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...

The previously reported LRP4 c.4940C>T variant is not associated with syndactyly in cattle

Animal genetics, 2021-06, Vol.52 (3), p.380-381

2021

Volltextzugriff (PDF)

Using induced pluripotent stem cells to investigate cardiac phenotypes in Timothy syndrome

Nature (London), 2011-03, Vol.471 (7337), p.230-234

2011

Volltextzugriff (PDF)

Complications in the 2-Year Postoperative Period Following Pediatric Syndactyly Release

The Journal of hand surgery (American ed.), 2024-09, Vol.49 (9), p.927.e1-927.e6

2024

Volltextzugriff (PDF)

Long-term follow-up of a patient with type 2 Timothy syndrome and the partial efficacy of mexiletine

Gene, 2021-04, Vol.777, p.145465, Article 145465

2021

Volltextzugriff (PDF)

Assembly of functionally integrated human forebrain spheroids

Nature (London), 2017-05, Vol.545 (7652), p.54-59

2017

Volltextzugriff (PDF)

Revision Surgery Following Primary Reconstruction for Hand Syndactyly

The Journal of hand surgery (American ed.), 2024-10

2024

Volltextzugriff (PDF)

Like Father, Like Daughter - Ectodermal Dysplasia-Syndactyly Syndrome: A Case Report

The journal of hand surgery Asian-Pacific volume, 2024-06, Vol.29 (3), p.248-251

2024

Volltextzugriff (PDF)

Nonframeshifting indel variations in polyalanine repeat of HOXD13 gene underlies hereditary limb malformation for two Chinese families

Developmental dynamics, 2021-09, Vol.250 (9), p.1220-1228

2021

Volltextzugriff (PDF)

Sclerostin deficiency in humans

Bone (New York, N.Y.), 2017-03, Vol.96, p.51-62

2017

Volltextzugriff (PDF)

Evaluation of hexagonal flap for Syndactyly repair

Zanco journal of medical sciences, 2024-09, Vol.28 (2), p.235-247

2024

Volltextzugriff (PDF)

Sclerosteosis: Report of type 1 or 2 in three Indian Tamil families and literature review

Bone (New York, N.Y.), 2018-11, Vol.116, p.321-332

2018

Volltextzugriff (PDF)

Syndactyly repair in Kindler syndrome

Journal of dermatology, 2022-02, Vol.49 (2), p.e65-e66

2022

Volltextzugriff (PDF)

The Lrp4R1170Q Homozygous Knock‐In Mouse Recapitulates the Bone Phenotype of Sclerosteosis in Humans

Journal of bone and mineral research, 2017-08, Vol.32 (8), p.1739-1749

2017

Volltextzugriff (PDF)

A novel homozygous missense variant in LRP4 causing Cenani‐Lenz syndactyly syndrome and literature review

Molecular genetics & genomic medicine, 2024-01, Vol.12 (1), p.e2319-n/a

2024

Volltextzugriff (PDF)

Syndactyly: phenotypes, genetics and current classification

European journal of human genetics : EJHG, 2012-08, Vol.20 (8), p.817-824

Malik, Sajid

2012

Volltextzugriff (PDF)

Syndactyly release with the use of the Pelnac™ artificial dermal substitute without skin grafting

Journal of plastic, reconstructive & aesthetic surgery, 2023-09, Vol.84, p.115-120

2023

Volltextzugriff (PDF)

Refinement of Surgery for Postaxial Polysyndactyly of the Toes: Esthetic Outcome in Japanese Feet

Annals of plastic surgery, 2024-06

2024

Volltextzugriff (PDF)

Syndromic and non-syndromic disease-linked Cx43 mutations

FEBS letters, 2014-04, Vol.588 (8), p.1339-1348

Laird, Dale W.

2014

Volltextzugriff (PDF)

Truncating mutations of HIBCH tend to cause severe phenotypes in cases with HIBCH deficiency: a case report and brief literature review

Journal of human genetics, 2018-07, Vol.63 (7), p.851-855

2018

Volltextzugriff (PDF)

Oculodentodigital Dysplasia: A Cause of Hypomyelinating Leukodystrophy in Adults

Neurology, 2022-04, Vol.98 (16), p.675-677

2022

Volltextzugriff (PDF)

Novel long QT syndrome-associated missense mutation, L762F, in CACNA1C -encoded L-type calcium channel imparts a slower inactivation tau and increased sustained and window current

International journal of cardiology, 2016-10, Vol.220, p.290-298

2016

Volltextzugriff (PDF)

