|1.||Duchenne Muscular Dystrophy (Muscular Dystrophy, Becker)
|4.||Muscular Dystrophies (Muscular Dystrophy)
|5.||Lesch-Nyhan Syndrome (Choreoathetosis Self Mutilation Hyperuricemia Syndrome)
|1.||Henríquez-Olguín, Carlos: 2 articles (07/2015 - 01/2013)|
|2.||Valladares, Denisse: 2 articles (07/2015 - 01/2013)|
|3.||Altamirano, Francisco: 2 articles (07/2015 - 01/2013)|
|4.||Jaimovich, Enrique: 2 articles (07/2015 - 01/2013)|
|5.||Allen, Paul D: 2 articles (07/2015 - 01/2013)|
|6.||Tremblay, Jacques P: 2 articles (01/2012 - 11/2010)|
|7.||López, José R: 1 article (07/2015)|
|8.||Pelosi, Laura: 1 article (01/2015)|
|9.||Coggi, Angela: 1 article (01/2015)|
|10.||Forcina, Laura: 1 article (01/2015)|
08/01/2007 - "The dystrophinopathies comprise a group of X-linked genetic diseases that feature dystrophin deficiency. "
07/01/2015 - "Duchenne muscular dystrophy is a fatal X-linked genetic disease, caused by mutations in the dystrophin gene, which cause functional loss of this protein. "
01/01/2015 - "Duchenne muscular dystrophy (DMD) is a X-linked genetic disease in which the absence of dystrophin leads to progressive lethal skeletal muscle degeneration. "
11/01/2013 - "Duchenne muscular dystrophy (DMD) is an X-linked genetic disease, caused by the absence of the dystrophin protein. "
01/01/2013 - "Duchenne Muscular Dystrophy (DMD) is a recessive X-linked genetic disease, caused by mutations in the gene encoding dystrophin. "
|2.||Hypoxanthine Phosphoribosyltransferase (Hypoxanthine Guanine Phosphoribosyltransferase)IBA
01/01/2004 - "Lesch-Nyhan syndrome (LSN, McKusick 300322) is an X-linked genetic disease due, in its typical form, to the complete absence of hypoxanthine-guanine phosphoribosyltransferase (HPRT, EC 22.214.171.124) enzyme activity. "
11/01/2006 - "Lesch-Nyhan disease (LND), an X-linked genetic disease caused by complete deficiency of the enzyme hypoxanthine-guanine phosphoribosyltransferase (HPRT), is characterized by hyperuricemia and psychiatric disturbance, mainly self-aggressiveness. "
|3.||CD40 Ligand (CD40L)IBA
|4.||Cytokine Receptors (Cytokine Receptor)IBA
|7.||Factor IX (PTC)FDA LinkGeneric
|1.||Transplantation (Transplant Recipients)
12/01/1989 - "This suggests that the biotinylated Y probe can be applied to the determination of X-linked genetic diseases and sex abnormality, forensic analysis, sex determination of sportsmen and women, heterosexual transplantation of bone marrow, etc. It could become a convenient means for genetic diagnosis."