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UnknownGeochemical evolution of dissolved trace elements in space and time in the Ramganga River, India.
Not available
S-EPMC10480240 | biostudies-literature
UnknownHHV-8-unrelated primary effusion-like lymphoma associated with clonal loss of inherited chromosomally-integrated human herpesvirus-6A from the telomere of chromosome 19q.
Not available
S-EPMC4779988 | biostudies-literature
UnknownCorrelation between pseudotyped virus and authentic virus neutralisation assays, a systematic review and meta-analysis of the literature.
Not available
S-EPMC10544934 | biostudies-literature
UnknownDiscovery and SAR of Novel 2,3-Dihydroimidazo[1,2-c]quinazoline PI3K Inhibitors: Identification of Copanlisib (BAY 80-6946).
Not available
S-EPMC5094563 | biostudies-literature
Unknown100,000 Genomes Pilot on Rare-Disease Diagnosis in Health Care - Preliminary Report.
Not available
S-EPMC7613219 | biostudies-literature
UnknownThe Human Phenotype Ontology project: linking molecular biology and disease through phenotype data.
Not available
S-EPMC3965098 | biostudies-literature
UnknownDe Novo SOX6 Variants Cause a Neurodevelopmental Syndrome Associated with ADHD, Craniosynostosis, and Osteochondromas.
Not available
S-EPMC7273536 | biostudies-literature
UnknownCraniosynostosis, inner ear, and renal anomalies in a child with complete loss of <i>SPRY1</i> (sprouty homolog 1) function.
Not available
S-EPMC10359576 | biostudies-literature
UnknownConclusion of diagnostic odysseys due to inversions disrupting <i>GLI3</i> and <i>FBN1</i>.
Not available
S-EPMC10176330 | biostudies-literature
UnknownEvaluating the performance of a clinical genome sequencing program for diagnosis of rare genetic disease, seen through the lens of craniosynostosis.
Not available
S-EPMC8629760 | biostudies-literature
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