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...

Hereditary paraganglioma targets diverse paraganglia

Journal of medical genetics, 2002-09, Vol.39 (9), p.617-622

Baysal, B E

2002

Volltextzugriff (PDF)

Clinical and molecular progress in hereditary paraganglioma

Journal of medical genetics, 2008-11, Vol.45 (11), p.689-694

Baysal, B E

2008

Volltextzugriff (PDF)

Prevalence of SDHB, SDHC, and SDHD germline mutations in clinic patients with head and neck paragangliomas

Journal of medical genetics, 2002-03, Vol.39 (3), p.178-183

2002

Volltextzugriff (PDF)

Mutations in SDHD, A Mitochondrial Complex II Gene, in Hereditary Paraganglioma

Science (American Association for the Advancement of Science), 2000-02, Vol.287 (5454), p.848-851

2000

Volltextzugriff (PDF)

An Alu-mediated partial SDHC deletion causes familial and sporadic paraganglioma

Journal of medical genetics, 2004-09, Vol.41 (9), p.703-709

2004

Volltextzugriff (PDF)

On the association of succinate dehydrogenase mutations with hereditary paraganglioma

Trends in endocrinology and metabolism, 2003-12, Vol.14 (10), p.453-459

Baysal, Bora E.

2003

Volltextzugriff (PDF)

Germ line insertion of mtDNA at the breakpoint junction of a reciprocal constitutional translocation

Human genetics, 2001-08, Vol.109 (2), p.216-223

2001

Volltextzugriff (PDF)

Altitude is a phenotypic modifier in hereditary paraganglioma type 1: evidence for an oxygen-sensing defect

Human genetics, 2003-08, Vol.113 (3), p.228-237

2003

Volltextzugriff (PDF)

Centrifugal enhancement of retroviral mediated gene transfer

Journal of virological methods, 1995-08, Vol.54 (2-3), p.131-143

1995

Volltextzugriff (PDF)

Fine mapping of an imprinted gene for familial nonchromaffin paragangliomas, on chromosome 11q23

American journal of human genetics, 1997, Vol.60 (1), p.121-132

1997

Volltextzugriff (PDF)

Fine Mapping of the Split-Hand/Split-Foot Locus ( SHFM3) at 10q24: Evidence for Anticipation and Segregation Distortion

American journal of human genetics, 1999-06, Vol.64 (6), p.1646-1654

1999

Volltextzugriff (PDF)

Etiopathogenesis and clinical presentation of carotid body tumors

Microscopy research and technique, 2002-11, Vol.59 (3), p.256-261

2002

Volltextzugriff (PDF)

Nearly all hereditary paragangliomas in The Netherlands are caused by two founder mutations in the SDHD gene

Genes chromosomes & cancer, 2001-07, Vol.31 (3), p.274-281

2001

Volltextzugriff (PDF)

Genetic Analysis in the Diagnosis of Familial Paragangliomas

The Laryngoscope, 2000, Vol.110 (7), p.1225-1229

2000

Volltextzugriff (PDF)

Phenotypic dichotomy in mitochondrial complex II genetic disorders

Journal of molecular medicine (Berlin, Germany), 2001-09, Vol.79 (9), p.495-503

2001

Volltextzugriff (PDF)

A High-Resolution STS, EST, and Gene-Based Physical Map of the Hereditary Paraganglioma Region on Chromosome 11q23

Genomics (San Diego, Calif.), 1997-09, Vol.44 (2), p.214-221

1997

Volltextzugriff (PDF)

Genetics of familial paragangliomas: past, present, and future

Otolaryngologic clinics of North America, 2001-10, Vol.34 (5), p.863-879

Baysal, B E

2001

Volltextzugriff (PDF)

Novel mutations in the SDHD gene in pedigrees with familial carotid body paraganglioma and sensorineural hearing loss

Genes chromosomes & cancer, 2001-07, Vol.31 (3), p.255-263

2001

Volltextzugriff (PDF)

Proportion of Heritable Paraganglioma Cases and Associated Clinical Characteristics

The Laryngoscope, 2001-10, Vol.111 (10), p.1822-1827

2001

Volltextzugriff (PDF)

