UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Sie befinden Sich nicht im Netzwerk der Universität Paderborn. Der Zugriff auf elektronische Ressourcen ist gegebenenfalls nur via VPN oder Shibboleth (DFN-AAI) möglich. mehr Informationen...

Beckwith–Wiedemann syndrome

International journal of oral and maxillofacial surgery, 2019-12, Vol.48 (12), p.1606-1607

Schendel, S.A.

2019

Link zum Volltext

Verfügbarkeit prüfen

Growth retardation versus overgrowth: Silver-Russell syndrome is genetically opposite to Beckwith-Wiedemann syndrome

Trends in genetics, 2008-04, Vol.24 (4), p.195-204

2008

Link zum Volltext

Verfügbarkeit prüfen

Surgical treatment of macroglossia in patients with Beckwith–Wiedemann syndrome: a 20-year experience and review of the literature

International journal of oral and maxillofacial surgery, 2012-03, Vol.41 (3), p.300-308

2012

Link zum Volltext

Verfügbarkeit prüfen

Cancer Risk in Beckwith-Wiedemann Syndrome: A Systematic Review and Meta-Analysis Outlining a Novel (Epi)Genotype Specific Histotype Targeted Screening Protocol

The Journal of pediatrics, 2016-09, Vol.176, p.142-149.e1

2016

Link zum Volltext

Verfügbarkeit prüfen

Recommendations of the Scientific Committee of the Italian Beckwith–Wiedemann Syndrome Association on the diagnosis, management and follow-up of the syndrome

European journal of medical genetics, 2016-01, Vol.59 (1), p.52-64

2016

Link zum Volltext

Verfügbarkeit prüfen

Tongue reduction in Beckwith–Wiedemann syndrome: outcome and treatment algorithm

International journal of oral and maxillofacial surgery, 2019-01, Vol.48 (1), p.9-16

2019

Link zum Volltext

Verfügbarkeit prüfen

CDKN1C Mutations in HELLP/Preeclamptic Mothers of Beckwith–Wiedemann Syndrome (BWS) Patients

Placenta (Eastbourne), 2009-06, Vol.30 (6), p.551-554

2009

Link zum Volltext

Verfügbarkeit prüfen

Beckwith-Wiedemann Syndrome and IVF: A Case-Control Study

American journal of human genetics, 2004-09, Vol.75 (3), p.526-528

2004

Link zum Volltext

Verfügbarkeit prüfen

Prenatal diagnosis of paternal duplication of 11p15.5→14.3: Its implication of Beckwith–Wiedemann syndrome

Taiwanese journal of obstetrics & gynecology, 2016-12, Vol.55 (6), p.877-880

2016

Link zum Volltext

Verfügbarkeit prüfen

Associations between the timing of tongue reduction surgery, (Epi)genotype, and dentoskeletal development in patients with Beckwith-Wiedemann syndrome

Journal of cranio-maxillo-facial surgery, 2023-09, Vol.51 (9), p.568-573

2023

Link zum Volltext

Verfügbarkeit prüfen

Association of In Vitro Fertilization with Beckwith-Wiedemann Syndrome and Epigenetic Alterations of LIT1 and H19

American journal of human genetics, 2003-01, Vol.72 (1), p.156-160

2003

Link zum Volltext

Verfügbarkeit prüfen

Oct motif variants in Beckwith–Wiedemann syndrome patients disrupt maintenance of the hypomethylated state of the H19/IGF2 imprinting control region

FEBS letters, 2020-05, Vol.594 (10), p.1517-1531

2020

Link zum Volltext

Verfügbarkeit prüfen

Pancreatic surgery in infants with Beckwith–Wiedemann Syndrome and Hyperinsulinism

Journal of pediatric surgery, 2013-12, Vol.48 (12), p.2511-2516

2013

Link zum Volltext

Verfügbarkeit prüfen

Imprinting in clusters: lessons from Beckwith-Wiedemann syndrome

Trends in Genetics, 1997-08, Vol.13 (8), p.330-334

1997

Link zum Volltext

Verfügbarkeit prüfen

In Vitro Fertilization May Increase the Risk of Beckwith-Wiedemann Syndrome Related to the Abnormal Imprinting of the KCNQ1OT Gene

American journal of human genetics, 2003-05, Vol.72 (5), p.1338-1341

2003

Link zum Volltext

Verfügbarkeit prüfen

Epigenotype, genotype, and phenotype analysis of patients in Taiwan with Beckwith–Wiedemann syndrome

Molecular genetics and metabolism, 2016-09, Vol.119 (1-2), p.8-13

2016

Link zum Volltext

Verfügbarkeit prüfen

Prenatal diagnosis of hypomethylation at KvDMR1 and Beckwith–Wiedemann syndrome in a pregnancy conceived by intracytoplasmic sperm injection and in vitro fertilization and embryo transfer

Taiwanese journal of obstetrics & gynecology, 2014-03, Vol.53 (1), p.90-94

2014

Link zum Volltext

Verfügbarkeit prüfen

Association between Beckwith-Wiedemann syndrome and assisted reproductive technology: A case series of 19 patients

Fertility and sterility, 2005-02, Vol.83 (2), p.349-354

2005

Link zum Volltext

Verfügbarkeit prüfen

CDKN1C mutations: two sides of the same coin

Trends in molecular medicine, 2014-11, Vol.20 (11), p.614-622

2014

Link zum Volltext

Verfügbarkeit prüfen

Long-term longitudinal evalutation of mandibular growth in patients with Beckwith-Wiedemann Syndrome treated and not treated with glossectomy

