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...

Enhancement of leukotriene C 4 release from primate airway macrophages by cellular interactions

British journal of pharmacology, 1989-10, Vol.98 (2), p.637-645

1989

Volltextzugriff (PDF)

Enhancement of leukotriene C4 release from primate airway macrophages by cellular interactions

British journal of pharmacology, 1989-10, Vol.98 (2), p.637-645

1989

Volltextzugriff (PDF)

Laboratory infection of primates with Ascaris suum to provide a model of allergic bronchoconstriction

Clinical and experimental immunology, 1983-01, Vol.54 (2), p.469-476

1983

Volltextzugriff (PDF)

The anti-allergic effects of FPL 52694

International archives of allergy and applied immunology, 1985-01, Vol.76 (2), p.188-190

1985

Volltextzugriff (PDF)

Cairo consensus on the IVF laboratory environment and air quality: report of an expert meeting

Reproductive biomedicine online, 2018-06, Vol.36 (6), p.658-674

2018

Volltextzugriff (PDF)

Curious bivalves: Systematic utility and unusual properties of anomalodesmatan mitochondrial genomes

Molecular phylogenetics and evolution, 2017-05, Vol.110, p.60-72

2017

Volltextzugriff (PDF)

Regional assessment of lake ecological states using Landsat: A classification scheme for alkaline–saline, flamingo lakes in the East African Rift Valley

International journal of applied earth observation and geoinformation, 2015-08, Vol.40, p.100-108

2015

Volltextzugriff (PDF)

Remote sensing the hydrological variability of Tanzania's Lake Natron, a vital Lesser Flamingo breeding site under threat

Ecohydrology & Hydrobiology, 2013, Vol.13 (2), p.148-158

2013

Volltextzugriff (PDF)

G.P.11.11 Myasthenic syndrome due to defects in rapsyn: Clinical and molecular findings in 39 patients

Neuromuscular disorders : NMD, 2009-09, Vol.19 (8), p.626-627

2009

Volltextzugriff (PDF)

Psoas compartment block for lower extremity surgery

British journal of anaesthesia : BJA, 2009-05, Vol.102 (5), p.721-722

2009

Volltextzugriff (PDF)

Frame-Shift Deletions in Patients with Duchenne and Becker Muscular Dystrophy

Science (American Association for the Advancement of Science), 1988-11, Vol.242 (4879), p.755-759

1988

Volltextzugriff (PDF)

Genetic heterogeneity in X-linked amelogenesis imperfecta

Genomics (San Diego, Calif.), 1992-11, Vol.14 (3), p.567-573

1992

Volltextzugriff (PDF)

X linked neonatal centronuclear/myotubular myopathy: evidence for linkage to Xq28 DNA marker loci

Journal of medical genetics, 1990-05, Vol.27 (5), p.284-287

1990

Volltextzugriff (PDF)

X-linked hypohidrotic ectodermal dysplasia: localization within the region Xq11-21.1 by linkage analysis and implications for carrier detection and prenatal diagnosis

American journal of human genetics, 1988-07, Vol.43 (1), p.75-85

1988

Volltextzugriff (PDF)

Economic Analysis of an Aquaponic System for the Integrated Production of Rainbow Trout and Plants

International journal of recirculating aquaculture, 2000-06, Vol.1 (1)

2000

Volltextzugriff (PDF)

Assignment of Emery-Dreifuss muscular dystrophy to the distal region of Xq28: the results of a collaborative study

American journal of human genetics, 1991-03, Vol.48 (3), p.468-480

1991

Volltextzugriff (PDF)

Localisation of the Becker muscular dystrophy gene on the short arm of the X chromosome by linkage to cloned DNA sequences

Human genetics, 1984-01, Vol.67 (1), p.6-17

1984

Volltextzugriff (PDF)

Recognition and reanalysis of a cell line from a manifesting female with X linked hypohidrotic ectodermal dysplasia and an X; autosome balanced translocation

Journal of medical genetics, 1988-06, Vol.25 (6), p.383-386

1988

Volltextzugriff (PDF)

Becker muscular dystrophy: correlation of deletion type with clinical severity

Journal of medical genetics, 1990-04, Vol.27 (4), p.236-239

1990

Volltextzugriff (PDF)

X-linked hypohidrotic ectodermal dysplasia: DNA probe linkage analysis and gene localization

Human genetics, 1987-04, Vol.75 (4), p.378-380

1987

Volltextzugriff (PDF)

