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...

Site-Specific Integration by Adeno-Associated Virus

Proceedings of the National Academy of Sciences - PNAS, 1990-03, Vol.87 (6), p.2211-2215

1990

Volltextzugriff (PDF)

Human Gene Mapping and Cancer Biology

Ciba Foundation Symposium 66 ‐ Human Genetics: Possibilities and Realities, 1979, p.283-309

1979

Volltextzugriff (PDF)

Genetic recombination and disease

Cold Spring Harbor Symposia on Quantitative Biology, 1986, Vol.51 Pt 1, p.191-194

Siniscalco, M

1986

Volltextzugriff (PDF)

Population genomics in Sardinia: a novel approach to hunt for genomic combinations underlying complex traits and diseases

Cytogenetic and genome research, 1999-01, Vol.86 (2), p.148-152

1999

Volltextzugriff (PDF)

Cytological Mapping of the Human Glucose-6-phosphate Dehydrogenase Gene Distal to the Fragile-X Site Suggests a High Rate of Meiotic Recombination across This Site

Proceedings of the National Academy of Sciences - PNAS, 1984-12, Vol.81 (24), p.7855-7859

1984

Volltextzugriff (PDF)

Chromosomes of Older Humans are More Prone to Aminopterine-Induced Breakage

Proceedings of the National Academy of Sciences - PNAS, 1989-02, Vol.86 (4), p.1302-1306

1989

Volltextzugriff (PDF)

Somatic cell hybrids, surface antigens, and monoclonal antibodies

Transplantation proceedings, 1979-12, Vol.11 (4), p.1701-1705

Siniscalco, M

1979

Volltextzugriff (PDF)

Subregional mapping of the human lymphocyte-specific protein tyrosine kinase gene (LCK) to 1p35-->p34.3 and its position relative to the 1p marker D1S57

Cytogenetic and genome research, 1994-01, Vol.67 (3), p.187-189

1994

Volltextzugriff (PDF)

Mapping of the gene coding for a paraneoplastic encephalomyelitis antigen (HuD) to human chromosome site 1p34

Cytogenetic and genome research, 1994-01, Vol.65 (3), p.177-178

1994

Volltextzugriff (PDF)

A Human Autosomal Phosphoglycerate Kinase Locus Maps near the HLA Cluster

Proceedings of the National Academy of Sciences - PNAS, 1984-05, Vol.81 (10), p.3167-3169

1984

Volltextzugriff (PDF)

Concurrent mapping of an adenovirus 5/SV40 integration site and the U1 snRNA cluster (RNU1) within 400 kb of the chromosome region 1p36.1

Cytogenetic and genome research, 1994, Vol.67 (1), p.37-40

1994

Volltextzugriff (PDF)

A 9.1-kb Gap in the Genome Reference Map Is Shown to Be a Stable Deletion/Insertion Polymorphism of Ancestral Origin

Genomics (San Diego, Calif.), 2002-12, Vol.80 (6), p.585-592

2002

Volltextzugriff (PDF)

Human genome mapping and its medical perspectives

Southeast Asian journal of tropical medicine and public health, 1997, Vol.28 Suppl 2, p.25-46

Siniscalco, M

1997

Volltextzugriff (PDF)

Giorgio Filippi, April 4, 1935-January 19, 1996

American journal of medical genetics, 1997-01, Vol.68 (1), p.94-97

Siniscalco, Marcello

1997

Volltextzugriff (PDF)

The human genes for hemophilia A and hemophilia B flank the X chromosome fragile site at Xq27.3

The EMBO journal, 1985-03, Vol.4 (3), p.725-729

1985

Volltextzugriff (PDF)

In situ mapping of the gene coding for a leucine zipper DNA binding protein (CDR62) to 16p12–16p13.1

Genomics (San Diego, Calif.), 1992-08, Vol.13 (4), p.1340-1342

1992

Volltextzugriff (PDF)

A Novel Approach to Search for Identity by Descent in Small Samples of Patients and Controls from the Same Mendelian Breeding Unit: A Pilot Study on Myopia

Human heredity, 2001-01, Vol.52 (4), p.183-190

2001

Volltextzugriff (PDF)

A plea to search for deletion polymorphism through genome scans in populations

Trends in genetics, 2000-10, Vol.16 (10), p.435-437

2000

Volltextzugriff (PDF)

Distribution of Serum Haptoglobin Types in Some Italian Populations

Ciba Foundation Symposium ‐ Steroid Hormones and Tumour Growth (Book I of Colloquia on Endocrinology), 1959, p.220-245

1959

Volltextzugriff (PDF)

