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...

Presymptomatic and predictive genetic testing in minors: a systematic review of guidelines and position papers

Clinical genetics, 2006-11, Vol.70 (5), p.374-381

2006

Volltextzugriff (PDF)

Guiding Periodontal Pocket Recolonization: a Proof of Concept

Journal of dental research, 2007-11, Vol.86 (11), p.1078-1082

2007

Volltextzugriff (PDF)

Consensus on the use and interpretation of cystic fibrosis mutation analysis in clinical practice

Journal of cystic fibrosis, 2008-05, Vol.7 (3), p.179-196

2008

Volltextzugriff (PDF)

The Storage and Use of Biological Tissue Samples from Minors for Research: A Focus Group Study

Public health genomics, 2011-01, Vol.14 (2), p.68-76

2011

Volltextzugriff (PDF)

Bacteria Interfere with A. actinomycetemcomitans Colonization

Journal of dental research, 2007-07, Vol.86 (7), p.611-617

2007

Volltextzugriff (PDF)

The Ethical Introduction of Genome-Based Information and Technologies into Public Health

Public health genomics, 2013-01, Vol.16 (3), p.100-109

2013

Volltextzugriff (PDF)

Polyvariant mutant cystic fibrosis transmembrane conductance regulator genes. The polymorphic (Tg)m locus explains the partial penetrance of the T5 polymorphism as a disease mutation

The Journal of clinical investigation, 1998-01, Vol.101 (2), p.487-496

1998

Volltextzugriff (PDF)

Mutations in PMM2 , a phosphomannomutase gene on chromosome 16p13 in carbohydrate-deficient glycoprotein type I syndrome (Jaeken syndrome)

Nature genetics, 1997-05, Vol.16 (1), p.88-92

1997

Volltextzugriff (PDF)

Quadriceps and Grip Strength Are Related to Vitamin D Receptor Genotype in Elderly Nonobese Women

Journal of bone and mineral research, 1997-12, Vol.12 (12), p.2082-2088

1997

Volltextzugriff (PDF)

Predominance of beta-catenin mutations and beta-catenin dysregulation in sporadic aggressive fibromatosis (desmoid tumor)

Oncogene, 1999-11, Vol.18 (47), p.6615-6620

1999

Volltextzugriff (PDF)

Upregulation of Wilms’ tumour gene 1 ( WT1 ) in uterine sarcomas

European journal of cancer (1990), 2007-07, Vol.43 (10), p.1630-1637

2007

Volltextzugriff (PDF)

Towards quality assurance and harmonization of genetic testing services in the European Union

Nature biotechnology, 2004-10, Vol.22 (10), p.1230-1235

2004

Volltextzugriff (PDF)

Association of tumour necrosis factor alpha variants with the CF pulmonary phenotype

Thorax, 2005-04, Vol.60 (4), p.320-325

2005

Volltextzugriff (PDF)

Established cell lines used in cystic fibrosis research

Journal of cystic fibrosis, 2004-08, Vol.3, p.191-196

2004

Volltextzugriff (PDF)

Invasion and MMP expression profile in desmoid tumours

British journal of cancer, 2004-04, Vol.90 (7), p.1443-1449

2004

Volltextzugriff (PDF)

Marginal zone B-cell lymphomas of different sites share similar cytogenetic and morphologic features

Blood, 1996, Vol.87 (1), p.299-307

1996

Volltextzugriff (PDF)

Polymorphisms in the mannose binding lectin gene affect the cystic fibrosis pulmonary phenotype

Journal of medical genetics, 2004-08, Vol.41 (8), p.629-633

2004

Volltextzugriff (PDF)

Meer aandacht voor zeldzame ziekten in België

Tijdschrift voor geneeskunde, 2019 (6), p.368-372

2019

Volltextzugriff (PDF)

Lack of Homozygotes for the Most Frequent Disease Allele in Carbohydrate-Deficient Glycoprotein Syndrome Type 1A

American journal of human genetics, 1998-03, Vol.62 (3), p.542-550

1998

Volltextzugriff (PDF)

Genetic testing and quality control in diagnostic laboratories

Nature genetics, 2000-07, Vol.25 (3), p.259-260

2000

Volltextzugriff (PDF)

Cell surface heparan sulfate proteoglycans from human vascular endothelial cells. Core protein characterization and antithrombin III binding properties

