Katalog der Deutschen Nationalbibliothek

Expertensuche ?

Servicezeiten in Frankfurt am Main ab 1. Dezember 2025: Montag bis Freitag 9–18 Uhr und Samstag 10–16 Uhr
Service hours in Frankfurt am Main from 1 December 2025: Monday to Friday 9:00-18:00 and Saturday 10:00-16:00

Leichte Bedienung, intuitive Suche: Die Betaversion unseres neuen Katalogs ist online! → Zur Betaversion des neuen DNB-Katalogs

Ergebnis der Suche nach: "11276925X"
im Bestand: Gesamter Bestand

91 - 100 von 110

	91	Exome Pool-Seq in neurodevelopmental disorders Enthalten in European journal of human genetics Bd. 25, 20.11.2017, Nr. 12, date:12.2017: 1364-1376
	92	Expanding the clinical spectrum associated with defects in CNTNAP2 and NRXN1 Enthalten in BMC medical genetics Bd. 12, 9.8.2011, Nr. 1, date:12.2011: 1-12
	93	Expanding the clinical spectrum of COL1A1 mutations in different forms of glaucoma Enthalten in Orphanet journal of rare diseases Bd. 11, 2.8.2016, Nr. 1, date:12.2016: 1-12
	94	Genome sequencing in families with congenital limb malformations Enthalten in Human genetics Bd. 140, 22.6.2021, Nr. 8, date:8.2021: 1229-1239
	95	Genome-wide association and targeted analysis of copy number variants with psoriatic arthritis in German patients Enthalten in BMC medical genetics Bd. 18, 23.8.2017, Nr. 1, date:12.2017: 1-10
	96	GPFrontend and GPGraphics: graphical analysis tools for genetic association studies Enthalten in BMC bioinformatics Bd. 11, 21.9.2010, Nr. 1, date:12.2010: 1-5
	97	GWAS meta-analysis of psoriasis identifies new susceptibility alleles impacting disease mechanisms and therapeutic targets Enthalten in Nature Communications Bd. 16, 28.2.2025, Nr. 1, date:12.2025: 1-14
	98	Identification of low-frequency TRAF3IP2 coding variants in psoriatic arthritis patients and functional characterization Enthalten in Arthritis Research & Therapy Bd. 14, 18.4.2012, Nr. 2, date:4.2012: 1-5
	99	Identification of the variant Ala335Val of MED25 as responsible for CMT2B2: molecular data, functional studies of the SH3 recognition motif and correlation between wild-type MED25 and PMP22 RNA levels in CMT1A animal models Enthalten in Neurogenetics Bd. 10, 3.9.2009, Nr. 4, date:10.2009: 375-376
	100	Identification of the variant Ala335Val of MED25 as responsible for CMT2B2: molecular data, functional studies of the SH3 recognition motif and correlation between wild-type MED25 and PMP22 RNA levels in CMT1A animal models Enthalten in Neurogenetics Bd. 10, 17.3.2009, Nr. 4, date:10.2009: 275-287

91 - 100 von 110

Alle Materialarten > Artikel (110)

Alle Standorte

Aktionen

Administration