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...

Characterization of PARP6 Function in Knockout Mice and Patients with Developmental Delay

Cells (Basel, Switzerland), 2021-05, Vol.10 (6), p.1289

2021

Volltextzugriff (PDF)

Infertility and abnormal cervical mucus in two sisters who are compound heterozygotes for the cystic fibrosis (CF) ΔF508 and R117H/7T mutations

Fertility and sterility, 2008-10, Vol.90 (4), p.1201.e19-1201.e22

2008

Volltextzugriff (PDF)

Array-based FMR1 sequencing and deletion analysis in patients with a fragile X syndrome-like phenotype

PloS one, 2010-03, Vol.5 (3), p.e9476-e9476

2010

Volltextzugriff (PDF)

Microsatellite instability in human solid tumors

Cancer, 1998-05, Vol.82 (10), p.1808-1820

1998

Volltextzugriff (PDF)

Characterization of a complex rearrangement involving duplication and deletion of 9p in an infant with craniofacial dysmorphism and cardiac anomalies

Molecular cytogenetics, 2012-07, Vol.5 (1), p.31-31

2012

Volltextzugriff (PDF)

Clinical report on long-term bone density after short-term EMF application

Bioelectromagnetics, 1998, Vol.19 (2), p.75-78

1998

Volltextzugriff (PDF)

Bone density changes in osteoporosis‐prone women exposed to pulsed electromagnetic fields (PEMFs)

Journal of bone and mineral research, 1990-05, Vol.5 (5), p.437-442

1990

Volltextzugriff (PDF)

Transposition and amplification of oncogene-related sequences in human neuroblastomas

Cell, 1983-12, Vol.35 (2), p.359-367

1983

Volltextzugriff (PDF)

TBX5 genetic testing validates strict clinical criteria for Holt-Oram syndrome

Pediatric research, 2005-11, Vol.58 (5), p.981-986

2005

Volltextzugriff (PDF)

Familial neuroblastoma: case reports, literature review, and etiologic considerations

Cancer, 1986-05, Vol.57 (9), p.1887-1893

1986

Volltextzugriff (PDF)

Design of the prostate, lung, colorectal and ovarian (PLCO) cancer screening trial

Controlled clinical trials, 2000-12, Vol.21 (6), p.273S-309S

2000

Volltextzugriff (PDF)

Substance abuse in Hawaii: Perspectives of key local human service organizations

Substance abuse, 1998-03, Vol.19 (1), p.7-22

1998

Volltextzugriff (PDF)

Novel 47.5-kb deletion in RAB27A results in severe Griscelli Syndrome Type 2

Molecular genetics and metabolism, 2010-09, Vol.101 (1), p.62-65

2010

Volltextzugriff (PDF)

Double Minute Chromosomes and the Homogeneously Staining Regions in Chromosomes of a Human Neuroblastoma Cell Line

Science (American Association for the Advancement of Science), 1977-11, Vol.198 (4318), p.739-741

1977

Volltextzugriff (PDF)

Infertility and abnormal cervical mucus in two sisters who are compound heterozygotes for the cystic fibrosis (CF) DeltaF508 and R117H/7T mutations

Fertility and sterility, 2008-10, Vol.90 (4), p.1201.e19-1201.e22

2008

Volltextzugriff (PDF)

Preimplantation genetic diagnosis of human congenital heart malformation and Holt–Oram syndrome

American journal of medical genetics, 2004-04, Vol.126A (1), p.93-98

2004

Volltextzugriff (PDF)

THE RELATIONSHIP BETWEEN WOLFE'S CLASSIFICATION MAMMOGRAMS, ACCEPTED BREAST CANCER RISK FACTORS, THE INCIDENCE OF BREAST CANCER

American journal of epidemiology, 1985-12, Vol.122 (6), p.994-1006

1985

Volltextzugriff (PDF)

Microsatellite instability differences between familial and sporadic ovarian cancers

Carcinogenesis (New York), 1996-09, Vol.17 (9), p.1799-1804

1996

Volltextzugriff (PDF)

Breast cancer prediction and the Wolfe classification of mammograms

JAMA : the journal of the American Medical Association, 1985-08, Vol.254 (8), p.1050

1985

Volltextzugriff (PDF)

CONGENITAL ABSENCE OF THE VAS DEFERENS: INCOMPLETE PENETRANCE OF CYSTIC FIBROSIS GENE MUTATIONS

The Journal of urology, 1997-11, Vol.158 (5), p.1794-1799

1997

Volltextzugriff (PDF)

