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The EMBO Journal|September 5, 2001
The fragile X mental retardation protein binds specifically to its mRNA via a purine quartet motifC Schaeffer, B Bardoni, J L Mandel, et al.Human Genetics|May 1, 1988
Characterization of a partial deletion of the factor VIII gene in a haemophiliac with inhibitorB Bardoni, M Sampietro, M Romano, et al.American Journal of Human Genetics|April 1, 1995
Two novel SRY missense mutations reducing DNA binding identified in XY females and their mosaic fathersM Schmitt-Ney, H Thiele, P Kaltwasser, et al.Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences|November 29, 1995
Xp duplications and sex reversalE Zanaria, B Bardoni, B Dabovic, et al.Genomics|July 1, 1988
Isolation and characterization of a family of sequences dispersed on the human X chromosomeB Bardoni, S Guioli, E Raimondi, et al.Journal of Medical Genetics|July 17, 2008
Alteration of expression of muscle specific isoforms of the fragile X related protein 1 (FXR1P) in facioscapulohumeral muscular dystrophy patientsL Davidovic, S Sacconi, E G Bechara, et al.Nature Genetics|August 1, 1992
Kallmann syndrome due to a translocation resulting in an X/Y fusion geneS Guioli, B Incerti, E Zanaria, et al.American Journal of Medical Genetics|October 23, 1997
Multiple congenital anomalies, brain hypomyelination, and ocular albinism in a female with dup(X) (pter-->q24::q21.32-->qter) and random X inactivationR Carrozzo, G Arrigo, E Rossi, et al.Molecular Endocrinology (Baltimore, Md.)|February 12, 1998
A transcriptional silencing domain in DAX-1 whose mutation causes adrenal hypoplasia congenitaE Lalli, B Bardoni, E Zazopoulos, et al.Human Genetics|February 1, 1991
Mapping the gene encoding the human erythroid transcriptional factor NFE1-GF1 to Xp11.23A Caiulo, S Nicolis, P Bianchi, et al.Pageof 4