PCH’s Keeping Kids in No Distress (KKIND) service aims to help children cope with medical trauma, anxiety and distress caused by illness, injury or hospitalisation. The KKIND team …

Pontocerebellar hypoplasia (PCH) is a heterogeneous group of rare neurodegenerative disorders caused by genetic mutations and characterised by progressive atrophy of various parts of the …

Different plotting symbols are available in R. The graphical argument used to specify point shapes is pch. The different points symbols commonly used in R are shown in the figure below : The …

Kiind supports families raising children living with disability, developmental delay, autism, genetic, rare, undiagnosed and/or chronic conditions. Their experienced team all have lived experience …

2009年9月8日 · The phenotypic spectrum of TSEN54 pontocerebellar hypoplasia (TSEN54-PCH) includes three PCH phenotypes (thought to be distinct entities before the molecular basis of …

2012年3月16日 · Pontocerebellar hypoplasias (PCH) are a group of rare heterogeneous conditions characterized by prenatal development of an abnormally small cerebellum and …

Paroxysmal cold hemoglobinuria (PCH) or Donath–Landsteiner hemolytic anemia (DLHA) is an autoimmune hemolytic anemia featured by complement-mediated intravascular hemolysis …

2016年5月5日 · pch参数用于指定绘图符号的类型，包括不同的点、线和符号形状。通过选择合适的pch值，我们可以在可视化图中显示数据点的标签。除了实心圆点（pch = 16）之外，pch参 …

Pontocerebellar hypoplasia type 2 (PCH2) is a rare, relatively unknown disease that causes severe physical and mental disabilities from birth and a reduced life expectancy in affected …

2014年5月5日 · Pontocerebellar hypoplasias (PCH) are a group of very rare heterogeneous conditions characterized by prenatal development of an abnormally small cerebellum and …