Results 131 to 140 of about 12,237 (188)

Chromosomal Microarray Analysis in Spina Bifida: Genetic Heterogeneity and Its Clinical Implications.

J Indian Assoc Pediatr Surg
Pandey H, Sharma J, Kumar S, Mohan N, Jain V, Dhua AK, Yadav DK, Dubey AK, Choudhury P, Goel P.   +9 more
europepmc   +1 more source

An adaptive semantic retrieval framework for digital libraries integrating graph neural networks, ontology, and user behavior. [PDF]

Sci Rep
Bi R.
europepmc   +1 more source

YSO ja LCSH – asiasanastojen uudistukset kertovat arvojen muutoksesta

Asiasanastot kertovat kulttuurisista, yhteiskunnallista ja teknologista ilmiöistä ja muutoksista, mikä näkyy myös Yleisen suomalaisen ontologian (YSO) ja Yhdysvaltain kongressin kirjaston asiasanastojen (LCSH) kehityksessä. Kesäkuussa Finto-palvelun johtavana tietoasiantuntijana aloittaneen Mona Lehtisen mukaan YSOn kehittäminen vaatii ...
openaire   +1 more source

An integrated analysis tool for analyzing hybridization intensities and genotypes using new-generation population-optimized human arrays. [PDF]

BMC Genomics, 2016
Huang MC, Chuang TP, Chen CH, Wu JY, Chen YT, Li LH, Yang HC.   +6 more
europepmc   +1 more source

Imenovani entiteti u predmetnom označivanju : LCSH i Nuovo soggettario

Vjesnik Bibliotekara Hrvatske, 2015
Ana Vukadin
doaj  

The Diagnostic Utility of Single Long Contiguous Stretches of Homozygosity in Patients without Parental Consanguinity. [PDF]

Mol Syndromol, 2015
Pajusalu S, Žilina O, Yakoreva M, Tammur P, Kuuse K, Mölter-Väär T, Nõukas M, Reimand T, Õunap K.   +8 more
europepmc   +1 more source

Decreased calcium permeability caused by biallelic TRPV5 mutation leads to autosomal recessive renal calcium-wasting hypercalciuria. [PDF]

Eur J Hum Genet
Guleray Lafci N, van Goor M, Cetinkaya S, van der Wijst J, Acun M, Kurt Colak F, Cetinkaya A, Hoenderop J.   +7 more
europepmc   +1 more source

Automatic Assignment of LCSH : Combining Classification and Extraction

, 2017
Wartena, Christian, Franke-Maier, Michael   +1 more
openaire   +3 more sources

SNP Analysis and Whole Exome Sequencing: Their Application in the Analysis of a Consanguineous Pedigree Segregating Ataxia. [PDF]

Microarrays (Basel), 2015
Nickerson SL, Marquis-Nicholson R, Claxton K, Ashton F, Leong IU, Prosser DO, Love JM, George AM, Taylor G, Wilson C, Gardner RJ, Love DR.   +11 more
europepmc   +1 more source

The Cytoscan HD Array in the Diagnosis of Neurodevelopmental Disorders. [PDF]

High Throughput, 2018
Scionti F, Di Martino MT, Pensabene L, Bruni V, Concolino D.   +4 more
europepmc   +1 more source