autosomal造句
1. Autosomal bivalents can be arranged in order of size, but unambiguous identification of individual bivalents is not possible.
2. This disorder is inherited as an autosomal dominant trait.
3. Citrin deficiency is inherited in an autosomal recessive manner.
4. HHT is an autosomal dominant disordercharacterized by vascular dysplasia.
5. Congenital afibrinogenemia is a rare autosomal recessive disorder, characterized by the complete absence or extremely reduced level of fibrinogen.
6. Objective To elucidate the molecular mechanism of autosomal dominant neurohypophyseal diabetes insipidus in Chinese.
7. Objective To improve the operative treatment of autosomal dominant polycystic kidney disease(ADPKD).
8. Result: ATD is an uncommon autosomal recessive hereditary disorder of osteochondrodysplasia.
9. Epidermolytic palmoplantar keratoderma , a rare autosomal dominant hereditary disease, is a keratinization disorder of palms and soles caused by mutation in the keratin 9 gene.
10. Bovine leukocyte adhesion deficiency ( BLAD ) is autosomal recessive disease. The pathogeny of BLAD is genic mutation of CD18-integrins on the leukocyte.
11. Genetic counseling. Cystinosis is inherited in an autosomal recessive manner.
12. Lipid storage myopathy is one kind of autosomal recessive inherited disease with lipid abnormally sludging in the muscle cell.
13. Objective : To study the relationship between autosomal polymorphism and male infertility.
14. The structural changes that are seen in hemoglobin 5 and C disorders are inherited as autosomal recessive traits. 216.
15. Harlequin ichthyosis ( HI ) is a severe subtype of autosomal recessive congenital ichthyoses ( ARCI ) .
16. Conclusion:The model of inheritance of panic disorder maybe a kind of polygene disease with a recessive major gene or conform to autosomal recessive inheritance.
17. Most mammals hae just two kinds of photopigment in their retinas : one is encoded in the X chromosome and the other in an autosomal (non-sex) chromosome.
18. Objective:To observe the clinical effect of laparoscopic renal cyst decortication in patients with autosomal dominant polycystic kidney disease.
19. Methods We screened a family affected by long-QT syndrome type 1 and identified an autosomal dominant missense mutation (R190Q) in the KCNQ1 gene.
20. We examined three families and suggest that it has an autosomal dominant trait with incomplete penetrance.
21. Conclusion The association of gap junction protein gene with this autosomal dominant congenital pulverulent cataract was preliminary excluded.
22. Objective:To analyze the relationship between the genotype and phenotype of autosomal dominant polycystic kidney disease(ADPKD) in Han nationality in East China.
23. Objective To develop a method for detecting the mutations in autosomal dominant polycystic kidney disease gene 2(PKD2) and detect the mutations of PKD2 in Chinese.
24. Owing to the influence of various complex factors, it is possible for the heterozygote of autosomal dominant inheritance to appear in different phenotypes.
25. Klinefelter syndrome is still the most common chromosomal disease, balanced translocation accounts for largest proportion of autosomal abnormality.
26. Congenital microphthalmia is a developmental defect of ocular disorder with autosomal dominant, autosomal recessive, and X-linked recessive modes of inheritance.
27. However, approximately 30% of IHH is familial and can be inherited in an autosomal dominant , autosomal recessive , or X-linked manner.
28. Objective:Cyst lining epithelial cell proliferation and apoptosis are implicated in the pathogenesis of cyst formation in autosomal dominant polycystic kidney disease(ADPKD).
29. It is shown that the mean relative lengths and centromeric indices of autosomal SCs agree closely with those of mitotic chromosomes.
30. Objective To map the virulence gene for a family with coronary autosomal dominant congenital cataracts ( ADCC ).
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