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...

Germline ATM Mutations Detected by Somatic DNA Sequencing in Lethal Prostate Cancer

European urology open science (Online), 2023-06, Vol.52, p.72-78

2023

Volltextzugriff (PDF)

Non-invasive Technology Advances in Cancer—A Review of the Advances in the Liquid Biopsy for Endometrial and Ovarian Cancers

Frontiers in digital health, 2020-12, Vol.2, p.573010-573010

2020

Volltextzugriff (PDF)

Postgraduate training in Cancer Genetics—a cross-specialty survey exploring experience of clinicians in Ireland

Irish journal of medical science, 2022-06, Vol.191 (3), p.1427-1434

2022

Volltextzugriff (PDF)

Teaching Radiology to Medical Students—There Is a Need for Change to Better Prepare Students for Clinical Practice

Academic radiology, 2017-04, Vol.24 (4), p.506-513

2017

Volltextzugriff (PDF)

A systematic review and meta‐analysis of telephone vs in‐person genetic counseling in BRCA1/BRCA2 genetic testing

Journal of genetic counseling, 2021-04, Vol.30 (2), p.563-573

2021

Volltextzugriff (PDF)

Increasing Reporting of Adverse Events to Improve the Educational Value of the Morbidity and Mortality Conference

Journal of the American College of Surgeons, 2013, Vol.216 (1), p.50-56

2013

Volltextzugriff (PDF)

KIT-Associated Familial GIST Syndrome: Response to Tyrosine Kinase Inhibitors and Implications for Risk Management

The oncologist (Dayton, Ohio), 2022-08, Vol.27 (8), p.615-620

2022

Volltextzugriff (PDF)

Clinical use of the Oncotype DX genomic test to guide treatment decisions for patients with invasive breast cancer

Breast cancer targets and therapy, 2017-01, Vol.9, p.393-400

2017

Volltextzugriff (PDF)

Characterization of sebaceous and non-sebaceous cutaneous manifestations in patients with lynch syndrome: a systematic review

Familial cancer, 2023-04, Vol.22 (2), p.167-175

2023

Volltextzugriff (PDF)

Management of patients with germline predisposition to haematological malignancies considered for allogeneic blood and marrow transplantation: Best practice consensus guidelines from the UK Cancer Genetics Group (UKCGG), CanGene‐CanVar, NHS England Genomic Laboratory Hub (GLH) Haematological Malignancies Working Group and the British Society of Blood and Marrow Transplantation and cellular therapy (BSBMTCT)

British journal of haematology, 2023-04, Vol.201 (1), p.35-44

2023

Volltextzugriff (PDF)

Germline predisposition to haematological malignancies: Best practice consensus guidelines from the UK Cancer Genetics Group (UKCGG), CanGene‐CanVar and the NHS England Haematological Oncology Working Group

British journal of haematology, 2023-04, Vol.201 (1), p.25-34

2023

Volltextzugriff (PDF)

Embryonal Rhabdomyosarcoma of the Ovary and Fallopian Tube: Rare Neoplasms Associated With Germline and Somatic DICER1 Mutations

The American journal of surgical pathology, 2020-06, Vol.44 (6), p.738-747

2020

Volltextzugriff (PDF)

Differentiated Thyroid Cancer: How Do Current Practice Guidelines Affect Management?

European thyroid journal, 2018-11, Vol.7 (6), p.319-326

2018

Volltextzugriff (PDF)

A pilot of Blood-First diagnostic cell free DNA (cfDNA) next generation sequencing (NGS) in patients with suspected advanced lung cancer

Lung cancer (Amsterdam, Netherlands), 2022-03, Vol.165, p.34-42

2022

Volltextzugriff (PDF)

Sleep disordered breathing in children with Down syndrome in the Republic of Ireland

American journal of medical genetics. Part A, 2020-12, Vol.182 (12), p.2847-2856

2020

Volltextzugriff (PDF)

Using cancer phenotype sex-specificity to enable unbiased penetrance estimation of SMARCA4 pathogenic variants for small cell carcinoma of the ovary, hypercalcemic type (SCCOHT)

Genetics in medicine, 2024-10, p.101287, Article 101287

2024

Volltextzugriff (PDF)

Should All Individuals Be Screened for Genetic Predisposition to Cancer?

