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meritoriousness    
n. 极好

极好

meritoriousness
n 1: the quality of being deserving (e.g., deserving
assistance); "there were many children whose deservingness
he recognized and rewarded" [synonym: {deservingness}, {merit},
{meritoriousness}]


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英文字典中文字典相关资料:


  • Chromosome 9p deletion syndrome | About the Disease | GARD
    Monosomy 9p is a chromosome abnormality that occurs when there is a missing (deleted) copy of genetic material on the short arm (p) of chromosome 9 The severity and the signs and symptoms depend on the size and location of the deletion and which genes are involved
  • 9p deletions FTNW - Unique
    People with a break in this region that deletes a so-called ‘critical region’ at 9p22-3 are said to have 9p- or Alfi’s syndrome, named after the geneticist who first identified a group of people with similar features and this specific 9p loss
  • Chromosome 9p Deletion Syndrome - DoveMed
    Learn in-depth information on Chromosome 9p Deletion Syndrome, its causes, symptoms, diagnosis, complications, treatment, prevention, and prognosis
  • chromosome 9p deletion syndrome - National Organization for Rare Disorders
    chromosome 9p deletion syndrome The information provided on this page is for informational purposes only The National Organization for Rare Disorders (NORD) does not endorse the information presented The content has been gathered in partnership with the MONDO Disease Ontology
  • FDNA™ Chromosome 9p deletion: Symptoms, Causes and Diagnosis
    Check your child online and learn about Chromosome 9p deletion syndrome, including its signs, symptoms, diagnosis, and valuable information
  • Entry - #158170 - CHROMOSOME 9p DELETION SYNDROME - OMIM
    In a 2-year-old Japanese boy with clinical characteristics of monosomy 9p syndrome, Kawara et al (2006) identified complex chromosomal rearrangements involving 7 breakpoints in chromosomes 2 and 9, including a 6 6-Mb deletion at 9p23-p22 3
  • Deletion 9p syndrome - OrphanAnesthesia
    In 1976, after identifying three additional patients with the same chromosomal deletion, this group described the deletion 9p syndrome The deletion 9p syndrome is very rare It is estimated to occur in one in 50,000 newborns
  • 9p Deletion Syndrome: Causes, Symptoms, and Diagnosis
    9p deletion syndrome is a rare genetic condition affecting an individual’s development and physical characteristics It occurs due to a missing segment of genetic material on the short arm, or ‘p’ arm, of chromosome 9 Its severity varies depending on the specific genetic material that is absent
  • Distal deletion 9p syndrome - Orphanet
    Patients present an increased risk for gonadoblastoma The documents contained in this website are presented for information purposes only The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment
  • 9p24 deletions FTNW - Unique
    Where part or all of the chromosome between points known as markers D9S285 at 9p22 3 and D9S286 at 9p24 1 has been lost, a syndrome known as 9p- or 9p deletion syndrome occurs (see Unique’s leaflet 9p deletions) When the chromosome has broken in the 9p24 bands, the effects are less certain





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