Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Zhanhe, Wu"'
Publikováno v:
Frontiers in Physics, Vol 10 (2022)
Many researchers propose link prediction models based on node similarity. Among all models, researchers found that the endpoint influence plays an important role in evaluating the similarity between endpoints. For endpoint influence, we consider that
Externí odkaz:
https://doaj.org/article/9b9266a22c0946c6a171c8c82170ca11
Publikováno v:
IOP Conference Series: Earth and Environmental Science. 632:042072
The realization of the full coverage of the smart meter and the metering automation terminal across the entire network brings great challenges to the operation and maintenance of the field. Aiming at the long-term problems of on-site failure operatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2fd7c6e0b964730742874ad4f22b629d
https://doi.org/10.1088/1755-1315/632/4/042072
https://doi.org/10.1088/1755-1315/632/4/042072
Autor:
Zhanhe Wu
As defined initially, chromosome instability syndromes (CIS) are a group of inherited conditions transmitted in autosomal recessive pattern characterised with both mental and physical development delay generally. They are also with other medical comp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::56af0a7d594d786136f98bcc884ef7f1
https://europepmc.org/articles/PMC4855194/
https://europepmc.org/articles/PMC4855194/
Autor:
Zhanhe, Wu
Publikováno v:
Translational pediatrics. 4(3)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::fa1131bec4aaec2c1e4eea64ef0a1f68
https://pubmed.ncbi.nlm.nih.gov/26835381
https://pubmed.ncbi.nlm.nih.gov/26835381
Publikováno v:
Translational pediatrics. 3(2)
Spectral karyotyping (SKY) is a novel cytogenetic technique, has been developed to unambiguously display and identify all 24 humans chromosomes at one time without a priori knowledge of any abnormalities involved. SKY can discern the aberrations that
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::aa0d31434ac449e6df27d779540e18e0
https://pubmed.ncbi.nlm.nih.gov/26835331
https://pubmed.ncbi.nlm.nih.gov/26835331
Publikováno v:
Translational pediatrics. 3(4)
Fanconi anemia (FA) is a recessive chromosomal instability syndrome. It is a hereditary disorder with defects in DNA repair characterized by progressive bone marrow failure, variable congenital malformations and predisposition to develop hematologica
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::67b996f247eb09b5afaa026d1b48bd47
https://pubmed.ncbi.nlm.nih.gov/26835350
https://pubmed.ncbi.nlm.nih.gov/26835350
Publikováno v:
Translational pediatrics. 3(2)
Hereditary neurological disorders (HNDs) are relatively common in children compared to those occurring in adulthood. Recognising clinical manifestations of HNDs is important for the selection of genetic testing, genetic testing results interpretation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c2362c3d302e32935f9bcb2165e740d9
https://pubmed.ncbi.nlm.nih.gov/26835329
https://pubmed.ncbi.nlm.nih.gov/26835329
Publikováno v:
Translational pediatrics. 3(4)
The inherited bone marrow failure syndromes (IBMFS) are a rare group of heterogeneous genetic disorders characterised by bone marrow failure, commonly associated with one or more congenital anomalies found in patients which have a familiar predisposi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5e160fe0a74f782f38c6ba36081a9fd4
https://pubmed.ncbi.nlm.nih.gov/26835351
https://pubmed.ncbi.nlm.nih.gov/26835351
Publikováno v:
Translational pediatrics. 3(2)
Plasma DNA has had a strong impact and influence on basic medical research and clinical practice since the discovery of low levels of plasma DNA in healthy individuals under different physiological conditions. Although the source of circulating DNA s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3584c6b86ef36307ea4b8207d7cf6968
https://pubmed.ncbi.nlm.nih.gov/26835332
https://pubmed.ncbi.nlm.nih.gov/26835332
Publikováno v:
Prenatal Diagnosis. 27:1197-1204
Objective To evaluate the ability of a DNA single nucleotide polymorphism (SNP) microarray to detect chromosome mosaicism for trisomy in prenatal samples in order to compare this with conventional cytogenetics. Method We created a dilution series of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7371473bc30a2bfa090a1502c8f82a1c
https://doi.org/10.1002/pd.1884
https://doi.org/10.1002/pd.1884