Results 111 to 120 of about 1,010 (181)

A Study on the Development of Topical Headings Related to Korea in LCSH

open access: yesJournal of Korean Library and Information Science Society, 2009
null KimJeonghyen, null 문지현
openaire   +1 more source

Imenovani entiteti u predmetnom označivanju : LCSH i Nuovo soggettario

open access: yesVjesnik Bibliotekara Hrvatske, 2015
Ana Vukadin
doaj  

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

open access: yesMol Syndromol, 2015
Pajusalu S   +8 more
europepmc   +1 more source

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

open access: yesEur J Hum Genet
Guleray Lafci N   +7 more
europepmc   +1 more source

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

open access: yesMicroarrays (Basel), 2015
Nickerson SL   +11 more
europepmc   +1 more source

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

open access: yesHigh Throughput, 2018
Scionti F   +4 more
europepmc   +1 more source

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