UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

Supernova remnant G46.8–0.3: A new case of interaction with molecular material

Astronomy and astrophysics (Berlin), 2022-08, Vol.664, p.A89

2022

Volltextzugriff (PDF)

Effects of light-emitting diode (led 640nm) on human gingival fibroblasts: a comparative in vitro study

Oral & implantology, 2017-04, Vol.10 (2), p.151-161

2017

Volltextzugriff (PDF)

Incidences and characteristics of injuries during 2011 and 2012 International Athletics Championships

Journal de traumatologie du sport, 2014-03, Vol.31 (1), p.18-27

2014

Volltextzugriff (PDF)

Incidences et caractéristiques des blessures lors des Championnats internationaux d’athlétisme 2011 et 2012

Journal de traumatologie du sport, 2014-03, Vol.31 (1), p.18-27

2014

Volltextzugriff (PDF)

6.5 A new integrated approach for pulmonary veins ablation

Europace (London, England), 2003-10, Vol.4 (Supplement_1), p.A10-A10

2003

Volltextzugriff (PDF)

Construction of an electromagnetic device for the registration of moisture in dental practice

Dental cadmos, 1985-04, Vol.53 (7), p.57-58

1985

Volltextzugriff (PDF)

Production of a device to electronically measure the overheating of teeth undergoing cavity preparation

Dental cadmos, 1984-09, Vol.52 (9 Suppl), p.21-27

1984

Volltextzugriff (PDF)

Cryptic deletions are a common finding in “balanced” reciprocal and complex chromosome rearrangements: a study of 59 patients

Journal of medical genetics, 2007-12, Vol.44 (12), p.750-762

2007

Volltextzugriff (PDF)

Impaired bone remodeling in children with osteogenesis imperfecta treated and untreated with bisphosphonates: the role of DKK1, RANKL, and TNF-α

Osteoporosis international, 2016-07, Vol.27 (7), p.2355-2365

2016

Volltextzugriff (PDF)

Mutations in DONSON disrupt replication fork stability and cause microcephalic dwarfism

Nature genetics, 2017-04, Vol.49 (4), p.537-549

2017

Volltextzugriff (PDF)

Increase in electrical potential induced by composite fillings

Dental cadmos, 1989-04, Vol.57 (7), p.40

1989

Volltextzugriff (PDF)

Mapping the Wolf-Hirschhorn Syndrome Phenotype Outside the Currently Accepted WHS Critical Region and Defining a New Critical Region, WHSCR-2

American journal of human genetics, 2003-03, Vol.72 (3), p.590-597

2003

Volltextzugriff (PDF)

Mutation spectrum of MLL2 in a cohort of Kabuki syndrome patients

Orphanet journal of rare diseases, 2011-06, Vol.6 (1), p.38-38, Article 38

2011

Volltextzugriff (PDF)

Hypomethylation at multiple maternally methylated imprinted regions including PLAGL1 and GNAS loci in Beckwith-Wiedemann syndrome

European journal of human genetics : EJHG, 2009-05, Vol.17 (5), p.611-619

2009

Volltextzugriff (PDF)

A novel microdeletion syndrome at 3q13.31 characterised by developmental delay, postnatal overgrowth, hypoplastic male genitals, and characteristic facial features

Journal of medical genetics, 2012-02, Vol.49 (2), p.104-109

2012

Volltextzugriff (PDF)

Phenotypic spectrum and prevalence of INPP5E mutations in Joubert syndrome and related disorders

European journal of human genetics : EJHG, 2013-10, Vol.21 (10), p.1074-1078

2013

Volltextzugriff (PDF)

Novel homozygous mutation in exon 5 of WFS1 gene in an Apulian family with mild phenotypic expression of Wolfram syndrome

Clinical genetics, 2014-08, Vol.86 (2), p.197-198

2014

Volltextzugriff (PDF)

17β-Hydroxysteroid dehydrogenase-3 deficiency: From pregnancy to adolescence

Journal of endocrinological investigation, 2009-09, Vol.32 (8), p.666-670

2009

Volltextzugriff (PDF)

Nuclear expression of maspin is associated with a lower recurrence rate and a longer disease-free interval after surgery for squamous cell carcinoma of the larynx

