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Proceedings of the National Academy of Sciences of the United States of America|December 1, 1989
Contiguous gene syndromes due to deletions in the distal short arm of the human X chromosomeA Ballabio, B Bardoni, R Carrozzo, et al.Nature|December 15, 1994
Mutations in the DAX-1 gene give rise to both X-linked adrenal hypoplasia congenita and hypogonadotropic hypogonadismF Muscatelli, T M Strom, A P Walker, et al.Neurobiology of Disease|March 29, 2021
Fragile X mental retardation protein (FMRP) and metabotropic glutamate receptor subtype 5 (mGlu5) control stress granule formation in astrocytesB Di Marco, P Dell'Albani, S D'Antoni, et al.Nature|December 15, 1994
An unusual member of the nuclear hormone receptor superfamily responsible for X-linked adrenal hypoplasia congenitaE Zanaria, F Muscatelli, B Bardoni, et al.Human Molecular Genetics|November 18, 1998
Novel isoforms of the fragile X related protein FXR1P are expressed during myogenesisE W Khandjian, B Bardoni, F Corbin, et al.International Journal of Developmental Neuroscience : the Official Journal of the International Society for Developmental Neuroscience|February 15, 2015
Fragile X mental retardation protein (FMRP) interacting proteins exhibit different expression patterns during developmentC M Bonaccorso, M Spatuzza, B Di Marco, et al.Human Genetics|December 1, 1989
Close linkage of probe p212 (DXS178) to X-linked agammaglobulinemiaS Guioli, B Arveiler, B Bardoni, et al.Nature|October 10, 1991
A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding moleculesB Franco, S Guioli, A Pragliola, et al.Pageof 4