Genetics Research, 2021, Vol.2021, p.6611963-6

2021

Volltextzugriff (PDF)

A clinical, molecular genetics and pathological study of a FTDP-17 family with a heterozygous splicing variant c.823-10G>T at the intron 9/exon 10 of the MAPT gene

Neurobiology of aging, 2021-10, Vol.106, p.343.e1-343.e8

2021

Volltextzugriff (PDF)

Uterine leiomyomatosis in adolescents and young adults (AYAs) may represent a narrow phenotypic variant of FH tumour predisposition syndrome

Familial cancer, 2022-07, Vol.21 (3), p.357-362

2022

Volltextzugriff (PDF)

Fibroadenoma in vulval ectopic breast tissue in a patient with PTEN Hamartoma Tumour Syndrome

Familial cancer, 2022-07, Vol.21 (3), p.363-368

2022

Volltextzugriff (PDF)

Recommendations for laboratory workflow that better support centralised amalgamation of genomic variant data: findings from CanVIG-UK national molecular laboratory survey

Journal of medical genetics, 2024-03, Vol.61 (4), p.305-312

2024

Volltextzugriff (PDF)

Fumarate Metabolic Signature for the Detection of Reed Syndrome in Humans

Clinical cancer research, 2020-01, Vol.26 (2), p.391-396

2020

Volltextzugriff (PDF)

Diagnostic yield from cardiac gene testing for inherited cardiac conditions and re-evaluation of pre-ACMG variants of uncertain significance

Irish journal of medical science, 2024-08, Vol.193 (4), p.1775-1785

2024

Volltextzugriff (PDF)

1 – 25 von 54

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(51)
Mit Volltextzugriff
(47)

Publikationsform

Artikel
(53)
Berichte
(1)

Sprache

Englisch
(54)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(1)
... seit 90 Tagen
(2)

Menü

Weitere Dienste

Einstellungen

Germline ATM Mutations Detected by Somatic DNA Sequencing in Lethal Prostate Cancer

Non-invasive Technology Advances in Cancer—A Review of the Advances in the Liquid Biopsy for Endometrial and Ovarian Cancers

Postgraduate training in Cancer Genetics—a cross-specialty survey exploring experience of clinicians in Ireland

Teaching Radiology to Medical Students—There Is a Need for Change to Better Prepare Students for Clinical Practice

A systematic review and meta‐analysis of telephone vs in‐person genetic counseling in BRCA1/BRCA2 genetic testing

Increasing Reporting of Adverse Events to Improve the Educational Value of the Morbidity and Mortality Conference

KIT-Associated Familial GIST Syndrome: Response to Tyrosine Kinase Inhibitors and Implications for Risk Management

Clinical use of the Oncotype DX genomic test to guide treatment decisions for patients with invasive breast cancer

Characterization of sebaceous and non-sebaceous cutaneous manifestations in patients with lynch syndrome: a systematic review

Germline predisposition to haematological malignancies: Best practice consensus guidelines from the UK Cancer Genetics Group (UKCGG), CanGene‐CanVar and the NHS England Haematological Oncology Working Group

Embryonal Rhabdomyosarcoma of the Ovary and Fallopian Tube: Rare Neoplasms Associated With Germline and Somatic DICER1 Mutations

Differentiated Thyroid Cancer: How Do Current Practice Guidelines Affect Management?

A pilot of Blood-First diagnostic cell free DNA (cfDNA) next generation sequencing (NGS) in patients with suspected advanced lung cancer

Sleep disordered breathing in children with Down syndrome in the Republic of Ireland

Using cancer phenotype sex-specificity to enable unbiased penetrance estimation of SMARCA4 pathogenic variants for small cell carcinoma of the ovary, hypercalcemic type (SCCOHT)

Corrigendum to: A clinical, molecular genetics and pathological study of a FTDP-17 family with a heterozygous splicing variant c.823–10 G>T at the intron 9/exon 10 of the MAPT gene

Should All Individuals Be Screened for Genetic Predisposition to Cancer?

A clinical, molecular genetics and pathological study of a FTDP-17 family with a heterozygous splicing variant c.823-10G>T at the intron 9/exon 10 of the MAPT gene

Uterine leiomyomatosis in adolescents and young adults (AYAs) may represent a narrow phenotypic variant of FH tumour predisposition syndrome

Fibroadenoma in vulval ectopic breast tissue in a patient with PTEN Hamartoma Tumour Syndrome

Recommendations for laboratory workflow that better support centralised amalgamation of genomic variant data: findings from CanVIG-UK national molecular laboratory survey

UK recommendations for SDHA germline genetic testing and surveillance in clinical practice

Fumarate Metabolic Signature for the Detection of Reed Syndrome in Humans

Diagnostic yield from cardiac gene testing for inherited cardiac conditions and re-evaluation of pre-ACMG variants of uncertain significance

Suchergebnisse filtern