elasticum造句
例句与造句
- Pseudoxanthoma elasticum ( PXE ) is worth consideration in diagnosing a patient.
- It has also been implicated as cofactor in pseudoxanthoma elasticum.
- One group of supporters has applied for patents on a gene that causes the distressing disease pseudoxanthoma elasticum.
- Hi-I went to visit the page on Pseudoxanthoma Elasticum to see what condition it was in.
- "As soon as he looked at it, he said, ` pseudoxanthoma elasticum, "'
- It's difficult to find elasticum in a sentence. 用elasticum造句挺难的
- 80 % of clinical cases of pseudoxanthoma elasticum have detectable mutations in the " ABCC6 " gene.
- Pseudoxanthoma elasticum, myopia and trauma can also cause defects in Bruch's membrane which may lead to choroidal neovascularization.
- Their efforts contributed to significant scientific advances, including the discovery of the gene responsible for Pseudoxanthoma elasticum ( PXE ).
- Rather, peri-mortem submersion resulted in buoyancy that enabled the Ligamentum elasticum to pull the head and tail back.
- It might ultimately snub the small market : This disease, known as pseudoxanthoma elasticum, or PXE, strikes no more than 1 in 25, 000.
- She is a health advocate in Washington, D . C . She co-founded PXE International when her children were diagnosed with pseudoxanthoma elasticum ( PXE ) in 1994.
- In a culmination of concerted efforts initiated by one determined family, three groups of researchers are reporting that they have found the gene mutation that causes a rare disorder known as pseudoxanthoma elasticum.
- There have also been reports in other genetic conditions, such as autosomal dominant polycystic kidney disease and pseudoxanthoma elasticum, Genetic studies in other connective tissue-related genes have mostly yielded negative results.
- When I took a look at the Talk page, I saw a claim that the author had copyrighted the article : http : / / en . wikipedia . org / wiki / Talk : Pseudoxanthoma _ elasticum
- Buschke-Ollendorff syndrome, Menkes disease, pseudoxanthoma elasticum, and Marfan's syndrome have been associated with defects in copper metabolism and lysyl oxidase or defects in the microfibril ( defects in fibrillin, or fibullin for example ).
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