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...

LQTS in Northern BC: homozygosity for KCNQ1 V205M presents with a more severe cardiac phenotype but with minimal impact on auditory function

Clinical genetics, 2014-07, Vol.86 (1), p.85-90

2014

Volltextzugriff (PDF)

Pre‐eclampsia and risk of infantile haemangioma

British journal of dermatology (1951), 2017-02, Vol.176 (2), p.371-377

2017

Volltextzugriff (PDF)

Genomic Research Through an Indigenous Lens: Understanding the Expectations

Annual review of genomics and human genetics, 2019-08, Vol.20 (1), p.495-517

2019

Volltextzugriff (PDF)

Association Between Preeclampsia and Congenital Heart Defects

Obstetric anesthesia digest, 2016-09, Vol.36 (3), p.135-136

2016

Volltextzugriff (PDF)

565 Systemic lupus erythematosus patients in a first nations community of northern British Columbia exhibit an elevated QT interval when compared to individuals negative for the KCNQ1 V205M missense mutation conferring predisposition to long QT syndrome

Canadian journal of cardiology, 2011-09, Vol.27 (5), p.S266-S266

2011

Volltextzugriff (PDF)

Submicroscopic deletions and duplications in individuals with intellectual disability detected by array-CGH

American journal of medical genetics. Part A, 2005-12, Vol.139A (3), p.173-185

2005

Volltextzugriff (PDF)

Silver-Catalysed Enantioselective Addition of OH and NH Bonds to Allenes: A New Model for Stereoselectivity Based on Noncovalent Interactions

Chemistry : a European journal, 2012-09, Vol.18 (36), p.11317-11324

2012

Volltextzugriff (PDF)

THE BC INHERITED ARRHYTHMIA PROGRAM: A MULTIDISCIPLINARY APPROACH TO FAMILIES AT RISK FOR SUDDEN DEATH

Canadian journal of cardiology, 2014-10, Vol.30 (10), p.S300-S300

2014

Volltextzugriff (PDF)

A MILD PHENOTYPE ASSOCIATED WITH KCNQ1 P.V205M MEDIATED LONG QT SYNDROME IN FIRST NATIONS CHILDREN OF NORTHERN BRITISH COLUMBIA: EFFECT OF ADDITIONAL VARIANTS AND CONSIDERATIONS FOR MANAGEMENT

Canadian journal of cardiology, 2023-10, Vol.39 (10), p.S30-S31

2023

Volltextzugriff (PDF)

A MILD PHENOTYPE ASSOCIATED WITH KCNQ1 P.V205M MEDIATED LONG QT SYNDROME IN FIRST NATIONS CHILDREN OF NORTHERN BRITISH COLUMBIA: EFFECT OF ADDITIONAL VARIANTS AND CONSIDERATIONS FOR MANAGEMENT

Canadian journal of diabetes, 2023-11, Vol.47 (7), p.S11-S12

2023

Volltextzugriff (PDF)

Unusual regiodivergence in metal-catalysed intramolecular cyclisation of gamma-allenols

Chemical communications (Cambridge, England), 2009-01 (46), p.7125-7127

2009

Volltextzugriff (PDF)

Prenatally detected trisomy 20 mosaicism

Prenatal diagnosis, 2005-03, Vol.25 (3), p.239-244

2005

Volltextzugriff (PDF)

HIGH RISK NON-CLASSICAL LQTS GENOTYPES: SPECTRUM OF GENETIC AND PHENOTYPIC FEATURES OF LONG QT SYNDROME

Canadian journal of cardiology, 2023-10, Vol.39 (10), p.S48-S49

2023

Volltextzugriff (PDF)

PHENOTYPIC DIFFERENCES BETWEEN "COMMON” LONG QT TYPE 1 VARIANT CARRIERS IN THE NATIONAL HIRO REGISTRY

Canadian journal of cardiology, 2023-10, Vol.39 (10), p.S53-S54

2023

Volltextzugriff (PDF)

