|1.||Meeths, Marie: 1 article (07/2014)|
|2.||Bryceson, Yenan T: 1 article (07/2014)|
|3.||Henter, Jan-Inge: 1 article (07/2014)|
|4.||Müller, Martha-Lena: 1 article (07/2014)|
|5.||Löfstedt, Alexandra: 1 article (07/2014)|
|6.||Chiang, Samuel C C: 1 article (07/2014)|
|7.||Tesi, Bianca: 1 article (07/2014)|
|8.||Käser, L: 1 article (01/2007)|
|9.||Suter-Meyer, E: 1 article (01/2007)|
|10.||Vetter, W: 1 article (01/2007)|
|1.||Rett Syndrome (Rett's Disorder)
01/01/2006 - "Here, we summarize the recent findings that highlight how certain inherited diseases, such as Rett syndrome, Immunodeficiency-centromeric instability-facial anomalies syndrome, and facioscapulohumeral muscular dystrophy, result from altered gene silencing."
08/01/2003 - "These include: alpha-thalassemia/mental retardation syndrome, X-linked (ATR-X); Rett syndrome (RS); immunodeficiency-centromeric instability-facial anomalies syndrome (ICF); Rubinstein-Taybi syndrome (RSTS); and Coffin-Lowry syndrome (CLS)."
04/01/1977 - "In addition, a patient with a variable immunodeficiency syndrome that affected the bone marrow-derived (B-) cell system had recurrent infection with M. "
01/17/1986 - "Five cases (3 men, 2 women) of late-onset variable immunodeficiency syndrome (CVID), characterized by similar clinical and immunological findings as well as histological demonstration of chronic granulomatous infection, are reported. "
|3.||Coffin-Lowry Syndrome (Syndrome, Coffin-Lowry)
|4.||Facioscapulohumeral Muscular Dystrophy
|5.||Multiple Endocrine Neoplasia Type 2a (MEN 2)