ataxia telangiectasia造句

例句与造句

1. The gene is called ATM ( for ataxia telangiectasia mutated ).
2. Another condition, the gene for which was discovered earlier this year, is ataxia telangiectasia.
3. One of the hallmarks of ataxia telangiectasia is that cells of patients are extremely sensitive to radiation.
4. It may also function in the suppression of radiosensitivity since it is associated with ataxia telangiectasia phenotype.
5. CHD4 has been shown to interact with HDAC1, Histone deacetylase 2, MTA2, and Ataxia telangiectasia and Rad3 related.
6. It's difficult to find ataxia telangiectasia in a sentence. 用ataxia telangiectasia造句挺难的
7. The inherited neurological disorders Machado Joseph disease, ataxia telangiectasia, and Friedreich's ataxia cause progressive neurodegeneration linked to cerebellar loss.
8. These include ataxia telangiectasia, Nijmegen breakage syndrome, some subgroups of xeroderma pigmentosum, trichothiodystrophy, Fanconi anemia, Bloom syndrome and Rothmund-Thomson syndrome.
9. One of Charves's daughters has ataxia telangiectasia, a deadly genetic disease that afflicts only about 650 children in the United States.
10. There is an increased incidence in people with Down syndrome, Fanconi anemia, Bloom syndrome, ataxia telangiectasia, X-linked agammaglobulinemia, and severe combined immunodeficiency.
11. The defect also causes a rare and fatal childhood disease called AT ( ataxia telangiectasia ), which affects neurological and immune function.
12. Examples of autosomal recessive cancer syndromes are ataxia telangiectasia, Bloom syndrome, Fanconi anemia, MUTYH-associated polyposis, Rothmund-Thomson syndrome, Werner's syndrome and Xeroderma pigmentosum.
13. These are ataxia with oculomotor apraxia type 1 ( AOA1 ), ataxia with oculomotor apraxia 2 ( AOA2 ), and ataxia telangiectasia.
14. Patients with ataxia telangiectasia have prolonged vertical and horizontal saccade latencies and hypometric saccades, and, although not all, some patients show head thrusts,.
15. Ataxia telangiectasia ( AT ) is a rare human disease characterized by cerebellar degeneration, extreme cellular sensitivity to radiation and a predisposition to cancer.
16. Mutations in ATR are responsible for Seckel syndrome, a rare human disorder that shares some characteristics with ataxia telangiectasia, which results from ATM mutation.
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