Evidence for a familial Wilms' tumour gene ( FWT1 ) on chromosome 17q12-q21

Nature genetics, 1996-08, Vol.13 (4), p.461-463

1996

Volltextzugriff (PDF)

DNA on Loan: Issues to Consider when Carrying Out Genetic Research with Aboriginal Families and Communities

Community genetics, 2006-01, Vol.9 (3), p.153-160

2006

Volltextzugriff (PDF)

A190 POST-PARTUM PRIMARY BILIARY CHOLANGITIS (PBC) AFTER RESOLUTION OF INTRAHEPATIC CHOLESTASIS OF PREGNANCY (ICP) IN FIRST NATION’S PATIENTS OF BC: A CASE SERIES

Journal of the Canadian Association of Gastroenterology, 2020-02, Vol.3 (Supplement_1), p.61-62

2020

Volltextzugriff (PDF)

Constitutional 11p15 abnormalities, including heritable imprinting center mutations, cause nonsyndromic Wilms tumor

Nature genetics, 2008-11, Vol.40 (11), p.1329-1334

2008

Volltextzugriff (PDF)

VARIANT RE-INTERPRETATION IN SURVIVORS OF CARDIAC ARREST WITH PRESERVED EJECTION FRACTION (CASPER REGISTRY) BY CLINICIANS AND CLINICAL COMMERCIAL LABORATORIES

Canadian journal of cardiology, 2020-10, Vol.36 (10), p.S55-S56

2020

Volltextzugriff (PDF)

Recurrent trisomy 21: four cases in three generations

Clinical genetics, 2005-11, Vol.68 (5), p.430-435

2005

Volltextzugriff (PDF)

LONG-TERM ARRHYTHMIC OUTCOMES AMONG CARDIAC ARREST SURVIVORS WITH PRESERVED EJECTION FRACTION REGISTRY (CASPER)

Canadian journal of cardiology, 2021-10, Vol.37 (10), p.S47-S48

2021

Volltextzugriff (PDF)

HIGH RISK NON-CLASSICAL LQTS GENOTYPES: SPECTRUM OF GENETIC AND PHENOTYPIC FEATURES OF LONG QT SYNDROME

Canadian journal of diabetes, 2023-11, Vol.47 (7), p.S27-S27

2023

Volltextzugriff (PDF)

PHENOTYPIC DIFFERENCES BETWEEN "COMMON” LONG QT TYPE 1 VARIANT CARRIERS IN THE NATIONAL HIRO REGISTRY

Canadian journal of diabetes, 2023-11, Vol.47 (7), p.S32-S32

2023

Volltextzugriff (PDF)

Prenatal diagnosis of apparently isolated unilateral multicystic kidney: implications for counselling and management

Prenatal diagnosis, 2002-05, Vol.22 (5), p.388-394

2002

Volltextzugriff (PDF)

1 – 25 von 1.426

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(1.108)
Mit Volltextzugriff
(1.151)

Publikationsform

6 weitere anzeigen...

Weniger anzeigen...

Sprache

2 weitere anzeigen...

Weniger anzeigen...

Erscheinungsjahr

n.n

Thema

Science & Technology
(808)
Physical Sciences
(479)
Physics
(388)
Life Sciences & Biomedicine
(265)
Physics Of Elementary Particles And Fields
(187)
Humans
(178)
Astronomy & Astrophysics
(169)
Astronomy And Astrophysics
(166)
Technology
(127)
Female
(97)
Astrophysics
(96)
Physics, Multidisciplinary
(94)
Animals
(90)
Chemistry
(86)
Physics, Particles & Fields
(86)
Male
(85)
Biological And Medical Sciences
(83)
Instrumentation Related To Nuclear Science And Technology
(77)
Medical Sciences
(64)
70 Plasma Physics And Fusion Technology
(61)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(1)
... seit 90 Tagen
(3)

