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...

Genetic counselors and congenital heart disease: Clinical roles, genetic testing practices, and perceived genetic testing utility

Journal of genetic counseling, 2024-10, Vol.33 (5), p.1004-1014

2024

Volltextzugriff (PDF)

A descriptive investigation of clinical practice models used by cardiovascular genetic counselors in North America

Journal of genetic counseling, 2023-04, Vol.32 (2), p.362-375

2023

Volltextzugriff (PDF)

Novel familial dilated cardiomyopathy mutation in MYL2 affects the structure and function of myosin regulatory light chain

The FEBS journal, 2015-06, Vol.282 (12), p.2379-2393

2015

Volltextzugriff (PDF)

Management of amended variant classification laboratory reports by genetic counselors in the United States and Canada: An exploratory study

Journal of genetic counseling, 2022-04, Vol.31 (2), p.479-488

2022

Volltextzugriff (PDF)

Prevalence of De Quervain disease in infant caregivers and its association with risk factors

Journal of the Pakistan Medical Association, 2024-07, Vol.74 (7), p.1335

2024

Volltextzugriff (PDF)

Assessing genetic counselors’ graduate school education and training in congenital heart defects

Journal of genetic counseling, 2022-06, Vol.31 (3), p.735-745

2022

Volltextzugriff (PDF)

Genetic counseling for congenital heart disease – Practice resource of the National Society of Genetic Counselors

Journal of genetic counseling, 2022-02, Vol.31 (1), p.9-33

2022

Volltextzugriff (PDF)

It's not as simple as just bending wires

British dental journal, 2023-09, Vol.235 (5), p.323-323

Butt, Sara

2023

Volltextzugriff (PDF)

Building a Novel Artificial Intelligence–Driven Echocardiographic Data Pipeline: Findings From a Large Learning Health System

Journal of the American Society of Echocardiography, 2024-09, Vol.37 (9), p.916-918

2024

Volltextzugriff (PDF)

NOTCH1 mutations in individuals with left ventricular outflow tract malformations reduce ligand-induced signaling

Human molecular genetics, 2008-09, Vol.17 (18), p.2886-2893

2008

Volltextzugriff (PDF)

ChatGPT and Artificial Intelligence in Hospital Level Research: Potential, Precautions, and Prospects

Methodist DeBakey cardiovascular journal, 2023, Vol.19 (5), p.77-84

2023

Volltextzugriff (PDF)

Lifetime Prevalence of Sexual Intercourse and Contraception Use at Last Sex Among Adolescents and Young Adults With Congenital Heart Disease

Journal of adolescent health, 2015-04, Vol.56 (4), p.396-401

2015

Volltextzugriff (PDF)

Exome sequencing in multiplex families with left-sided cardiac defects has high yield for disease gene discovery

PLoS genetics, 2022-06, Vol.18 (6), p.e1010236-e1010236

2022

Volltextzugriff (PDF)

Genetic knowledge and attitudes of parents of children with congenital heart defects

American journal of medical genetics. Part A, 2014-12, Vol.164A (12), p.3069-3075

2014

Volltextzugriff (PDF)

Understanding of informed consent by parents of children enrolled in a genetic biobank

Genetics in medicine, 2014-02, Vol.16 (2), p.141-148

2014

Volltextzugriff (PDF)

Comparison of willingness and preference for genetic counseling via telemedicine: before vs. during the COVID-19 pandemic

Journal of community genetics, 2022-08, Vol.13 (4), p.449-458

2022

Volltextzugriff (PDF)

The role of breathing techniques in the management of asthma: A systematic review

Journal of the Pakistan Medical Association, 2024-07, Vol.74 (7), p.1296-1299

2024

Volltextzugriff (PDF)

At the Heart of the Pregnancy: What Prenatal and Cardiovascular Genetic Counselors Need to Know about Maternal Heart Disease

Journal of genetic counseling, 2017-08, Vol.26 (4), p.669-688

2017

Volltextzugriff (PDF)

Novel frameshift variant in MYL2 reveals molecular differences between dominant and recessive forms of hypertrophic cardiomyopathy

PLoS genetics, 2020-05, Vol.16 (5), p.e1008639-e1008639

2020

Volltextzugriff (PDF)

A genome-wide association study of congenital cardiovascular left-sided lesions shows association with a locus on chromosome 20

Human molecular genetics, 2016-06, Vol.25 (11), p.2331-2341

2016

Volltextzugriff (PDF)

Association of common variants in ERBB4 with congenital left ventricular outflow tract obstruction defects

Birth defects research. A Clinical and molecular teratology, 2011-03, Vol.91 (3), p.162-168

2011

Volltextzugriff (PDF)

Utilization of Whole Exome Sequencing to Identify Causative Mutations in Familial Congenital Heart Disease

Circulation. Cardiovascular genetics, 2016-08, Vol.9 (4), p.320-329

2016

Volltextzugriff (PDF)

Linkage analysis of left ventricular outflow tract malformations (aortic valve stenosis, coarctation of the aorta, and hypoplastic left heart syndrome)

European journal of human genetics : EJHG, 2009-06, Vol.17 (6), p.811-819

2009

Volltextzugriff (PDF)

Erratum to: At the Heart of the Pregnancy: What Prenatal and Cardiovascular Genetic Counselors Need to Know about Maternal Heart Disease

Journal of genetic counseling, 2017-08, Vol.26 (4), p.689-689

2017

Volltextzugriff (PDF)

Assessment of large copy number variants in patients with apparently isolated congenital left‐sided cardiac lesions reveals clinically relevant genomic events

American journal of medical genetics. Part A, 2017-08, Vol.173 (8), p.2176-2188

2017

Volltextzugriff (PDF)

1 – 25 von 233

Suche als RSS-Feed

Aktive Filter

ThemaAged

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(209)
Mit Volltextzugriff
(192)

Publikationsform

Sprache

Englisch
(233)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(2)
... seit 90 Tagen
(6)

Menü

Weitere Dienste

Einstellungen

Genetic counselors and congenital heart disease: Clinical roles, genetic testing practices, and perceived genetic testing utility

A descriptive investigation of clinical practice models used by cardiovascular genetic counselors in North America

Novel familial dilated cardiomyopathy mutation in MYL2 affects the structure and function of myosin regulatory light chain

Management of amended variant classification laboratory reports by genetic counselors in the United States and Canada: An exploratory study

Prevalence of De Quervain disease in infant caregivers and its association with risk factors

Assessing genetic counselors’ graduate school education and training in congenital heart defects

Genetic counseling for congenital heart disease – Practice resource of the National Society of Genetic Counselors

It's not as simple as just bending wires

Building a Novel Artificial Intelligence–Driven Echocardiographic Data Pipeline: Findings From a Large Learning Health System

NOTCH1 mutations in individuals with left ventricular outflow tract malformations reduce ligand-induced signaling

ChatGPT and Artificial Intelligence in Hospital Level Research: Potential, Precautions, and Prospects

Lifetime Prevalence of Sexual Intercourse and Contraception Use at Last Sex Among Adolescents and Young Adults With Congenital Heart Disease

Exome sequencing in multiplex families with left-sided cardiac defects has high yield for disease gene discovery

Genetic knowledge and attitudes of parents of children with congenital heart defects

Understanding of informed consent by parents of children enrolled in a genetic biobank

Comparison of willingness and preference for genetic counseling via telemedicine: before vs. during the COVID-19 pandemic

The role of breathing techniques in the management of asthma: A systematic review

At the Heart of the Pregnancy: What Prenatal and Cardiovascular Genetic Counselors Need to Know about Maternal Heart Disease

Novel frameshift variant in MYL2 reveals molecular differences between dominant and recessive forms of hypertrophic cardiomyopathy

A genome-wide association study of congenital cardiovascular left-sided lesions shows association with a locus on chromosome 20

Association of common variants in ERBB4 with congenital left ventricular outflow tract obstruction defects

Utilization of Whole Exome Sequencing to Identify Causative Mutations in Familial Congenital Heart Disease

Linkage analysis of left ventricular outflow tract malformations (aortic valve stenosis, coarctation of the aorta, and hypoplastic left heart syndrome)

Erratum to: At the Heart of the Pregnancy: What Prenatal and Cardiovascular Genetic Counselors Need to Know about Maternal Heart Disease

Assessment of large copy number variants in patients with apparently isolated congenital left‐sided cardiac lesions reveals clinically relevant genomic events

Aktive Filter

Suchergebnisse filtern