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...

Extensive Normal Copy Number Variation of a β-Defensin Antimicrobial-Gene Cluster

American journal of human genetics, 2003-09, Vol.73 (3), p.591-600

2003

Volltextzugriff (PDF)

Transient neonatal diabetes: widening the understanding of the etiopathogenesis of diabetes

Diabetes (New York, N.Y.), 2000-08, Vol.49 (8), p.1359-1366

2000

Volltextzugriff (PDF)

Repetitive DNA and chromosomal rearrangements: speciation-related events in plant genomes

Cytogenetic and genome research, 2008-05, Vol.120 (3-4), p.351-357

2008

Volltextzugriff (PDF)

Directly transmitted unbalanced chromosome abnormalities and euchromatic variants

Journal of Medical Genetics, 2005-08, Vol.42 (8), p.609-629

Barber, J C K

2005

Volltextzugriff (PDF)

Clinical feasibility of deep learning-based automatic head CBCT image segmentation and landmark detection in computer-aided surgical simulation for orthognathic surgery

International journal of oral and maxillofacial surgery, 2023-07, Vol.52 (7), p.793-800

2023

Volltextzugriff (PDF)

Is karyotyping couples experiencing recurrent miscarriage worth the cost?

BJOG : an international journal of obstetrics and gynaecology, 2010-06, Vol.117 (7), p.885-888

2010

Volltextzugriff (PDF)

A Novel Pseudo-Dicentric Variant of 16p11.2–q11.2 Contains Euchromatin from 16p11.2–p11.1 and Resembles Pathogenic Duplications of Proximal 16q

Cytogenetic and genome research, 2013-01, Vol.139 (1), p.59-64

2013

Volltextzugriff (PDF)

Copy number changes of the microcephalin 1 gene (MCPH1) in patients with autism spectrum disorders

Clinical genetics, 2009-10, Vol.76 (4), p.348-356

2009

Volltextzugriff (PDF)

Inherited Interstitial Duplications of Proximal 15q: Genotype-Phenotype Correlations

American journal of human genetics, 1997-12, Vol.61 (6), p.1342-1352

1997

Volltextzugriff (PDF)

Another Family with a Euchromatic Duplication Variant of 9q13-q21.1 Derived from Segmentally Duplicated Pericentromeric Euchromatin

Cytogenetic and genome research, 2013-01, Vol.141 (1), p.64-69

2013

Volltextzugriff (PDF)

Amplification of a pseudogene cassette underlies euchromatic variation of 16p at the cytogenetic level

Human genetics, 1999-03, Vol.104 (3), p.211-218

1999

Volltextzugriff (PDF)

Fertility, reproductive outcomes, and health of offspring, of patients treated for Hodgkin's disease: an investigation including chromosome examinations

British journal of cancer, 1996-07, Vol.74 (2), p.291-296

1996

Volltextzugriff (PDF)

Neurofibromatosis pseudogene amplification underlies euchromatic cytogenetic duplications and triplications of proximal 15q

Human genetics, 1998-11, Vol.103 (5), p.600-607

1998

Volltextzugriff (PDF)

A complex medical phenotype in a patient with triplication of 2q12.3 to 2q13 characterized with oligonucleotide array CGH

Cytogenetic and genome research, 2009-01, Vol.124 (2), p.179-186

2009

Volltextzugriff (PDF)

Reply to Dundar et. al. why a causal association between classical euchromatic variants of chromosome 9 and multiple miscarriages is unlikely

Genetic counseling, 2010-01, Vol.21 (4), p.469

Barber, J C K

2010

Volltextzugriff (PDF)

Unique marine Permian-Triassic boundary section from Western Australia

Australian journal of earth sciences, 2004-06, Vol.51 (3), p.423-430

2004

Volltextzugriff (PDF)

Further Evidence for an Imprinted Gene for Neonatal Diabetes Localised to Chromosome 6q22–q23

Human molecular genetics, 1996-08, Vol.5 (8), p.1117-1121

1996

Volltextzugriff (PDF)

t(8;21) myelodysplasia, an early presentation of M2 AML

British journal of haematology, 1995-04, Vol.89 (4), p.890-892

1995

Volltextzugriff (PDF)

Duplications of proximal 16q flanked by heterochromatin are not euchromatic variants and show no evidence of heterochromatic position effect

Cytogenetic and genome research, 2006-08, Vol.114 (3-4), p.351-358

2006

Volltextzugriff (PDF)

Ocular choristomas

Survey of Ophthalmology, 1989-03, Vol.33 (5), p.339-358

1989

Volltextzugriff (PDF)

Importance of microdeletions of chromosomal region 22q11 as a cause of selected malformations of the ventricular outflow tracts and aortic arch: A three-year prospective study

