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...

Thyroid cancer susceptibility polymorphisms: confirmation of loci on chromosomes 9q22 and 14q13, validation of a recessive 8q24 locus and failure to replicate a locus on 5q24

Journal of medical genetics, 2012-03, Vol.49 (3), p.158-163

2012

Volltextzugriff (PDF)

Genomic imbalances associated with müllerian aplasia

Journal of medical genetics, 2008-04, Vol.45 (4), p.228-232

2008

Volltextzugriff (PDF)

Status of the p53, p16, RB1, and HER-2 genes and chromosomes 3, 7, 9, and 17 in advanced bladder cancer: correlation with adjacent mucosa and pathological parameters

Journal of clinical pathology, 2005-04, Vol.58 (4), p.367-371

2005

Volltextzugriff (PDF)

Psoriasis is associated with pleiotropic susceptibility loci identified in type II diabetes and Crohn disease

Journal of medical genetics, 2008-02, Vol.45 (2), p.114-116

2008

Volltextzugriff (PDF)

Array painting: a method for the rapid analysis of aberrant chromosomes using DNA microarrays

Journal of medical genetics, 2003-09, Vol.40 (9), p.664-670

2003

Volltextzugriff (PDF)

Genomewide linkage scan of hand osteoarthritis in female twin pairs showing replication of quantitative trait loci on chromosomes 2 and 19

Annals of the rheumatic diseases, 2007-05, Vol.66 (5), p.623-627

2007

Volltextzugriff (PDF)

Chromosome 4 hyperploidy represents an early genetic aberration in premalignant Barrett’s oesophagus

Gut, 2003-05, Vol.52 (5), p.623-628

2003

Volltextzugriff (PDF)

Identification of novel candidate genes associated with cleft lip and palate using array comparative genomic hybridisation

Journal of medical genetics, 2008-02, Vol.45 (2), p.81-86

2008

Volltextzugriff (PDF)

Subtelomeric rearrangements detected by FISH in three of 33 families with idiopathic mental retardation and minor physical anomalies

Journal of medical genetics, 2002-09, Vol.39 (9), p.e53-53

2002

Volltextzugriff (PDF)

The genetic basis of Parkinson's disease

Journal of Neurology, Neurosurgery and Psychiatry, 2002-10, Vol.73 (4), p.363-370

2002

Volltextzugriff (PDF)

Stable non-Robertsonian dicentric chromosomes: four new cases and a review

Journal of medical genetics, 2001-01, Vol.38 (1), p.76-79

2001

Volltextzugriff (PDF)

Genome-wide profiling is a clinically relevant and affordable prognostic test in posterior uveal melanoma

British journal of ophthalmology, 2014-06, Vol.98 (6), p.769-774

2014

Volltextzugriff (PDF)

Cytogenetic and molecular study of a jumping translocation in a baby with Dandy-Walker malformation

Journal of medical genetics, 2001-01, Vol.38 (1), p.67-73

2001

Volltextzugriff (PDF)

Molecular-genetic characterisation of gliomas that recur as same grade or higher grade tumours

Journal of neurology, neurosurgery and psychiatry, 2004-05, Vol.75 (5), p.723-726

2004

Volltextzugriff (PDF)

Lymphoma associated chromosomal abnormalities can easily be detected by FISH on tissue imprints. An underused diagnostic alternative

Journal of clinical pathology, 2005-06, Vol.58 (6), p.629-633

2005

Volltextzugriff (PDF)

Epigenotype–phenotype correlations in Silver–Russell syndrome

Journal of medical genetics, 2010-11, Vol.47 (11), p.760-768

2010

Volltextzugriff (PDF)

“Molecular rulers” for calibrating phenotypic effects of telomere imbalance

Journal of medical genetics, 2002-10, Vol.39 (10), p.734-740

2002

Volltextzugriff (PDF)

The genetic aetiology of Silver–Russell syndrome

Journal of medical genetics, 2008-04, Vol.45 (4), p.193-199

2008

Volltextzugriff (PDF)

A genome wide linkage analysis in Swedish families with hereditary non-familial adenomatous polyposis/non-hereditary non-polyposis colorectal cancer

Gut, 2006-03, Vol.55 (3), p.362-366

2006

Volltextzugriff (PDF)

Investigation of the association of Vogt–Koyanagi–Harada syndrome with IL23R-C1orf141 in Han Chinese Singaporean and ADO-ZNF365-EGR2 in Thai

British journal of ophthalmology, 2016-03, Vol.100 (3), p.436-442

2016

Volltextzugriff (PDF)

Silver-Russell syndrome: a dissection of the genetic aetiology and candidate chromosomal regions

Journal of Medical Genetics, 2001-12, Vol.38 (12), p.810-819

2001

Volltextzugriff (PDF)