Histopathology, 2005-05, Vol.46 (5), p.576-582

2005

Volltextzugriff (PDF)

Mutations in RNF135 , a gene within the NF1 microdeletion region, cause phenotypic abnormalities including overgrowth

Nature genetics, 2007-08, Vol.39 (8), p.963-965

2007

Volltextzugriff (PDF)

Mutation analysis of the NSD1 gene in a group of 59 patients with congenital overgrowth

American journal of medical genetics. Part A, 2005-04, Vol.134A (3), p.247-253

2005

Volltextzugriff (PDF)

RPGRIP1L mutations are mainly associated with the cerebello-renal phenotype of Joubert syndrome-related disorders

Clinical genetics, 2008-08, Vol.74 (2), p.164-170

2008

Volltextzugriff (PDF)

1 – 25 von 38

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(32)
Mit Volltextzugriff
(32)

Publikationsform

Artikel
(37)
Tagungsberichte
(1)

Sprache

Erscheinungsjahr

n.n

Thema

Humans
(29)
Female
(22)
Science & Technology
(22)
Life Sciences & Biomedicine
(21)
Genetics & Heredity
(19)
Male
(19)
Child
(13)
Biological And Medical Sciences
(12)
Medical Sciences
(12)
Child, Preschool
(11)
Phenotype
(9)
Syndrome
(9)
Abnormalities, Multiple - Genetics
(8)
Adult
(8)
Dna Mutational Analysis
(8)
Medical Genetics
(8)
Mutation
(7)
Fundamental And Applied Biological Sciences. Psychology
(6)
Genetics Of Eukaryotes. Biological And Molecular Evolution
(6)
Infant
(6)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Supernova remnant G46.8–0.3: A new case of interaction with molecular material

Effects of light-emitting diode (led 640nm) on human gingival fibroblasts: a comparative in vitro study

Incidences and characteristics of injuries during 2011 and 2012 International Athletics Championships

Incidences et caractéristiques des blessures lors des Championnats internationaux d’athlétisme 2011 et 2012

6.5 A new integrated approach for pulmonary veins ablation

Construction of an electromagnetic device for the registration of moisture in dental practice

Production of a device to electronically measure the overheating of teeth undergoing cavity preparation

Cryptic deletions are a common finding in “balanced” reciprocal and complex chromosome rearrangements: a study of 59 patients

Impaired bone remodeling in children with osteogenesis imperfecta treated and untreated with bisphosphonates: the role of DKK1, RANKL, and TNF-α

Mutations in DONSON disrupt replication fork stability and cause microcephalic dwarfism

Increase in electrical potential induced by composite fillings

Mapping the Wolf-Hirschhorn Syndrome Phenotype Outside the Currently Accepted WHS Critical Region and Defining a New Critical Region, WHSCR-2

Mutation spectrum of MLL2 in a cohort of Kabuki syndrome patients

Hypomethylation at multiple maternally methylated imprinted regions including PLAGL1 and GNAS loci in Beckwith-Wiedemann syndrome

Novel TMEM67 mutations and genotype-phenotype correlates in meckelin-related ciliopathies

A novel microdeletion syndrome at 3q13.31 characterised by developmental delay, postnatal overgrowth, hypoplastic male genitals, and characteristic facial features

Phenotypic spectrum and prevalence of INPP5E mutations in Joubert syndrome and related disorders

Novel homozygous mutation in exon 5 of WFS1 gene in an Apulian family with mild phenotypic expression of Wolfram syndrome

17β-Hydroxysteroid dehydrogenase-3 deficiency: From pregnancy to adolescence

Nuclear expression of maspin is associated with a lower recurrence rate and a longer disease-free interval after surgery for squamous cell carcinoma of the larynx

CEP290 Mutations Are Frequently Identified in the Oculo-Renal Form of Joubert Syndrome–Related Disorders

MKS3/TMEM67 mutations are a major cause of COACH Syndrome, a Joubert Syndrome related disorder with liver involvement

Mutations in RNF135 , a gene within the NF1 microdeletion region, cause phenotypic abnormalities including overgrowth

Mutation analysis of the NSD1 gene in a group of 59 patients with congenital overgrowth

RPGRIP1L mutations are mainly associated with the cerebello-renal phenotype of Joubert syndrome-related disorders

Suchergebnisse filtern