The Journal of biological chemistry, 1992-10, Vol.267 (28), p.20435-20443

1992

Volltextzugriff (PDF)

Linkage and association of HLA class II genes with vitiligo in a Dutch population

British journal of dermatology (1951), 2001-07, Vol.145 (1), p.90-94

2001

Volltextzugriff (PDF)

Characteristic pattern of chromosomal gains and losses in marginal zone B cell lymphoma detected by comparative genomic hybridization

Leukemia, 1997-05, Vol.11 (5), p.747-758

1997

Volltextzugriff (PDF)

EuroGentest: Bericht zu den Fortschritten bei der Harmonisierung und Qualitätsverbesserung der europäischen Genetikeinrichtungen

Medizinische Genetik, 2008-03, Vol.20 (1), p.18-23

Cassiman, J.-J.

2008

Volltextzugriff (PDF)

Lack of association between estrogen receptor genotypes and bone mineral density, fracture history, or muscle strength in elderly women

Journal of bone and mineral research, 1999-09, Vol.14 (9), p.1576-1582

1999

Volltextzugriff (PDF)

1 – 25 von 696

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(603)
Mit Volltextzugriff
(555)

Publikationsform

1 weiteren anzeigen...

Weniger anzeigen...

Sprache

Erscheinungsjahr

n.n

Thema

Humans
(429)
Science & Technology
(396)
Life Sciences & Biomedicine
(389)
Biological And Medical Sciences
(241)
Male
(175)
Medical Sciences
(162)
Female
(154)
Genetics & Heredity
(150)
Adult
(97)
Fundamental And Applied Biological Sciences. Psychology
(94)
Middle Aged
(81)
Animals
(80)
Biochemistry & Molecular Biology
(74)
Base Sequence
(72)
Molecular Sequence Data
(71)
Cells, Cultured
(62)
Mutation
(56)
Polymerase Chain Reaction
(56)
Aged
(52)
Cell Biology
(52)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

Presymptomatic and predictive genetic testing in minors: a systematic review of guidelines and position papers

Guiding Periodontal Pocket Recolonization: a Proof of Concept

Consensus on the use and interpretation of cystic fibrosis mutation analysis in clinical practice

The Storage and Use of Biological Tissue Samples from Minors for Research: A Focus Group Study

Bacteria Interfere with A. actinomycetemcomitans Colonization

The Ethical Introduction of Genome-Based Information and Technologies into Public Health

Polyvariant mutant cystic fibrosis transmembrane conductance regulator genes. The polymorphic (Tg)m locus explains the partial penetrance of the T5 polymorphism as a disease mutation

Mutations in PMM2 , a phosphomannomutase gene on chromosome 16p13 in carbohydrate-deficient glycoprotein type I syndrome (Jaeken syndrome)

Quadriceps and Grip Strength Are Related to Vitamin D Receptor Genotype in Elderly Nonobese Women

Predominance of beta-catenin mutations and beta-catenin dysregulation in sporadic aggressive fibromatosis (desmoid tumor)

Upregulation of Wilms’ tumour gene 1 ( WT1 ) in uterine sarcomas

Towards quality assurance and harmonization of genetic testing services in the European Union

Association of tumour necrosis factor alpha variants with the CF pulmonary phenotype

Established cell lines used in cystic fibrosis research

Invasion and MMP expression profile in desmoid tumours

Marginal zone B-cell lymphomas of different sites share similar cytogenetic and morphologic features

Polymorphisms in the mannose binding lectin gene affect the cystic fibrosis pulmonary phenotype

Meer aandacht voor zeldzame ziekten in België

Lack of Homozygotes for the Most Frequent Disease Allele in Carbohydrate-Deficient Glycoprotein Syndrome Type 1A

Genetic testing and quality control in diagnostic laboratories

Cell surface heparan sulfate proteoglycans from human vascular endothelial cells. Core protein characterization and antithrombin III binding properties

Linkage and association of HLA class II genes with vitiligo in a Dutch population

Characteristic pattern of chromosomal gains and losses in marginal zone B cell lymphoma detected by comparative genomic hybridization

EuroGentest: Bericht zu den Fortschritten bei der Harmonisierung und Qualitätsverbesserung der europäischen Genetikeinrichtungen

Lack of association between estrogen receptor genotypes and bone mineral density, fracture history, or muscle strength in elderly women

Suchergebnisse filtern