Menü

Weitere Dienste

Einstellungen

LQTS in Northern BC: homozygosity for KCNQ1 V205M presents with a more severe cardiac phenotype but with minimal impact on auditory function

Pre‐eclampsia and risk of infantile haemangioma

Genomic Research Through an Indigenous Lens: Understanding the Expectations

Association Between Preeclampsia and Congenital Heart Defects

565 Systemic lupus erythematosus patients in a first nations community of northern British Columbia exhibit an elevated QT interval when compared to individuals negative for the KCNQ1 V205M missense mutation conferring predisposition to long QT syndrome

Submicroscopic deletions and duplications in individuals with intellectual disability detected by array-CGH

Silver-Catalysed Enantioselective Addition of OH and NH Bonds to Allenes: A New Model for Stereoselectivity Based on Noncovalent Interactions

THE BC INHERITED ARRHYTHMIA PROGRAM: A MULTIDISCIPLINARY APPROACH TO FAMILIES AT RISK FOR SUDDEN DEATH

A MILD PHENOTYPE ASSOCIATED WITH KCNQ1 P.V205M MEDIATED LONG QT SYNDROME IN FIRST NATIONS CHILDREN OF NORTHERN BRITISH COLUMBIA: EFFECT OF ADDITIONAL VARIANTS AND CONSIDERATIONS FOR MANAGEMENT

A MILD PHENOTYPE ASSOCIATED WITH KCNQ1 P.V205M MEDIATED LONG QT SYNDROME IN FIRST NATIONS CHILDREN OF NORTHERN BRITISH COLUMBIA: EFFECT OF ADDITIONAL VARIANTS AND CONSIDERATIONS FOR MANAGEMENT

Unusual regiodivergence in metal-catalysed intramolecular cyclisation of gamma-allenols

Prenatally detected trisomy 20 mosaicism

Oligonucleotide Microarray Analysis of Genomic Imbalance in Children with Mental Retardation

HIGH RISK NON-CLASSICAL LQTS GENOTYPES: SPECTRUM OF GENETIC AND PHENOTYPIC FEATURES OF LONG QT SYNDROME

PHENOTYPIC DIFFERENCES BETWEEN "COMMON” LONG QT TYPE 1 VARIANT CARRIERS IN THE NATIONAL HIRO REGISTRY

Evidence for a familial Wilms' tumour gene ( FWT1 ) on chromosome 17q12-q21

DNA on Loan: Issues to Consider when Carrying Out Genetic Research with Aboriginal Families and Communities

A190 POST-PARTUM PRIMARY BILIARY CHOLANGITIS (PBC) AFTER RESOLUTION OF INTRAHEPATIC CHOLESTASIS OF PREGNANCY (ICP) IN FIRST NATION’S PATIENTS OF BC: A CASE SERIES

Constitutional 11p15 abnormalities, including heritable imprinting center mutations, cause nonsyndromic Wilms tumor

VARIANT RE-INTERPRETATION IN SURVIVORS OF CARDIAC ARREST WITH PRESERVED EJECTION FRACTION (CASPER REGISTRY) BY CLINICIANS AND CLINICAL COMMERCIAL LABORATORIES

Recurrent trisomy 21: four cases in three generations

LONG-TERM ARRHYTHMIC OUTCOMES AMONG CARDIAC ARREST SURVIVORS WITH PRESERVED EJECTION FRACTION REGISTRY (CASPER)

HIGH RISK NON-CLASSICAL LQTS GENOTYPES: SPECTRUM OF GENETIC AND PHENOTYPIC FEATURES OF LONG QT SYNDROME

PHENOTYPIC DIFFERENCES BETWEEN "COMMON” LONG QT TYPE 1 VARIANT CARRIERS IN THE NATIONAL HIRO REGISTRY

Prenatal diagnosis of apparently isolated unilateral multicystic kidney: implications for counselling and management

Suchergebnisse filtern