Wolfe mammographic parenchymal patterns. A study of the masking hypothesis of Egan and Mosteller

Cancer, 1985-09, Vol.56 (6), p.1280-1286

1985

Volltextzugriff (PDF)

Optimal Iodine-131 Dose for Eliminating Hyperthyroidism in Graves' Disease

The Journal of nuclear medicine (1978), 1991-03, Vol.32 (3), p.411-416

1991

Volltextzugriff (PDF)

Amplified DNA with limited homology to myc cellular oncogene is shared by human neuroblastoma cell lines and a neuroblastoma tumour

Nature (London), 1983-09, Vol.305 (5931), p.245-248

1983

Volltextzugriff (PDF)

Pregnancy after embryo biopsy and coamplification of DNA from X and Y chromosomes

JAMA : the journal of the American Medical Association, 1992-08, Vol.268 (6), p.727

1992

Volltextzugriff (PDF)

Chromosomes, Genes, and Cancer: A Classification of Chromosome Abnormalities in Cancer

JNCI : Journal of the National Cancer Institute, 1983-12, Vol.71 (6), p.1107-1114

Gilbert, F

1983

Volltextzugriff (PDF)

1 – 25 von 447

Suche als RSS-Feed

Aktive Filter

PublikationsformArtikel

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(368)
Mit Volltextzugriff
(357)

Sprache

Erscheinungsjahr

n.n

Thema

Science & Technology
(246)
Life Sciences & Biomedicine
(198)
Humans
(188)
Female
(104)
Biological And Medical Sciences
(84)
Male
(84)
Medical Sciences
(66)
Animals
(57)
Middle Aged
(56)
Adult
(55)
Physical Sciences
(35)
Aged
(31)
Genetics & Heredity
(27)
Oncology
(27)
Internal Medicine
(20)
Fundamental And Applied Biological Sciences. Psychology
(19)
Infectious Diseases
(19)
Mice
(19)
Tumors
(19)
Cardiology
(18)

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

Characterization of PARP6 Function in Knockout Mice and Patients with Developmental Delay

Infertility and abnormal cervical mucus in two sisters who are compound heterozygotes for the cystic fibrosis (CF) ΔF508 and R117H/7T mutations

Array-based FMR1 sequencing and deletion analysis in patients with a fragile X syndrome-like phenotype

Microsatellite instability in human solid tumors

Characterization of a complex rearrangement involving duplication and deletion of 9p in an infant with craniofacial dysmorphism and cardiac anomalies

Clinical report on long-term bone density after short-term EMF application

Bone density changes in osteoporosis‐prone women exposed to pulsed electromagnetic fields (PEMFs)

Transposition and amplification of oncogene-related sequences in human neuroblastomas

TBX5 genetic testing validates strict clinical criteria for Holt-Oram syndrome

Familial neuroblastoma: case reports, literature review, and etiologic considerations

Design of the prostate, lung, colorectal and ovarian (PLCO) cancer screening trial

Substance abuse in Hawaii: Perspectives of key local human service organizations

Novel 47.5-kb deletion in RAB27A results in severe Griscelli Syndrome Type 2

Double Minute Chromosomes and the Homogeneously Staining Regions in Chromosomes of a Human Neuroblastoma Cell Line

Infertility and abnormal cervical mucus in two sisters who are compound heterozygotes for the cystic fibrosis (CF) DeltaF508 and R117H/7T mutations

Preimplantation genetic diagnosis of human congenital heart malformation and Holt–Oram syndrome

THE RELATIONSHIP BETWEEN WOLFE'S CLASSIFICATION MAMMOGRAMS, ACCEPTED BREAST CANCER RISK FACTORS, THE INCIDENCE OF BREAST CANCER

Microsatellite instability differences between familial and sporadic ovarian cancers

Breast cancer prediction and the Wolfe classification of mammograms

CONGENITAL ABSENCE OF THE VAS DEFERENS: INCOMPLETE PENETRANCE OF CYSTIC FIBROSIS GENE MUTATIONS

Wolfe mammographic parenchymal patterns. A study of the masking hypothesis of Egan and Mosteller

Optimal Iodine-131 Dose for Eliminating Hyperthyroidism in Graves' Disease

Amplified DNA with limited homology to myc cellular oncogene is shared by human neuroblastoma cell lines and a neuroblastoma tumour

Pregnancy after embryo biopsy and coamplification of DNA from X and Y chromosomes

Chromosomes, Genes, and Cancer: A Classification of Chromosome Abnormalities in Cancer

Aktive Filter

Suchergebnisse filtern