Effect of a Single Gene Difference on the Pattern of Some Physical Measurements

Ciba Foundation Symposium ‐ Steroid Hormones and Tumour Growth (Book I of Colloquia on Endocrinology), 1959, p.205-219

1959

Volltextzugriff (PDF)

Approaches to human linkage

Progress in medical genetics, 1979, Vol.3, p.221

Siniscalco, M

1979

Volltextzugriff (PDF)

The myoblast defect identified in Duchenne muscular dystrophy is not a primary expression of the DMD mutation: clonal analysis of myoblasts from five double heterozygotes for two X-linked loci: DMD and G6PD

Human genetics, 1986-09, Vol.74 (1), p.74-80

1986

Volltextzugriff (PDF)

Human gene mapping and cancer biology

Ciba Foundation symposium, 1979-06 (66), p.283

Siniscalco, M

1979

Volltextzugriff (PDF)

An anonymous single copy X-chromosome clone DXS92, from Xq26–27, identifies two frequent RFLPs

Nucleic acids research, 1985-10, Vol.13 (20), p.7540-7540

1985

Volltextzugriff (PDF)

An anonymous single copy X-chromosome clone DXS91, from Xq11-q13, identifies a moderately frequent RFLP

Nucleic acids research, 1985-10, Vol.13 (20), p.7539-7539

1985

Volltextzugriff (PDF)

1 – 25 von 212

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(155)
Mit Volltextzugriff
(142)

Publikationsform

1 weiteren anzeigen...

Weniger anzeigen...

Sprache

Erscheinungsjahr

n.n

Thema

Humans
(117)
Science & Technology
(100)
Life Sciences & Biomedicine
(83)
Female
(50)
Male
(47)
Chromosome Mapping
(41)
Animals
(39)
Genetics & Heredity
(39)
Biological And Medical Sciences
(34)
Genetic Linkage
(34)
Mice
(28)
X Chromosome
(27)
Sex Chromosomes
(24)
Fundamental And Applied Biological Sciences. Psychology
(22)
Genes
(22)
Cell Biology
(18)
Hybrid Cells
(18)
Italy
(17)
Old Medline
(17)
Pedigree
(17)

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(2)

Menü

Weitere Dienste

Einstellungen

Site-Specific Integration by Adeno-Associated Virus

Human Gene Mapping and Cancer Biology

Genetic recombination and disease

Population genomics in Sardinia: a novel approach to hunt for genomic combinations underlying complex traits and diseases

Cytological Mapping of the Human Glucose-6-phosphate Dehydrogenase Gene Distal to the Fragile-X Site Suggests a High Rate of Meiotic Recombination across This Site

Chromosomes of Older Humans are More Prone to Aminopterine-Induced Breakage

Somatic cell hybrids, surface antigens, and monoclonal antibodies

Subregional mapping of the human lymphocyte-specific protein tyrosine kinase gene (LCK) to 1p35-->p34.3 and its position relative to the 1p marker D1S57

Mapping of the gene coding for a paraneoplastic encephalomyelitis antigen (HuD) to human chromosome site 1p34

A Human Autosomal Phosphoglycerate Kinase Locus Maps near the HLA Cluster

Concurrent mapping of an adenovirus 5/SV40 integration site and the U1 snRNA cluster (RNU1) within 400 kb of the chromosome region 1p36.1

A 9.1-kb Gap in the Genome Reference Map Is Shown to Be a Stable Deletion/Insertion Polymorphism of Ancestral Origin

Human genome mapping and its medical perspectives

Giorgio Filippi, April 4, 1935-January 19, 1996

The human genes for hemophilia A and hemophilia B flank the X chromosome fragile site at Xq27.3

In situ mapping of the gene coding for a leucine zipper DNA binding protein (CDR62) to 16p12–16p13.1

A Novel Approach to Search for Identity by Descent in Small Samples of Patients and Controls from the Same Mendelian Breeding Unit: A Pilot Study on Myopia

A plea to search for deletion polymorphism through genome scans in populations

Distribution of Serum Haptoglobin Types in Some Italian Populations

Effect of a Single Gene Difference on the Pattern of Some Physical Measurements

Approaches to human linkage

The myoblast defect identified in Duchenne muscular dystrophy is not a primary expression of the DMD mutation: clonal analysis of myoblasts from five double heterozygotes for two X-linked loci: DMD and G6PD

Human gene mapping and cancer biology

An anonymous single copy X-chromosome clone DXS92, from Xq26–27, identifies two frequent RFLPs

An anonymous single copy X-chromosome clone DXS91, from Xq11-q13, identifies a moderately frequent RFLP

Suchergebnisse filtern