Genetic profiling of embryos prior to implantation.
Russian
генетический скрининг Catalan
cribratge genètic 1
Here, we present the first genome-wide genetic screen of an apicomplexan.
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We conducted a genetic screen to identify additional components of the endo RNAi machinery.
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A previous forward genetic screen identified 23 A. nidulans mutants involved in regulating ST production.
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From a forward genetic screen, we isolated five mutant lines with reduced innate startle thresholds.
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To study this problem, we performed a genetic screen for larval growth-defective mutants in Drosophila melanogaster.
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Newborn genetic screening and carrier identification were also performed in the family.
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Preimplantation genetic screening is used to detect chromosomal aneuploidies in early embryos.
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These results might contribute to the genetic screening of EOPD in Vietnam.
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Molecular genetic screening confirms the diagnosis and the autosomal recessive inheritance.
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Otherwise, a connection might have been spotted during routine genetic screening using official records.
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Since 1997 the diagnosis can be made by genetic screening.
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Objective: This case highlights the value of genetic screening for idiopathic osteoporosis with recurrent fractures.
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Family history is important in scheduling specific genetic screening in high-risk patients and their relatives.
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The potential for genetic screening of multifactorial diseases, for example, cancers, should also be considered.
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Couples undergoing in vitro fertilization donated the embryos after the clinic performed prenatal genetic screening.
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Would it eventually force the industry itself to resort to a genetic screening-out of certain clients?
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Helping owners interpret and understand results from genetic screening panels is becoming an important issue facing veterinarians.
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Meanwhile, molecular genetic screening can reveal specific mutations of ion channels and can identify consecutive functional defects.
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STR melting curve analysis for genetic screening.
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Before genetic screening, participants were asked whether they had a history of medical conditions related to iron overload.
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The size of such studies often makes it necessary to distribute the genetic screening efforts to multiple sites.
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