Constitutional translocation breakpoint mapping by genome-wide paired-end sequencing identifies HACE1 as a putative Wilms tumour susceptibility gene

Journal of medical genetics, 2010-05, Vol.47 (5), p.342-347

2010

Volltextzugriff (PDF)

Identification of clinically significant, submicroscopic chromosome alterations and UPD in fetuses with ultrasound anomalies using genome-wide 250k SNP array analysis

Journal of medical genetics, 2010-09, Vol.47 (9), p.586-594

2010

Volltextzugriff (PDF)

Retinal mosaicism in a girl with an X–Y translocation

British journal of ophthalmology, 2013-02, Vol.97 (2), p.243-243

2013

Volltextzugriff (PDF)

Molecular cytogenetic characterisation of a complex 46,XY,t(7;8;11;13) chromosome rearrangement in a patient with Moebius syndrome

Journal of medical genetics, 2001-02, Vol.38 (2), p.117-120

2001

Volltextzugriff (PDF)

1 – 25 von 4.666

Suche als RSS-Feed

Aktive Filter

KollektionBMJ Journals Archiv - DFG Nationallizenzen

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(4.666)
Mit Volltextzugriff
(4.475)

Publikationsform

Artikel
(4.666)

Sprache

Englisch
(4.666)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Kollektion

EZB Electronic Journals Library
(4.666)
Journals@Ovid Ovid Full Text
(4.666)
BMJ journals single titles
(4.666)
MEDLINE
(4.658)
Publisher or Other Site
(458)
JSTOR All Journals
(39)
Oxford University Press Journals Current
(32)
IngentaConnect
(6)
Wiley Online Library - AutoHoldings Journals
(4)

4 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

Journal Of Medical Genetics
(3.384)
Journal Of Clinical Pathology
(259)
Journal Of Neurology, Neurosurgery And Psychiatry
(257)
Archives Of Disease In Childhood
(200)
British Journal Of Ophthalmology
(146)
J Med Genet
(130)
Gut
(128)
Annals Of The Rheumatic Diseases
(104)
Heart
(54)
Postgraduate Medical Journal
(32)

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

Thyroid cancer susceptibility polymorphisms: confirmation of loci on chromosomes 9q22 and 14q13, validation of a recessive 8q24 locus and failure to replicate a locus on 5q24

Genomic imbalances associated with müllerian aplasia

Status of the p53, p16, RB1, and HER-2 genes and chromosomes 3, 7, 9, and 17 in advanced bladder cancer: correlation with adjacent mucosa and pathological parameters

Psoriasis is associated with pleiotropic susceptibility loci identified in type II diabetes and Crohn disease

Array painting: a method for the rapid analysis of aberrant chromosomes using DNA microarrays

Genomewide linkage scan of hand osteoarthritis in female twin pairs showing replication of quantitative trait loci on chromosomes 2 and 19

Chromosome 4 hyperploidy represents an early genetic aberration in premalignant Barrett’s oesophagus

Identification of novel candidate genes associated with cleft lip and palate using array comparative genomic hybridisation

Subtelomeric rearrangements detected by FISH in three of 33 families with idiopathic mental retardation and minor physical anomalies

The genetic basis of Parkinson's disease

Stable non-Robertsonian dicentric chromosomes: four new cases and a review

Genome-wide profiling is a clinically relevant and affordable prognostic test in posterior uveal melanoma

Cytogenetic and molecular study of a jumping translocation in a baby with Dandy-Walker malformation

Molecular-genetic characterisation of gliomas that recur as same grade or higher grade tumours

Lymphoma associated chromosomal abnormalities can easily be detected by FISH on tissue imprints. An underused diagnostic alternative

Epigenotype–phenotype correlations in Silver–Russell syndrome

“Molecular rulers” for calibrating phenotypic effects of telomere imbalance

The genetic aetiology of Silver–Russell syndrome

A genome wide linkage analysis in Swedish families with hereditary non-familial adenomatous polyposis/non-hereditary non-polyposis colorectal cancer

Investigation of the association of Vogt–Koyanagi–Harada syndrome with IL23R-C1orf141 in Han Chinese Singaporean and ADO-ZNF365-EGR2 in Thai

Silver-Russell syndrome: a dissection of the genetic aetiology and candidate chromosomal regions

Constitutional translocation breakpoint mapping by genome-wide paired-end sequencing identifies HACE1 as a putative Wilms tumour susceptibility gene

Identification of clinically significant, submicroscopic chromosome alterations and UPD in fetuses with ultrasound anomalies using genome-wide 250k SNP array analysis

Retinal mosaicism in a girl with an X–Y translocation

Molecular cytogenetic characterisation of a complex 46,XY,t(7;8;11;13) chromosome rearrangement in a patient with Moebius syndrome

Aktive Filter

Suchergebnisse filtern