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...

Clinical and molecular features of 66 patients with musculocontractural Ehlers−Danlos syndrome caused by pathogenic variants in CHST14 (mcEDS-CHST14)

Journal of medical genetics, 2022-09, Vol.59 (9), p.865-877

2022

Volltextzugriff (PDF)

Hypermobile Ehlers-Danlos syndrome (hEDS) phenotype in fragile X premutation carriers: case series

Journal of medical genetics, 2022-07, Vol.59 (7), p.687-690

2022

Volltextzugriff (PDF)

Ehlers-Danlos syndrome has varied molecular mechanisms

Journal of medical genetics, 1997-05, Vol.34 (5), p.400-410

1997

Volltextzugriff (PDF)

Genetic complexity of diagnostically unresolved Ehlers-Danlos syndrome

Journal of medical genetics, 2024-03, Vol.61 (3), p.232-238

2024

Volltextzugriff (PDF)

Exome sequencing of 1190 non-syndromic clubfoot cases reveals HOXD12 as a novel disease gene

Journal of medical genetics, 2024-07, Vol.61 (7), p.699-706

2024

Volltextzugriff (PDF)

Arterial complications in classical Ehlers-Danlos syndrome: a case series

Journal of medical genetics, 2020-11, Vol.57 (11), p.769-776

2020

Volltextzugriff (PDF)

Long-read sequencing identifies an SVA_D retrotransposon insertion deep within the intron of ATP7A as a novel cause of occipital horn syndrome

Journal of medical genetics, 2024-10, Vol.61 (10), p.950-958

2024

Volltextzugriff (PDF)

Ehlers-Danlos syndrome and periventricular nodular heterotopia in a Spanish family with a single FLNA mutation

Journal of medical genetics, 2006-03, Vol.43 (3), p.232-237

2006

Volltextzugriff (PDF)

Pathogenic variants in PLOD3 result in a Stickler syndrome-like connective tissue disorder with vascular complications

Journal of medical genetics, 2019-09, Vol.56 (9), p.629-638

2019

Volltextzugriff (PDF)

A single base mutation in COL5A2 causes Ehlers-Danlos syndrome type II

Journal of medical genetics, 1998-10, Vol.35 (10), p.846-848

1998

Volltextzugriff (PDF)

An exon skipping mutation of a type V collagen gene (COL5A1) in Ehlers-Danlos syndrome

Journal of medical genetics, 1996-11, Vol.33 (11), p.940-946

1996

Volltextzugriff (PDF)

Detection and characterisation of an overmodified type III collagen by analysis of non-cutaneous connective tissues in a patient with Ehlers-Danlos syndrome IV

Journal of medical genetics, 1992-06, Vol.29 (6), p.375-380

1992

Volltextzugriff (PDF)

Homozygosity mapping of a gene for arterial tortuosity syndrome to chromosome 20q13

Journal of medical genetics, 2003-10, Vol.40 (10), p.747-751

2003

Volltextzugriff (PDF)

Testing for osteogenesis imperfecta in cases of suspected non-accidental injury

Journal of medical genetics, 2002-06, Vol.39 (6), p.382-386

2002

Volltextzugriff (PDF)

Total absence of the α2(I) chain of collagen type I causes a rare form of Ehlers-Danlos syndrome with hypermobility and propensity to cardiac valvular problems

Journal of medical genetics, 2006-07, Vol.43 (7), p.e36-e36

2006

Volltextzugriff (PDF)

Met>Val substitution in a highly conserved region of the pro-α1(I) collagen C-propeptide domain causes alternative splicing and a mild EDS/OI phenotype

Journal of medical genetics, 2004-07, Vol.41 (7), p.e96-e96

2004

Volltextzugriff (PDF)

Mapping of a de novo unequal crossover causing a deletion of the steroid 21-hydroxylase (CYP21A2) gene and a non-functional hybrid tenascin-X (TNXB) gene

Journal of medical genetics, 2003-05, Vol.40 (5), p.e53-53

2003

Volltextzugriff (PDF)

A T super(+6) to C super(+6) mutation in the donor splice site of COL3A1 IVS7 causes exon skipping and results in Ehlers-Danlos syndrome type IV

Journal of medical genetics, 1993-01, Vol.30 (5), p.376-380

1993

Volltextzugriff (PDF)

1 – 18 von 18

Suche als RSS-Feed

Aktive Filter

KollektionWiley Online Library

SpracheHebräisch

Zeitschrift / SerieJournal Of Medical Genetics

ThemaEhlers-Danlos Syndrome

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(18)
Mit Volltextzugriff
(11)

Publikationsform

Artikel
(18)

Sprache

Englisch
(18)

Erscheinungsjahr

n.n

Thema

14 weitere anzeigen...

Weniger anzeigen...

Kollektion

Electronic Journals Library
(18)
BMJ Publishing
(18)
Journals@Ovid Full Text
(17)
BMJ Journals Archiv - DFG Nationallizenzen
(17)
MEDLINE
(13)

Menü

Weitere Dienste

Einstellungen

Clinical and molecular features of 66 patients with musculocontractural Ehlers−Danlos syndrome caused by pathogenic variants in CHST14 (mcEDS-CHST14)

Hypermobile Ehlers-Danlos syndrome (hEDS) phenotype in fragile X premutation carriers: case series

Ehlers-Danlos syndrome has varied molecular mechanisms

Genetic complexity of diagnostically unresolved Ehlers-Danlos syndrome

Exome sequencing of 1190 non-syndromic clubfoot cases reveals HOXD12 as a novel disease gene

Arterial complications in classical Ehlers-Danlos syndrome: a case series

Long-read sequencing identifies an SVA_D retrotransposon insertion deep within the intron of ATP7A as a novel cause of occipital horn syndrome

Ehlers-Danlos syndrome and periventricular nodular heterotopia in a Spanish family with a single FLNA mutation

Pathogenic variants in PLOD3 result in a Stickler syndrome-like connective tissue disorder with vascular complications

A single base mutation in COL5A2 causes Ehlers-Danlos syndrome type II

An exon skipping mutation of a type V collagen gene (COL5A1) in Ehlers-Danlos syndrome

Detection and characterisation of an overmodified type III collagen by analysis of non-cutaneous connective tissues in a patient with Ehlers-Danlos syndrome IV

Homozygosity mapping of a gene for arterial tortuosity syndrome to chromosome 20q13

Testing for osteogenesis imperfecta in cases of suspected non-accidental injury

Total absence of the α2(I) chain of collagen type I causes a rare form of Ehlers-Danlos syndrome with hypermobility and propensity to cardiac valvular problems

Met>Val substitution in a highly conserved region of the pro-α1(I) collagen C-propeptide domain causes alternative splicing and a mild EDS/OI phenotype

Mapping of a de novo unequal crossover causing a deletion of the steroid 21-hydroxylase (CYP21A2) gene and a non-functional hybrid tenascin-X (TNXB) gene

A T super(+6) to C super(+6) mutation in the donor splice site of COL3A1 IVS7 causes exon skipping and results in Ehlers-Danlos syndrome type IV

Aktive Filter

Suchergebnisse filtern