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...

Novel homo- and hemizygous mutations in EZH2 in myeloid malignancies

Leukemia, 2010-10, Vol.24 (10), p.1799-1804

2010

Volltextzugriff (PDF)

Evidence for linkage on 21q and 7q in a subset of autism characterized by developmental regression

Molecular psychiatry, 2005-08, Vol.10 (8), p.741-746

2005

Volltextzugriff (PDF)

Genotype-phenotype correlations in Rubinstein-Taybi syndrome

American journal of medical genetics. Part A, 2008-10, Vol.146A (19), p.2512-2519

2008

Volltextzugriff (PDF)

Linkage analysis for autism in a subset families with obsessive-compulsive behaviors: Evidence for an autism susceptibility gene on chromosome 1 and further support for susceptibility genes on chromosome 6 and 19

Molecular psychiatry, 2004-02, Vol.9 (2), p.144-150

2004

Volltextzugriff (PDF)

Identification of novel coding mutation in C1qA gene in an African–American pedigree with lupus and C1q deficiency

Lupus, 2012-09, Vol.21 (10), p.1113-1118

2012

Volltextzugriff (PDF)

OP0212 Analysis of the immunochip in a large cohort of oligo- and polyarthritis juvenile idiopathic arthritis (JIA) cases confirms previous and identifies novel associations

Annals of the rheumatic diseases, 2013-06, Vol.71 (Suppl 3), p.127-127

2013

Volltextzugriff (PDF)

Genome scan of idiopathic generalized epilepsy: Evidence for major susceptibility gene and modifying genes influencing the seizure type

Annals of neurology, 2001-03, Vol.49 (3), p.328-335

2001

Volltextzugriff (PDF)

Ethosuximide, valproic acid, and lamotrigine in childhood absence epilepsy: Initial monotherapy outcomes at 12 months

Epilepsia (Copenhagen), 2013-01, Vol.54 (1), p.141-155

2013

Volltextzugriff (PDF)

Response by Dr Molloy

Molecular psychiatry, 2006-07, Vol.11 (7), p.619-619

2006

Volltextzugriff (PDF)

Ethosuximide, Valproic Acid, and Lamotrigine in Childhood Absence Epilepsy

The New England journal of medicine, 2010-03, Vol.362 (9), p.790-799

2010

Volltextzugriff (PDF)

Gaucher's disease: identification of novel mutant alleles and genotype-phenotype relationships

Clinical genetics, 2003-07, Vol.64 (1), p.57-64

2003

Volltextzugriff (PDF)

Evidence for linkage on 21q and 7q in a subset of autism characterized by developmental regression

Molecular psychiatry, 2005-08, Vol.10 (8), p.741-746

2005

Volltextzugriff (PDF)

Characterization of neuronopathic Gaucher disease among ethnic Poles

Genetics in medicine, 2006-01, Vol.8 (1), p.8-16

2006

Volltextzugriff (PDF)

Fucosyltransferase 2 Non-Secretor and Low Secretor Status Predicts Severe Outcomes in Premature Infants

The Journal of pediatrics, 2011-05, Vol.158 (5), p.745-751

2011

Volltextzugriff (PDF)

Genotoxicity and Integration Pattern of Foamy Virus Vectors with Strong Internal Viral Enhancers in In Vitro Immortalized Mutants from Primary Murine Hematopoietic Progenitor Cells

Molecular therapy, 2012-09, Vol.20 (9), p.10-10

2012

Volltextzugriff (PDF)

Reproducibility and Complications in Gene Searches: Linkage on Chromosome 6, Heterogeneity, Association, and Maternal Inheritance in Juvenile Myoclonic Epilepsy

American journal of human genetics, 2000-02, Vol.66 (2), p.508-516

2000

Volltextzugriff (PDF)

Mapping of a major susceptibility locus for Graves' disease (GD-1) to chromosome 14q31

The journal of clinical endocrinology and metabolism, 1997-05, Vol.82 (5), p.1645-1648

1997

Volltextzugriff (PDF)

First in vivo évidence of microRNA-induced fragile X mental retardation syndrome. Authors' reply

Molecular psychiatry, 2006, Vol.11 (7), p.616-617

2006

Volltextzugriff (PDF)

