نتایج جستجو برای: yq ratio

تعداد نتایج: 502303  

Journal: :Journal of medical genetics 1980
J H Priest A T Chen P M Fernhoff J A Reidy C Whitsett

We report a case with non-mosaic Yq-, missing the fluorescent segment, and detected as a fetus studied for advanced maternal age. The father had a Y chromosome of average size and paternity was established wih a plausibility of 97.7% by HLA and erythrocyte antigen typing. The child had a normal male antigen typing. The child had a normal male phenotype at delivery and developmental milestones w...

Journal: :Genomics 1990
E M Fisher T Alitalo S W Luoh A de la Chapelle D C Page

Several categories of human X-Y homologous DNA sequences have been recognized. We report that a locus (DXYS77) approximately 14 kb distal to the pseudoautosomal boundary (PAB) is 93% identical in nucleotide sequence to a locus (DYS148) on the long arm of the Y chromosome (Yq). Within this segment of pseudoautosomal/Yq homology we identified a member of a family of repeats that are concentrated ...

Journal: :Journal of Algebra 2021

We classify irreducible representations of finite W-algebra for the queer Lie superalgebra Q(n) associated with principal nilpotent coadjoint orbits. use this classification and our previous results to obtain a finite-dimensional super Yangian YQ(1).

2012
Bogdan Grzywacz

Finally the paper deals with the solution of the following problem: Let signals y1(iT), ..., yq(iT) (elements of output vector y(iT)) be responses of MIMO discretetime system to the input signals u1(iT),..,uq(iT) (elements of input vector u(iT)). Determine discrete-time excitations uA1,......,uAq (elements of vector uA) scaling the system responses to the required forms y1(iA-1T),...,yq(iA-1T),...

Journal: :Journal of Science and Arts 2020

Journal: :Journal of medical genetics 1999
M Tzancheva R Kaneva P Kumanov G Williams C Tyler-Smith

Turner syndrome is thought to result from the haploinsufficiency of genes on the sex chromosomes, but these genes have not been identified yet. We describe two males with deleted ring Y chromosomes, one (TS) with full Turner syndrome and one (DM) without. TS has short stature, skeletal anomalies, lymphogenic obstruction, cardiovascular abnormalities, and miscellaneous features including pigment...

2013
Jonathan D. Hauenstein Charles W. Wampler

In numerical algebraic geometry, algebraic sets are represented by witness sets. This paper presents an algorithm, based on the regeneration technique, that solves the following problem: given a witness set for a pure-dimensional algebraic set Z, along with a system of polynomial equations f : Z Ñ C, compute a numerical irreducible decomposition of V Z X Vpfq. An important special case is when ...

2017
Delnya Gholami Hamideh Jafari-Ghahfarokhi Maryam Nemati-Dehkordi Hossien Teimori

Background Genetic factors are candidates for about 30% of male infertility with sperm production-related abnormalities. Y chromosome microdeletions are responsible for around 10% of male infertility. These microdeletions generally occur in azoospermia factor on the Yq. That is often associated with the quantitative reduction of sperm. Objective The aim of this cross-sectional study was to de...

Journal: :Human reproduction 2003
C V Hopps A Mielnik M Goldstein G D Palermo Z Rosenwaks P N Schlegel

BACKGROUND Y chromosome microdeletions are associated with severe male factor infertility. In this study, the success rate of testicular sperm retrieval was determined for men with deletions of AZF regions a, b or c. METHODS AZF deletions were detected by PCR of 30 sequence-tagged sites within Yq emphasizing the AZFa, b and c regions. Semen analysis and diagnostic testis biopsy or testicular ...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید