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...

"I want to know what's in Pandora's box": Comparing stakeholder perspectives on incidental findings in clinical whole genomic sequencing

American journal of medical genetics. Part A, 2012-10, Vol.158A (10), p.2519-2525

2012

Volltextzugriff (PDF)

Costs of caring for children with an intellectual developmental disorder

Disability and health journal, 2015-10, Vol.8 (4), p.646-651

2015

Volltextzugriff (PDF)

Paternalism and the ACMG recommendations on genomic incidental findings: patients seen but not heard

Genetics in medicine, 2013-09, Vol.15 (9), p.751-752

2013

Volltextzugriff (PDF)

Indigenous Peoples and genomics: Starting a conversation

Journal of genetic counseling, 2019-04, Vol.28 (2), p.407-418

2019

Volltextzugriff (PDF)

A novel online genomic counseling and variant interpretation certificate: Learning design, learning analytics, and evaluation

Journal of genetic counseling, 2023-12, Vol.32 (6), p.1280-1287

2023

Volltextzugriff (PDF)

Comparing the ability of OPTION12 and OPTION5 to assess shared decision-making in genetic counselling

Patient education and counseling, 2016-10, Vol.99 (10), p.1717-1723

2016

Volltextzugriff (PDF)

Assessing an Interactive Online Tool to Support Parents' Genomic Testing Decisions

Journal of genetic counseling, 2019-02, Vol.28 (1), p.10-17

2019

Volltextzugriff (PDF)

Parents' Perspectives on Supporting Their Decision Making in Genome-Wide Sequencing

Journal of nursing scholarship, 2016-05, Vol.48 (3), p.265-275

2016

Volltextzugriff (PDF)

Comparing the ability of OPTION(12) and OPTION(5) to assess shared decision-making in genetic counselling

Patient education and counseling, 2016-10, Vol.99 (10), p.1717-1723

2016

Volltextzugriff (PDF)

Assessing Shared Decision‐Making Clinical Behaviors Among Genetic Counsellors

Journal of genetic counseling, 2019-02, Vol.28 (1), p.40-49

2019

Volltextzugriff (PDF)

Parental perceived value of a diagnosis for intellectual disability (ID): A qualitative comparison of families with and without a diagnosis for their child's ID

American journal of medical genetics. Part A, 2009-11, Vol.149A (11), p.2393-2402

2009

Volltextzugriff (PDF)

Cardiovascular malformations and other cardiovascular abnormalities in neurofibromatosis 1

American journal of medical genetics, 2000-11, Vol.95 (2), p.108-117

2000

Volltextzugriff (PDF)

Type 1 neurofibromatosis: A descriptive analysis of the disorder in 1,728 patients

American journal of medical genetics, 1997-05, Vol.70 (2), p.138-143

1997

Volltextzugriff (PDF)

Linkage analysis of X-linked cleft palate and ankyloglossia in Manitoba Mennonite and British Columbia Native kindreds

Human genetics, 1994-08, Vol.94 (2), p.141-148

1994

Volltextzugriff (PDF)

Descriptive analysis of tibial pseudarthrosis in patients with neurofibromatosis 1

American journal of medical genetics, 1999-06, Vol.84 (5), p.413-419

1999

Volltextzugriff (PDF)

Chromosome 3 anomalies investigated by genome wide SNP analysis of benign, low malignant potential and low grade ovarian serous tumours

PloS one, 2011-12, Vol.6 (12), p.e28250-e28250

2011

Volltextzugriff (PDF)

Effectiveness of Covid-19 Vaccines in Ambulatory and Inpatient Care Settings

The New England journal of medicine, 2021-10, Vol.385 (15), p.1355-1371

2021

Volltextzugriff (PDF)

Growth-Friendly Spine Surgery in Arthrogryposis Multiplex Congenita

Journal of bone and joint surgery. American volume, 2021-04, Vol.103 (8), p.715-726

2021

Volltextzugriff (PDF)

The genomic landscape of TP53 and p53 annotated high grade ovarian serous carcinomas from a defined founder population associated with patient outcome

PloS one, 2012-09, Vol.7 (9), p.e45484-e45484

2012

Volltextzugriff (PDF)

The stepwise process of integrating a genetic counsellor into primary care

European journal of human genetics : EJHG, 2022-07, Vol.30 (7), p.772-781

2022

Volltextzugriff (PDF)

Glaucoma-Related Adverse Events in the First 5 Years After Unilateral Cataract Removal in the Infant Aphakia Treatment Study

JAMA ophthalmology, 2015-08, Vol.133 (8), p.907

2015

Volltextzugriff (PDF)

Low- and Very Low-Dose Bevacizumab for Retinopathy of Prematurity: Reactivations, Additional Treatments, and 12-Month Outcomes

Ophthalmology (Rochester, Minn.), 2022-10, Vol.129 (10), p.1120-1128

2022

Volltextzugriff (PDF)

A Novel Small-Molecule Inhibitor of MRCK Prevents Radiation-Driven Invasion in Glioblastoma

Cancer research (Chicago, Ill.), 2018-11, Vol.78 (22), p.6509-6522

2018

Volltextzugriff (PDF)

Genetic counselors outside of the genetics clinic: Roles, practices, and ethico-legal implications in light of lagging legal recognition across Canada

Journal of genetic counseling, 2024-07

2024

Volltextzugriff (PDF)

Low-Dose 0.01% Atropine Eye Drops vs Placebo for Myopia Control: A Randomized Clinical Trial

JAMA ophthalmology, 2023-08, Vol.141 (8), p.756

2023

Volltextzugriff (PDF)

1 – 25 von 73

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(51)
Mit Volltextzugriff
(66)

Publikationsform

Sprache

Englisch
(73)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

"I want to know what's in Pandora's box": Comparing stakeholder perspectives on incidental findings in clinical whole genomic sequencing

Costs of caring for children with an intellectual developmental disorder

Paternalism and the ACMG recommendations on genomic incidental findings: patients seen but not heard

Indigenous Peoples and genomics: Starting a conversation

A novel online genomic counseling and variant interpretation certificate: Learning design, learning analytics, and evaluation

Comparing the ability of OPTION12 and OPTION5 to assess shared decision-making in genetic counselling

Assessing an Interactive Online Tool to Support Parents' Genomic Testing Decisions

Parents' Perspectives on Supporting Their Decision Making in Genome-Wide Sequencing

Comparing the ability of OPTION(12) and OPTION(5) to assess shared decision-making in genetic counselling

Assessing Shared Decision‐Making Clinical Behaviors Among Genetic Counsellors

Parental perceived value of a diagnosis for intellectual disability (ID): A qualitative comparison of families with and without a diagnosis for their child's ID

Cardiovascular malformations and other cardiovascular abnormalities in neurofibromatosis 1

Type 1 neurofibromatosis: A descriptive analysis of the disorder in 1,728 patients

Linkage analysis of X-linked cleft palate and ankyloglossia in Manitoba Mennonite and British Columbia Native kindreds

Descriptive analysis of tibial pseudarthrosis in patients with neurofibromatosis 1

Chromosome 3 anomalies investigated by genome wide SNP analysis of benign, low malignant potential and low grade ovarian serous tumours

Effectiveness of Covid-19 Vaccines in Ambulatory and Inpatient Care Settings

Growth-Friendly Spine Surgery in Arthrogryposis Multiplex Congenita

The genomic landscape of TP53 and p53 annotated high grade ovarian serous carcinomas from a defined founder population associated with patient outcome

The stepwise process of integrating a genetic counsellor into primary care

Glaucoma-Related Adverse Events in the First 5 Years After Unilateral Cataract Removal in the Infant Aphakia Treatment Study

Low- and Very Low-Dose Bevacizumab for Retinopathy of Prematurity: Reactivations, Additional Treatments, and 12-Month Outcomes

A Novel Small-Molecule Inhibitor of MRCK Prevents Radiation-Driven Invasion in Glioblastoma

Genetic counselors outside of the genetics clinic: Roles, practices, and ethico-legal implications in light of lagging legal recognition across Canada

Low-Dose 0.01% Atropine Eye Drops vs Placebo for Myopia Control: A Randomized Clinical Trial

Suchergebnisse filtern