Association of HLA class II alleles in patients with juvenile myoclonic epilepsy compared with patients with other forms of adolescent-onset generalized epilepsy

Neurology, 1996-09, Vol.47 (3), p.750-755

1996

Volltextzugriff (PDF)

Genotypic and phenotypic correlations of DFNB1-related hearing impairment in the Midwestern United States

Archives of otolaryngology--head & neck surgery, 2003-08, Vol.129 (8), p.836

2003

Volltextzugriff (PDF)

374 Prospective genetic epidemiology of cognitive performance in the very old

Neurobiology of aging, 1996, Vol.17 (4), p.S93-S94

1996

Volltextzugriff (PDF)

Prospective study of the effect of APOE genotype on cognitive performance in the very old

European neuropsychopharmacology, 1996-06, Vol.6, p.145-145

1996

Volltextzugriff (PDF)

Apolipoprotein E allele ϵ4 in autopsy-confirmed Alzheimer's disease and cerebrovascular disease

Neurobiology of aging, 1994, Vol.15, p.S155-S155

1994

Volltextzugriff (PDF)

Cognitive impairment is not influenced by α1-antichymotrypsin genotype in the very old

Psychiatric genetics, 1996, Vol.6 (3), p.167

1996

Volltextzugriff (PDF)

A genome‐wide scan for juvenile rheumatoid arthritis in affected sibpair families provides evidence of linkage

Arthritis and rheumatism, 2004-09, Vol.50 (9), p.2920-2930

2004

Volltextzugriff (PDF)

1 – 25 von 44

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(40)
Mit Volltextzugriff
(35)

Publikationsform

Sprache

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Novel homo- and hemizygous mutations in EZH2 in myeloid malignancies

Evidence for linkage on 21q and 7q in a subset of autism characterized by developmental regression

Genotype-phenotype correlations in Rubinstein-Taybi syndrome

Linkage analysis for autism in a subset families with obsessive-compulsive behaviors: Evidence for an autism susceptibility gene on chromosome 1 and further support for susceptibility genes on chromosome 6 and 19

Identification of novel coding mutation in C1qA gene in an African–American pedigree with lupus and C1q deficiency

OP0212 Analysis of the immunochip in a large cohort of oligo- and polyarthritis juvenile idiopathic arthritis (JIA) cases confirms previous and identifies novel associations

Genome scan of idiopathic generalized epilepsy: Evidence for major susceptibility gene and modifying genes influencing the seizure type

Ethosuximide, valproic acid, and lamotrigine in childhood absence epilepsy: Initial monotherapy outcomes at 12 months

Response by Dr Molloy

Ethosuximide, Valproic Acid, and Lamotrigine in Childhood Absence Epilepsy

Gaucher's disease: identification of novel mutant alleles and genotype-phenotype relationships

Evidence for linkage on 21q and 7q in a subset of autism characterized by developmental regression

Characterization of neuronopathic Gaucher disease among ethnic Poles

Fucosyltransferase 2 Non-Secretor and Low Secretor Status Predicts Severe Outcomes in Premature Infants

Genotoxicity and Integration Pattern of Foamy Virus Vectors with Strong Internal Viral Enhancers in In Vitro Immortalized Mutants from Primary Murine Hematopoietic Progenitor Cells

Reproducibility and Complications in Gene Searches: Linkage on Chromosome 6, Heterogeneity, Association, and Maternal Inheritance in Juvenile Myoclonic Epilepsy

Mapping of a major susceptibility locus for Graves' disease (GD-1) to chromosome 14q31

First in vivo évidence of microRNA-induced fragile X mental retardation syndrome. Authors' reply

Association of HLA class II alleles in patients with juvenile myoclonic epilepsy compared with patients with other forms of adolescent-onset generalized epilepsy

Genotypic and phenotypic correlations of DFNB1-related hearing impairment in the Midwestern United States

374 Prospective genetic epidemiology of cognitive performance in the very old

Prospective study of the effect of APOE genotype on cognitive performance in the very old

Apolipoprotein E allele ϵ4 in autopsy-confirmed Alzheimer's disease and cerebrovascular disease

Cognitive impairment is not influenced by α1-antichymotrypsin genotype in the very old

A genome‐wide scan for juvenile rheumatoid arthritis in affected sibpair families provides evidence of linkage

Suchergebnisse filtern