Genomic structure of the human PLZF gene

Gene, 1999-08, Vol.236 (1), p.21-24

1999

Volltextzugriff (PDF)

Genotype and Tumor Locus Determine Expression Profile of Pseudohypoxic Pheochromocytomas and Paragangliomas

Neoplasia (New York, N.Y.), 2013-04, Vol.15 (4), p.435-IN22

2013

Volltextzugriff (PDF)

A high-resolution integrated map spanning the SDHD gene at 11q23: a 1.1-Mb BAC contig, a partial transcript map and 15 new repeat polymorphisms in a tumour-suppressor region

European journal of human genetics : EJHG, 2001-02, Vol.9 (2), p.121-129

2001

Volltextzugriff (PDF)

Predictors and prevalence of paraganglioma syndrome associated with mutations of the SDHC gene

JAMA : the journal of the American Medical Association, 2005-10, Vol.294 (16), p.2057

2005

Volltextzugriff (PDF)

Genomic imprinting and environment in hereditary paraganglioma

American journal of medical genetics. Part C, Seminars in medical genetics, 2004-08, Vol.129C (1), p.85-90

Baysal, Bora E.

2004

Volltextzugriff (PDF)

Bipolar affective disorder partially cosegregates with a balanced t(9;11)(p24;q23.1) chromosomal translocation in a small pedigree

American journal of medical genetics, 1998-02, Vol.81 (1), p.81-91

1998

Volltextzugriff (PDF)

1 – 25 von 151

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(140)
Mit Volltextzugriff
(128)

Publikationsform

Artikel
(148)
Tagungsberichte
(3)

Sprache

Englisch
(145)
Japanisch
(7)
Deutsch
(6)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Hereditary paraganglioma targets diverse paraganglia

Clinical and molecular progress in hereditary paraganglioma

Prevalence of SDHB, SDHC, and SDHD germline mutations in clinic patients with head and neck paragangliomas

Mutations in SDHD, A Mitochondrial Complex II Gene, in Hereditary Paraganglioma

An Alu-mediated partial SDHC deletion causes familial and sporadic paraganglioma

On the association of succinate dehydrogenase mutations with hereditary paraganglioma

Germ line insertion of mtDNA at the breakpoint junction of a reciprocal constitutional translocation

Altitude is a phenotypic modifier in hereditary paraganglioma type 1: evidence for an oxygen-sensing defect

Centrifugal enhancement of retroviral mediated gene transfer

Fine mapping of an imprinted gene for familial nonchromaffin paragangliomas, on chromosome 11q23

Fine Mapping of the Split-Hand/Split-Foot Locus ( SHFM3) at 10q24: Evidence for Anticipation and Segregation Distortion

Etiopathogenesis and clinical presentation of carotid body tumors

Nearly all hereditary paragangliomas in The Netherlands are caused by two founder mutations in the SDHD gene

Genetic Analysis in the Diagnosis of Familial Paragangliomas

Phenotypic dichotomy in mitochondrial complex II genetic disorders

A High-Resolution STS, EST, and Gene-Based Physical Map of the Hereditary Paraganglioma Region on Chromosome 11q23

Genetics of familial paragangliomas: past, present, and future

Novel mutations in the SDHD gene in pedigrees with familial carotid body paraganglioma and sensorineural hearing loss

Proportion of Heritable Paraganglioma Cases and Associated Clinical Characteristics

Genomic structure of the human PLZF gene

Genotype and Tumor Locus Determine Expression Profile of Pseudohypoxic Pheochromocytomas and Paragangliomas

A high-resolution integrated map spanning the SDHD gene at 11q23: a 1.1-Mb BAC contig, a partial transcript map and 15 new repeat polymorphisms in a tumour-suppressor region

Predictors and prevalence of paraganglioma syndrome associated with mutations of the SDHC gene

Genomic imprinting and environment in hereditary paraganglioma

Bipolar affective disorder partially cosegregates with a balanced t(9;11)(p24;q23.1) chromosomal translocation in a small pedigree

Suchergebnisse filtern