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...

Verstehende Soziologie: Lehrbuch

Helle, Horst Jürgen

Reprint 2016 edition., 2016

Volltextzugriff (PDF)

O-(2-[18F]fluoroethyl)-L-tyrosine and L-[methyl-11C]methionine uptake in brain tumours: initial results of a comparative study

European journal of nuclear medicine, 2000-05, Vol.27 (5), p.542-549

2000

Volltextzugriff (PDF)

Diagnosis of haploidy and triploidy based on measurement of gene copy number by real-time PCR

Human mutation, 2000-11, Vol.16 (5), p.431-436

2000

Volltextzugriff (PDF)

Keramik

Seventh Edition., 2007

Volltextzugriff (PDF)

Seven novel and four recurrent point mutations in the factor VIII (F8C) gene

Human mutation, 2002-01, Vol.19 (1), p.84-84

2002

Volltextzugriff (PDF)

Seven novel and four recurrent point mutations in the factor VIII (F8C) gene

Human mutation, 2001-12, Vol.18 (6), p.546-546

2001

Volltextzugriff (PDF)

FFU complex : an analysis of 491 cases

Human genetics, 1993-05, Vol.91 (4), p.347-356

1993

Volltextzugriff (PDF)

Screening the 3′ region of the polycystic kidney disease 1 (PKD1) gene in 41 Bulgarian and Australian kindreds reveals a prevalence of protein truncating mutations

Human mutation, 2000-08, Vol.16 (2), p.166-174

2000

Volltextzugriff (PDF)

thalassemia in the German population: Mediterranean, Asian and novel mutations

Human mutation, 1999, Vol.13 (3), p.258-258

1999

Volltextzugriff (PDF)

The importance of clinical documentation in genetic studies of male infertility

Human genetics, 1995-10, Vol.96 (4), p.500-501

1995

Volltextzugriff (PDF)

Mutational-screening in the factor VIII gene resulting in the identification of three novel mutations, one of which is a donor splice mutation

Human mutation, 1999, Vol.13 (6), p.504-504

1999

Volltextzugriff (PDF)

Raine syndrome: report of a family with three affected sibs and further delineation of the syndrome

Clinical dysmorphology, 2003-07, Vol.12 (3), p.153-160

2003

Volltextzugriff (PDF)

Phenylketonuria: detection of a frequent haplotype 4 allele mutation

Human genetics, 1989-12, Vol.84 (1), p.95-96

1989

Volltextzugriff (PDF)

Genetic factors in lissencephaly syndromes: a review

Child's nervous system, 1993-11, Vol.9 (7), p.413-417

1993

Volltextzugriff (PDF)

Molecular analysis of PKU haplotypes in the population of Southern Poland

Human genetics, 1991, Vol.86 (3), p.292-294

1991

Volltextzugriff (PDF)

Phenylketonuria in Poland : 66% of PKU alleles are caused by three mutations

Human genetics, 1991-11, Vol.88 (1), p.91-94

1991

Volltextzugriff (PDF)

GGT-Cre mice for tissue-specific gene ablation in proximal kidney tubules

GBM Annual Fall meeting M nster 2004, 2004-09, Vol.2004 (Fall), Article 669

2004

Volltextzugriff (PDF)

Low rates of pregnancy termination for prenatally diagnosed Klinefelter syndrome and other sex chromosome polysomies

American journal of medical genetics, 1998-12, Vol.80 (4), p.330-334

1998

Volltextzugriff (PDF)

Globin gene deletion causes ?-thalassemia syndromes in two German families

Human genetics, 1984, Vol.68 (3), p.260-263

1984

Volltextzugriff (PDF)

Submicroscopic deletion in 14q32.3 through a de novo tandem translocation between 14q and 21p

American journal of medical genetics, 1998-12, Vol.80 (5), p.443-447

1998

Volltextzugriff (PDF)

Variability of bacterial gene-directed enzyme production in human genetically deficient cells

Human genetics, 1979-01, Vol.46 (2), p.209-217

1979

Volltextzugriff (PDF)

On procaryotic gene expression in eucaryotic systems

Human genetics, 1980-06, Vol.54 (3), p.289-302

1980

Volltextzugriff (PDF)

Neues und Fremdes im deutschen Wortschatz: Aktueller lexikalischer Wandel

Stickel, Gerhard

2019

Volltextzugriff (PDF)

China: Promise or Threat?: A Comparison of Cultures

Helle, Horst J

2017

Volltextzugriff (PDF)

Pharmacodynamics and Pharmacokinetics of Inhaled Iloprost, Aerosolized by Three Different Devices, in Severe Pulmonary Hypertension

Chest, 2003-10, Vol.124 (4), p.1294-1304

2003

Volltextzugriff (PDF)

1 – 25 von 70

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(55)
Mit Volltextzugriff
(62)

Publikationsform

Artikel
(62)
Bücher
(8)

Sprache

Englisch
(61)
Deutsch
(10)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Verstehende Soziologie: Lehrbuch

O-(2-[18F]fluoroethyl)-L-tyrosine and L-[methyl-11C]methionine uptake in brain tumours: initial results of a comparative study

Diagnosis of haploidy and triploidy based on measurement of gene copy number by real-time PCR

Keramik

Seven novel and four recurrent point mutations in the factor VIII (F8C) gene

Seven novel and four recurrent point mutations in the factor VIII (F8C) gene

FFU complex : an analysis of 491 cases

Screening the 3′ region of the polycystic kidney disease 1 (PKD1) gene in 41 Bulgarian and Australian kindreds reveals a prevalence of protein truncating mutations

thalassemia in the German population: Mediterranean, Asian and novel mutations

The importance of clinical documentation in genetic studies of male infertility

Mutational-screening in the factor VIII gene resulting in the identification of three novel mutations, one of which is a donor splice mutation

Raine syndrome: report of a family with three affected sibs and further delineation of the syndrome

Phenylketonuria: detection of a frequent haplotype 4 allele mutation

Genetic factors in lissencephaly syndromes: a review

Molecular analysis of PKU haplotypes in the population of Southern Poland

Phenylketonuria in Poland : 66% of PKU alleles are caused by three mutations

GGT-Cre mice for tissue-specific gene ablation in proximal kidney tubules

Low rates of pregnancy termination for prenatally diagnosed Klinefelter syndrome and other sex chromosome polysomies

Globin gene deletion causes ?-thalassemia syndromes in two German families

Submicroscopic deletion in 14q32.3 through a de novo tandem translocation between 14q and 21p

Variability of bacterial gene-directed enzyme production in human genetically deficient cells

On procaryotic gene expression in eucaryotic systems

Neues und Fremdes im deutschen Wortschatz: Aktueller lexikalischer Wandel

China: Promise or Threat?: A Comparison of Cultures

Pharmacodynamics and Pharmacokinetics of Inhaled Iloprost, Aerosolized by Three Different Devices, in Severe Pulmonary Hypertension

Suchergebnisse filtern