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...

Expansion of Genetic Services Utilizing a General Genetic Counseling Clinic

Journal of genetic counseling, 2014-02, Vol.23 (1), p.64-71

2014

Volltextzugriff (PDF)

Lack of interest by nonpregnant couples in population-based cystic fibrosis carrier screening

American journal of human genetics, 1996-03, Vol.58 (3), p.617-627

1996

Volltextzugriff (PDF)

Teaching about cystic fibrosis carrier screening by using written and video information

American journal of human genetics, 1995-07, Vol.57 (1), p.171-181

1995

Volltextzugriff (PDF)

Speech delay and autism spectrum behaviors are frequently associated with duplication of the 7q11.23 Williams-Beuren syndrome region

Genetics in medicine, 2007-07, Vol.9 (7), p.427-441

2007

Volltextzugriff (PDF)

A Recurrent RNA-Splicing Mutation in the SEDL Gene Causes X-Linked Spondyloepiphyseal Dysplasia Tarda

American journal of human genetics, 2001-06, Vol.68 (6), p.1398-1407

2001

Volltextzugriff (PDF)

Developmental Change in Human Intestinal Alkaline Phosphatase

Proceedings of the National Academy of Sciences - PNAS, 1978-08, Vol.75 (8), p.3909-3912

1978

Volltextzugriff (PDF)

Presymptomatic testing for adult onset polycystic kidney disease in at-risk kidney transplant donors

American journal of medical genetics, 1991-09, Vol.40 (4), p.425-428

1991

Volltextzugriff (PDF)

Alopecia/mental retardation syndrome

American journal of medical genetics, 1995-08, Vol.58 (2), p.123-124

1995

Volltextzugriff (PDF)

Whose DNA is it anyway? Relationships between families and researchers

American journal of medical genetics, 1993-08, Vol.47 (2), p.257-260

1993

Volltextzugriff (PDF)

Utilization and evaluation of living-related donors for patients with adult polycystic kidney disease

American journal of medical genetics, 1992-11, Vol.44 (4), p.409-412

1992

Volltextzugriff (PDF)

Maternal cocaine abuse and fetal anomalies: evidence for teratogenic effects of cocaine

Southern medical journal (Birmingham, Ala.), 1991-04, Vol.84 (4), p.498-499

1991

Volltextzugriff (PDF)

The oral microbiome – an update for oral healthcare professionals

British dental journal, 2016-11, Vol.221 (10), p.657-666

2016

Volltextzugriff (PDF)

Trends in Data Locality Abstractions for HPC Systems

IEEE transactions on parallel and distributed systems, 2017-10, Vol.28 (10), p.3007-3020

2017

Volltextzugriff (PDF)

TRICC-C: Nintedanib vs. placebo in patients receiving mFOLFOX6 for metastatic, chemorefractory colorectal cancer: Final results from the randomized phase II trial of the AIO

Annals of oncology, 2018-10, Vol.29 Suppl 8, p.viii188-viii189

2018

Volltextzugriff (PDF)

The Cognitive and Behavioral Phenotypes of Individuals with CHRNA7 Duplications

Journal of autism and developmental disorders, 2017-03, Vol.47 (3), p.549-562

2017

Volltextzugriff (PDF)

424P Avelumab added to FOLFIRI plus cetuximab followed by avelumab maintenance in patients with previously untreated RAS wild-type colorectal cancer: The phase-II FIRE-6 (AIO KRK-0118)

Annals of oncology, 2022-09, Vol.33, p.S729

2022

Volltextzugriff (PDF)

Decoding the diagnostic and therapeutic potential of microbiota using pan-body pan-disease microbiomics

Nature communications, 2024-09, Vol.15 (1), p.8261-13, Article 8261

2024

Volltextzugriff (PDF)

Abstract P4-14-06: Neoadjuvant chemotherapy with docetaxel, carboplatin and weekly trastuzumab (TCH) is active in HER2-positive early breast cancer: Results after a median follow-up of over 4 years

Cancer research (Chicago, Ill.), 2016-02, Vol.76 (4_Supplement), p.P4-P4-14-06

2016

Volltextzugriff (PDF)

Erratum to: The Cognitive and Behavioral Phenotypes of Individuals with CHRNA7 Duplications

Journal of autism and developmental disorders, 2017-03, Vol.47 (3), p.563-563

2017

Volltextzugriff (PDF)

Small rare recurrent deletions and reciprocal duplications in 2q21.1, including brain-specific ARHGEF4 and GPR148

Human molecular genetics, 2012-08, Vol.21 (15), p.3345-3355

2012

Volltextzugriff (PDF)