The Journal of pediatrics, 1996-07, Vol.129 (1), p.26-32

1996

Volltextzugriff (PDF)

Localisation of a gene for transient neonatal diabetes mellitus to an 18.72 cR3000 (∼5.4 Mb) interval on chromosome 6q

Journal of medical genetics, 1999-03, Vol.36 (3), p.192-196

1999

Volltextzugriff (PDF)

Plant-parasitic nematodes of New Zealand recorded by host association

Journal of nematology, 1997-12, Vol.29 (4), p.640-656

1997

Volltextzugriff (PDF)

RAPID IN SITU HARVESTING AND CYTOGENETIC ANALYSIS OF PERINATAL TISSUE SAMPLES

Prenatal diagnosis, 1996-07, Vol.16 (7), p.615-621

1996

Volltextzugriff (PDF)

Central venous catheter placement for intravenous digital subtraction angiography: an assessment of technical problems and success rate

British journal of radiology, 1989-07, Vol.62 (739), p.599-602

Barber, C J

1989

Volltextzugriff (PDF)

1 – 25 von 4.359

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(3.628)
Mit Volltextzugriff
(3.423)

Publikationsform

5 weitere anzeigen...

Weniger anzeigen...

Sprache

2 weitere anzeigen...

Weniger anzeigen...

Erscheinungsjahr

n.n

Thema

Science & Technology
(2.569)
Life Sciences & Biomedicine
(1.845)
Humans
(1.268)
Female
(726)
Biological And Medical Sciences
(723)
Male
(708)
Physical Sciences
(551)
Animals
(535)
Medical Sciences
(474)
Adult
(422)
Middle Aged
(390)
Technology
(360)
Physics
(342)
Aged
(307)
Fundamental And Applied Biological Sciences. Psychology
(292)
Biochemistry & Molecular Biology
(242)
Exact Sciences And Technology
(193)
Neurosciences & Neurology
(183)
Engineering
(177)
General & Internal Medicine
(176)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(18)
... seit 30 Tagen
(3)

Menü

Weitere Dienste

Einstellungen

Extensive Normal Copy Number Variation of a β-Defensin Antimicrobial-Gene Cluster

Transient neonatal diabetes: widening the understanding of the etiopathogenesis of diabetes

Repetitive DNA and chromosomal rearrangements: speciation-related events in plant genomes

Directly transmitted unbalanced chromosome abnormalities and euchromatic variants

Clinical feasibility of deep learning-based automatic head CBCT image segmentation and landmark detection in computer-aided surgical simulation for orthognathic surgery

Is karyotyping couples experiencing recurrent miscarriage worth the cost?

A Novel Pseudo-Dicentric Variant of 16p11.2–q11.2 Contains Euchromatin from 16p11.2–p11.1 and Resembles Pathogenic Duplications of Proximal 16q

Copy number changes of the microcephalin 1 gene (MCPH1) in patients with autism spectrum disorders

Inherited Interstitial Duplications of Proximal 15q: Genotype-Phenotype Correlations

Another Family with a Euchromatic Duplication Variant of 9q13-q21.1 Derived from Segmentally Duplicated Pericentromeric Euchromatin

Amplification of a pseudogene cassette underlies euchromatic variation of 16p at the cytogenetic level

Fertility, reproductive outcomes, and health of offspring, of patients treated for Hodgkin's disease: an investigation including chromosome examinations

Neurofibromatosis pseudogene amplification underlies euchromatic cytogenetic duplications and triplications of proximal 15q

A complex medical phenotype in a patient with triplication of 2q12.3 to 2q13 characterized with oligonucleotide array CGH

Reply to Dundar et. al. why a causal association between classical euchromatic variants of chromosome 9 and multiple miscarriages is unlikely

Unique marine Permian-Triassic boundary section from Western Australia

Further Evidence for an Imprinted Gene for Neonatal Diabetes Localised to Chromosome 6q22–q23

t(8;21) myelodysplasia, an early presentation of M2 AML

Duplications of proximal 16q flanked by heterochromatin are not euchromatic variants and show no evidence of heterochromatic position effect

Ocular choristomas

Importance of microdeletions of chromosomal region 22q11 as a cause of selected malformations of the ventricular outflow tracts and aortic arch: A three-year prospective study

Localisation of a gene for transient neonatal diabetes mellitus to an 18.72 cR3000 (∼5.4 Mb) interval on chromosome 6q

Plant-parasitic nematodes of New Zealand recorded by host association

RAPID IN SITU HARVESTING AND CYTOGENETIC ANALYSIS OF PERINATAL TISSUE SAMPLES

Central venous catheter placement for intravenous digital subtraction angiography: an assessment of technical problems and success rate

Suchergebnisse filtern