Webplasty using an external fixator for complex syndactyly caused by Apert syndrome

Journal of orthopaedic science : official journal of the Japanese Orthopaedic Association, 2024-05

2024

Volltextzugriff (PDF)

Case of generalized anhidrosis associated with diffuse reticular hyperpigmentation and syndactyly

Journal of dermatology, 2019-05, Vol.46 (5), p.e154-e155

2019

Volltextzugriff (PDF)

Identification of novel missense mutations associated with non-syndromic syndactyly in two vietnamese trios by whole exome sequencing

Clinica chimica acta, 2020-07, Vol.506, p.16-21

2020

Volltextzugriff (PDF)

A novel variant in AFF3 underlying isolated syndactyly

Clinical genetics, 2023-03, Vol.103 (3), p.341-345

2023

Volltextzugriff (PDF)

1 – 25 von 3.131

Suche als RSS-Feed

Aktive Filter

SprachePortugiesisch

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(2.265)
Mit Volltextzugriff
(2.060)

Publikationsform

3 weitere anzeigen...

Weniger anzeigen...

Sprache

15 weitere anzeigen...

Weniger anzeigen...

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Kollektion

MEDLINE
(2.694)
Ingenta Connect
(1.181)
Journals@Ovid
(1.087)
EZB-FREE-00999 freely available EZB journals
(916)
Wiley Online Library - AutoHoldings Journals
(606)
Wiley Online Library Full Collection 2018
(558)
IngentaConnect Journals
(503)
Elsevier ScienceDirect Journals Complete
(446)
Single Journals
(442)
EZB-NALI5-00465 Elsevier Archive NL
(255)
SpringerLink Journals - AutoHoldings
(244)
EZB-NALI2-00462 Springer Archive NL
(178)
Access via SAGE
(117)
BMJ Journals
(96)
Nature
(95)
Thieme Connect Journals
(88)
BMJ Journals Archiv - DFG Nationallizenzen
(82)
Access via Taylor & Francis
(53)
Access via Oxford University Press
(52)
Taylor & Francis Current Content Access
(50)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 7 Tagen
(1)
... seit 90 Tagen
(5)

Menü

Weitere Dienste

Einstellungen

The previously reported LRP4 c.4940C>T variant is not associated with syndactyly in cattle

Using induced pluripotent stem cells to investigate cardiac phenotypes in Timothy syndrome

Complications in the 2-Year Postoperative Period Following Pediatric Syndactyly Release

Long-term follow-up of a patient with type 2 Timothy syndrome and the partial efficacy of mexiletine

Assembly of functionally integrated human forebrain spheroids

Revision Surgery Following Primary Reconstruction for Hand Syndactyly

Like Father, Like Daughter - Ectodermal Dysplasia-Syndactyly Syndrome: A Case Report

Nonframeshifting indel variations in polyalanine repeat of HOXD13 gene underlies hereditary limb malformation for two Chinese families

Sclerostin deficiency in humans

Evaluation of hexagonal flap for Syndactyly repair

Sclerosteosis: Report of type 1 or 2 in three Indian Tamil families and literature review

Syndactyly repair in Kindler syndrome

The Lrp4R1170Q Homozygous Knock‐In Mouse Recapitulates the Bone Phenotype of Sclerosteosis in Humans

A novel homozygous missense variant in LRP4 causing Cenani‐Lenz syndactyly syndrome and literature review

Syndactyly: phenotypes, genetics and current classification

Syndactyly release with the use of the Pelnac™ artificial dermal substitute without skin grafting

Refinement of Surgery for Postaxial Polysyndactyly of the Toes: Esthetic Outcome in Japanese Feet

Syndromic and non-syndromic disease-linked Cx43 mutations

Truncating mutations of HIBCH tend to cause severe phenotypes in cases with HIBCH deficiency: a case report and brief literature review

Oculodentodigital Dysplasia: A Cause of Hypomyelinating Leukodystrophy in Adults

Novel long QT syndrome-associated missense mutation, L762F, in CACNA1C -encoded L-type calcium channel imparts a slower inactivation tau and increased sustained and window current

Webplasty using an external fixator for complex syndactyly caused by Apert syndrome

Case of generalized anhidrosis associated with diffuse reticular hyperpigmentation and syndactyly

Identification of novel missense mutations associated with non-syndromic syndactyly in two vietnamese trios by whole exome sequencing

A novel variant in AFF3 underlying isolated syndactyly

Aktive Filter

Suchergebnisse filtern