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  • Rubinstein-Taybi syndrome: Treatments and life expectancy
    Rubinstein-Taybi syndrome (RSTS) is a rare genetic condition that can lead to distinctive facial features, broad thumbs, and moderate to severe intellectual disability
  • Rubinstein-taybi syndrome | About the Disease | GARD - Genetic and Rare . . .
    Rubinstein-Taybi syndrome (RTS) is a syndrome characterized by broad thumbs and toes, short stature, distinctive facial features, and varying degrees of intellectual disability
  • RSTS E - Wikipedia
    RSTS ( ˈrɪstɪs ) is a multi-user time-sharing operating system developed by Digital Equipment Corporation (DEC, now part of Hewlett-Packard) for the PDP-11 series of 16-bit minicomputers
  • Rubinstein-Taybi Syndrome - Symptoms, Causes, Treatment - NORD
    Rubinstein-Taybi syndrome (RSTS) is a rare genetic disorder that affects many organ systems RSTS is characterized by growth delays, distinctive facial features, intellectual disability (with an average IQ of 25-79), broad and often angulated thumbs and great toes (halluces) and feeding difficulties (dysphagia)
  • Rubinstein-Taybi syndrome - MedlinePlus
    Rubinstein-Taybi syndrome is a condition characterized by short stature, moderate to severe intellectual disability, distinctive facial features, and broad thumbs and first toes Additional features of the disorder can include eye abnormalities, heart and kidney defects, dental problems, and obesity
  • Rubinstein-Taybi syndrome: clinical features, genetic basis, diagnosis . . .
    Rubinstein-Taybi syndrome (RSTS) is an extremely rare autosomal dominant genetic disease, with an estimated prevalence of one case per 125,000 live births RSTS is characterized by typical facial features, microcephaly, broad thumbs and first toes,
  • Rubinstein-Taybi Syndrome: A Complete Overview - DermNet
    What is Rubinstein-Taybi syndrome? Rubinstein-Taybi syndrome (RTS) or broad thumb-hallux syndrome is a rare genetic condition usually caused by mutations of the CREBBP or EP300 genes
  • Entry - #180849 - RUBINSTEIN-TAYBI SYNDROME 1; RSTS1 - OMIM
    Rubinstein-Taybi syndrome is a multiple congenital anomaly syndrome characterized by mental retardation, postnatal growth deficiency, microcephaly, broad thumbs and halluces, and dysmorphic facial features
  • Rubinstein-Taybi Syndrome - PubMed
    Clinical characteristics: Rubinstein-Taybi syndrome (RSTS) is characterized by distinctive facial features, broad and often angulated thumbs and halluces, short stature, and moderate-to-severe intellectual disability
  • Rubinstein-Taybi Syndrome: A Model of Epigenetic Disorder
    The Rubinstein-Taybi syndrome (RSTS) is a rare congenital developmental disorder characterized by a typical facial dysmorphism, distal limb abnormalities, intellectual disability, and many additional phenotypical features It occurs at between 1 100,000 and 1 125,000 births





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