Localisation of the gene for Emery-Dreifuss muscular dystrophy to the distal long arm of the X chromosome

Journal of medical genetics, 1986-12, Vol.23 (6), p.596-598

1986

Volltextzugriff (PDF)

Genetic linkage between Becker muscular dystrophy and a polymorphic DNA sequence on the short arm of the X chromosome

Journal of medical genetics, 1983-08, Vol.20 (4), p.255-258

1983

Volltextzugriff (PDF)

Localisation of the gene for Hunter syndrome on the long arm of X chromosome

Human genetics, 1986-12, Vol.74 (4), p.391-398

1986

Volltextzugriff (PDF)

Molecular deletion analysis in Duchenne muscular dystrophy

Journal of medical genetics, 1986-12, Vol.23 (6), p.509-515

1986

Volltextzugriff (PDF)

Duchenne muscular dystrophy with adrenal insufficiency and glycerol kinase deficiency: high resolution cytogenetic analysis with molecular, biochemical, and clinical studies

Journal of medical genetics, 1986-12, Vol.23 (6), p.501-508

1986

Volltextzugriff (PDF)

1 – 25 von 40

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(38)
Mit Volltextzugriff
(35)

Publikationsform

Artikel
(40)

Sprache

Englisch
(40)

Erscheinungsjahr

n.n

Thema

Science & Technology
(32)
Life Sciences & Biomedicine
(30)
Humans
(26)
Biological And Medical Sciences
(21)
Medical Sciences
(21)
Male
(20)
Female
(19)
Genetics & Heredity
(19)
Genetic Linkage
(17)
X Chromosome
(17)
Pedigree
(15)
Chromosome Mapping
(13)
Muscular Dystrophies - Genetics
(11)
Neurology
(11)
Diseases Of Striated Muscles. Neuromuscular Diseases
(9)
Genetic Carrier Screening
(8)
Chromosome Deletion
(7)
Animals
(6)
Genetic Markers
(6)
Polymorphism, Genetic
(6)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Enhancement of leukotriene C 4 release from primate airway macrophages by cellular interactions

Enhancement of leukotriene C4 release from primate airway macrophages by cellular interactions

Laboratory infection of primates with Ascaris suum to provide a model of allergic bronchoconstriction

The anti-allergic effects of FPL 52694

Cairo consensus on the IVF laboratory environment and air quality: report of an expert meeting

Curious bivalves: Systematic utility and unusual properties of anomalodesmatan mitochondrial genomes

Regional assessment of lake ecological states using Landsat: A classification scheme for alkaline–saline, flamingo lakes in the East African Rift Valley

Remote sensing the hydrological variability of Tanzania's Lake Natron, a vital Lesser Flamingo breeding site under threat

G.P.11.11 Myasthenic syndrome due to defects in rapsyn: Clinical and molecular findings in 39 patients

Psoas compartment block for lower extremity surgery

Frame-Shift Deletions in Patients with Duchenne and Becker Muscular Dystrophy

Genetic heterogeneity in X-linked amelogenesis imperfecta

X linked neonatal centronuclear/myotubular myopathy: evidence for linkage to Xq28 DNA marker loci

X-linked hypohidrotic ectodermal dysplasia: localization within the region Xq11-21.1 by linkage analysis and implications for carrier detection and prenatal diagnosis

Economic Analysis of an Aquaponic System for the Integrated Production of Rainbow Trout and Plants

Assignment of Emery-Dreifuss muscular dystrophy to the distal region of Xq28: the results of a collaborative study

Localisation of the Becker muscular dystrophy gene on the short arm of the X chromosome by linkage to cloned DNA sequences

Recognition and reanalysis of a cell line from a manifesting female with X linked hypohidrotic ectodermal dysplasia and an X; autosome balanced translocation

Becker muscular dystrophy: correlation of deletion type with clinical severity

X-linked hypohidrotic ectodermal dysplasia: DNA probe linkage analysis and gene localization

Localisation of the gene for Emery-Dreifuss muscular dystrophy to the distal long arm of the X chromosome

Genetic linkage between Becker muscular dystrophy and a polymorphic DNA sequence on the short arm of the X chromosome

Localisation of the gene for Hunter syndrome on the long arm of X chromosome

Molecular deletion analysis in Duchenne muscular dystrophy

Duchenne muscular dystrophy with adrenal insufficiency and glycerol kinase deficiency: high resolution cytogenetic analysis with molecular, biochemical, and clinical studies

Suchergebnisse filtern