564PTRICC-C: Nintedanib vs. placebo in patients receiving mFOLFOX6 for metastatic, chemorefractory colorectal cancer: Final results from the randomized phase II trial of the AIO

Annals of oncology, 2018-10, Vol.29 (suppl_8)

2018

Volltextzugriff (PDF)

Recombinant Glycoproteins That Inhibit Complement Activation and Also Bind the Selectin Adhesion Molecules

The Journal of biological chemistry, 1999-04, Vol.274 (16), p.11237-11244

1999

Volltextzugriff (PDF)

System Integration of Tightly-Coupled Reconfigurable Processor Arrays and Evaluation of Buffer Size Effects on Their Performance

2009 International Conference on Parallel Processing Workshops, 2009, p.528-534

2009

Volltextzugriff (PDF)

Diagnostic dilemma caused by overlapping features of Prader-Willi syndrome and trisomy 18 during infancy

The Journal of pediatrics, 2000-01, Vol.136 (1), p.135-136

2000

Volltextzugriff (PDF)

1 – 25 von 29

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(22)
Mit Volltextzugriff
(28)

Publikationsform

Sprache

Englisch
(27)
Deutsch
(2)

Erscheinungsjahr

n.n

Thema

Science & Technology
(19)
Humans
(18)
Life Sciences & Biomedicine
(15)
Female
(12)
Genetics & Heredity
(11)
Male
(11)
Biological And Medical Sciences
(9)
Adult
(7)
Medical Sciences
(6)
Child
(4)
Child, Preschool
(4)
Bioethics
(3)
Fundamental And Applied Biological Sciences. Psychology
(3)
Genetic Counseling
(3)
Genetics
(3)
Genomes
(3)
Infant, Newborn
(3)
Kidneys
(3)
Pediatrics
(3)
Pedigree
(3)

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

Expansion of Genetic Services Utilizing a General Genetic Counseling Clinic

Lack of interest by nonpregnant couples in population-based cystic fibrosis carrier screening

Teaching about cystic fibrosis carrier screening by using written and video information

Speech delay and autism spectrum behaviors are frequently associated with duplication of the 7q11.23 Williams-Beuren syndrome region

A Recurrent RNA-Splicing Mutation in the SEDL Gene Causes X-Linked Spondyloepiphyseal Dysplasia Tarda

Developmental Change in Human Intestinal Alkaline Phosphatase

Presymptomatic testing for adult onset polycystic kidney disease in at-risk kidney transplant donors

Alopecia/mental retardation syndrome

Whose DNA is it anyway? Relationships between families and researchers

Utilization and evaluation of living-related donors for patients with adult polycystic kidney disease

Maternal cocaine abuse and fetal anomalies: evidence for teratogenic effects of cocaine

The oral microbiome – an update for oral healthcare professionals

Trends in Data Locality Abstractions for HPC Systems

TRICC-C: Nintedanib vs. placebo in patients receiving mFOLFOX6 for metastatic, chemorefractory colorectal cancer: Final results from the randomized phase II trial of the AIO

The Cognitive and Behavioral Phenotypes of Individuals with CHRNA7 Duplications

424P Avelumab added to FOLFIRI plus cetuximab followed by avelumab maintenance in patients with previously untreated RAS wild-type colorectal cancer: The phase-II FIRE-6 (AIO KRK-0118)

Decoding the diagnostic and therapeutic potential of microbiota using pan-body pan-disease microbiomics

Thirteen New Patients with Guanidinoacetate Methyltransferase Deficiency and Functional Characterization of Nineteen Novel Missense Variants in the GAMT Gene

Abstract P4-14-06: Neoadjuvant chemotherapy with docetaxel, carboplatin and weekly trastuzumab (TCH) is active in HER2-positive early breast cancer: Results after a median follow-up of over 4 years

Erratum to: The Cognitive and Behavioral Phenotypes of Individuals with CHRNA7 Duplications

Small rare recurrent deletions and reciprocal duplications in 2q21.1, including brain-specific ARHGEF4 and GPR148

564PTRICC-C: Nintedanib vs. placebo in patients receiving mFOLFOX6 for metastatic, chemorefractory colorectal cancer: Final results from the randomized phase II trial of the AIO

Recombinant Glycoproteins That Inhibit Complement Activation and Also Bind the Selectin Adhesion Molecules

System Integration of Tightly-Coupled Reconfigurable Processor Arrays and Evaluation of Buffer Size Effects on Their Performance

Diagnostic dilemma caused by overlapping features of Prader-Willi syndrome and trisomy 18 during infancy

Suchergebnisse filtern