Journal of cranio-maxillo-facial surgery, 2020-12, Vol.48 (12), p.1126-1131

2020

Link zum Volltext

Verfügbarkeit prüfen

Taste and speech following surgical tongue reduction in children with Beckwith-Wiedemann syndrome

Journal of cranio-maxillo-facial surgery, 2016-06, Vol.44 (6), p.659-663

2016

Link zum Volltext

Verfügbarkeit prüfen

SNP arrays in Beckwith–Wiedemann syndrome: An improved diagnostic strategy

European journal of medical genetics, 2013-10, Vol.56 (10), p.546-550

2013

Link zum Volltext

Verfügbarkeit prüfen

The Clinical Course of an Overgrowth Syndrome, From Diagnosis in Infancy Through Adulthood: The Case of Beckwith–Wiedemann Syndrome

Current problems in pediatric and adolescent health care, 2015-04, Vol.45 (4), p.112-117

Pappas, John G., MD

2015

Link zum Volltext

Verfügbarkeit prüfen

First report of a successful pregnancy by preimplantation genetic testing for Beckwith-Wiedemann syndrome

Taiwanese journal of obstetrics & gynecology, 2022-01, Vol.61 (1), p.174-179

2022

Link zum Volltext

Verfügbarkeit prüfen

Beckwith Wiedemann syndrome: A population-based study on prevalence, prenatal diagnosis, associated anomalies and survival in Europe

European journal of medical genetics, 2018-09, Vol.61 (9), p.499-507

2018

Link zum Volltext

Verfügbarkeit prüfen

1 – 25 von 1.344

Suche als RSS-Feed

Aktive Filter

KollektionScienceDirect Journals (5 years ago - present)

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(1.290)
Mit Volltextzugriff
(1.195)

Publikationsform

Sprache

1 weiteren anzeigen...

Weniger anzeigen...

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

Fertility And Sterility
(84)
Journal Of Pediatric Surgery
(69)
The Journal Of Pediatrics
(45)
European Journal Of Medical Genetics
(43)
American Journal Of Human Genetics
(37)
Genomics
(36)
Placenta
(36)
The Lancet
(36)
Reproductive Biomedicine Online
(28)
Cancer Genetics And Cytogenetics
(23)

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(2)

Menü

Weitere Dienste

Einstellungen

Beckwith–Wiedemann syndrome

Growth retardation versus overgrowth: Silver-Russell syndrome is genetically opposite to Beckwith-Wiedemann syndrome

Surgical treatment of macroglossia in patients with Beckwith–Wiedemann syndrome: a 20-year experience and review of the literature

Cancer Risk in Beckwith-Wiedemann Syndrome: A Systematic Review and Meta-Analysis Outlining a Novel (Epi)Genotype Specific Histotype Targeted Screening Protocol

Recommendations of the Scientific Committee of the Italian Beckwith–Wiedemann Syndrome Association on the diagnosis, management and follow-up of the syndrome

Tongue reduction in Beckwith–Wiedemann syndrome: outcome and treatment algorithm

CDKN1C Mutations in HELLP/Preeclamptic Mothers of Beckwith–Wiedemann Syndrome (BWS) Patients

Beckwith-Wiedemann Syndrome and IVF: A Case-Control Study

Prenatal diagnosis of paternal duplication of 11p15.5→14.3: Its implication of Beckwith–Wiedemann syndrome

Associations between the timing of tongue reduction surgery, (Epi)genotype, and dentoskeletal development in patients with Beckwith-Wiedemann syndrome

Association of In Vitro Fertilization with Beckwith-Wiedemann Syndrome and Epigenetic Alterations of LIT1 and H19

Oct motif variants in Beckwith–Wiedemann syndrome patients disrupt maintenance of the hypomethylated state of the H19/IGF2 imprinting control region

Pancreatic surgery in infants with Beckwith–Wiedemann Syndrome and Hyperinsulinism

Imprinting in clusters: lessons from Beckwith-Wiedemann syndrome

In Vitro Fertilization May Increase the Risk of Beckwith-Wiedemann Syndrome Related to the Abnormal Imprinting of the KCNQ1OT Gene

Epigenotype, genotype, and phenotype analysis of patients in Taiwan with Beckwith–Wiedemann syndrome

Prenatal diagnosis of hypomethylation at KvDMR1 and Beckwith–Wiedemann syndrome in a pregnancy conceived by intracytoplasmic sperm injection and in vitro fertilization and embryo transfer

Association between Beckwith-Wiedemann syndrome and assisted reproductive technology: A case series of 19 patients

CDKN1C mutations: two sides of the same coin

Long-term longitudinal evalutation of mandibular growth in patients with Beckwith-Wiedemann Syndrome treated and not treated with glossectomy

Taste and speech following surgical tongue reduction in children with Beckwith-Wiedemann syndrome

SNP arrays in Beckwith–Wiedemann syndrome: An improved diagnostic strategy

The Clinical Course of an Overgrowth Syndrome, From Diagnosis in Infancy Through Adulthood: The Case of Beckwith–Wiedemann Syndrome

First report of a successful pregnancy by preimplantation genetic testing for Beckwith-Wiedemann syndrome

Beckwith Wiedemann syndrome: A population-based study on prevalence, prenatal diagnosis, associated anomalies and survival in Europe

Aktive Filter

Suchergebnisse filtern