نتایج جستجو برای: yq deletions
تعداد نتایج: 19460 فیلتر نتایج به سال:
Background: Plasmodium falciparum histidine rich protein 2/3 gene deletions (Pfhrp2/3gd) threatens usefulness of mRDT in diagnosing malaria cases. This review was performed to assess the methods used report findings on those between January 2010 and December 2021.
 Methods: Present search using Medline, Google Scholar PubMed.
 Results: Out 94 articles identified, 19% (n=18) were inclu...
Abstract Introduction Microdeletions of the Y-chromosome (Yq) and karyotype abnormalities are frequent causes male factor infertility. Current AUA/EUA guidelines recommend obtaining Yq microdeletion analysis, karyotype, genetic counseling in men with non-obstructive azoospermia or severe oligospermia (<5 mil/mL). A recent retrospective cohort study suggests that microdeletions primarily ...
This paper studies the problem of constructing codes correcting deletions in arrays. Under this model, it is assumed that an $n \times n$ array can experience rows and columns. These deletion errors are referred to as notation="LaTeX"...
Let jp „ denote the nth positive zero of J , p > 0. Then / ■■> 7\'/2 Jp.n > Oln + P) ■ We begin by considering the eigenvalue problem (1) -(•*/)' + x~y = X2x2p-Xy, X,p>0, (2) y(a) =y(\) = 0, 0 < a < 1. For simplicity of notation we will set q = p~x. It is easily verified that the general solution of (1) is y(x) = CxJq(Xqxx/q) + C2Yq(Xqxx'q) and that the eigenvalues are given by Jq(Xq)Yq(Xqax/q)...
Homozygous deletions of recessive cancer genes and fragile sites are known to occur in human cancers. We identified 281 homozygous deletions in 636 cancer cell lines. Of these deletions, 86 were homozygous deletions of known recessive cancer genes, 17 were of sequenced common fragile sites, and 178 were in genomic regions that do not overlap known recessive oncogenes or fragile sites ("unexplai...
This paper investigates the problem of correcting multiple criss-cross insertions and deletions in arrays. More precisely, we study unique recovery $n \times n$ arrays affected by notation="LaTeX">${t}$ <italic xmlns:xlink="http://www...
how to cite this article: barzegar m, habibi p, bonyady m, topchizadeh v, shiva sh. exon deletion pattern in duchene muscular dystrophy in north west of iran. iran j child neurol. 2015 winter; 9(1): 42-48. abstract objective duchene and becker muscular dystrophy (dmd/ bmd) are x-linked disorders that both are the result of heterogeneous mutations in the dystrophin gene. the frequency and distri...
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