criteria and review of the literature]A Staal-Viliare, V Latger-Cannard, J P Rault, et al.American Journal of Human Genetics|April 29, 1998
A human homologue of the Drosophila melanogaster diaphanous gene is disrupted in a patient with premature ovarian failure: evidence for conserved function in oogenesis and implications for human sterilityS Bione, C Sala, C Manzini, et al.Pageof 10