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...

Complex biology of constitutional ring chromosomes structure and (in)stability revealed by somatic cell reprogramming

Scientific reports, 2021-02, Vol.11 (1), p.4325-4325, Article 4325

2021

Volltextzugriff (PDF)

Concomitant CNVs in healthy carriers with 7q31.1 microdeletions may suppress intellectual disability and autism spectrum disorders phenotype

European psychiatry, 2022-06, Vol.65 (S1), p.S382-S382

2022

Volltextzugriff (PDF)

Combined whole exome sequencing and chromosomal microarray analysis improve clinical interpretation of genomic variants in patients with intellectual disability

European psychiatry, 2023-03, Vol.66 (S1), p.S887-S887

2023

Volltextzugriff (PDF)

Identification of candidate genes of intellectual disability by single-gene deletions/amplifications mapping using chromosomal microarray analysis

European psychiatry, 2022-06, Vol.65 (S1), p.S382-S382

2022

Volltextzugriff (PDF)

A case report of Pallister-Killian syndrome with an unusual mosaic supernumerary marker chromosome 12 with interstitial 12p13.1-p12.1 duplication

Frontiers in genetics, 2024-03, Vol.15, p.1331066-1331066

2024

Volltextzugriff (PDF)

Building Life-Cycle Management. Information Systems and Technologies: Selected Papers

1, 2022

Volltextzugriff (PDF)

Diagnostic yield of chromosomal microarray and trio whole exome sequencing in congenital brain anomalies

European psychiatry, 2023-03, Vol.66 (S1), p.S887-S887

2023

Volltextzugriff (PDF)

Identification of differentially methylated genes in first-trimester placentas with trisomy 16

Scientific reports, 2022-01, Vol.12 (1), p.1166-1166, Article 1166

2022

Volltextzugriff (PDF)

Generation of iPS cell line (ICGi040-A) from skin fibroblasts of a patient with ring small supernumerary marker chromosome 4

Stem cell research, 2022-05, Vol.61, p.102740-102740, Article 102740

2022

Volltextzugriff (PDF)

Integration of blockchain and artificial intelligence as a mechanism for modernisation of various economic sectors

Вестник университета, 2024-06 (5), p.54-67

2024

Volltextzugriff (PDF)

Generation of iPSC line ICGi024-A from human skin fibroblasts of a patient with ring chromosome 18

Stem cell research, 2020-12, Vol.49, p.102076-102076, Article 102076

2020

Volltextzugriff (PDF)

Establishment of an induced pluripotent stem cell line (ICGi025-A) from fibroblasts of a patient with 46,XY,r(8)/45,XY,–8 mosaicism

Stem cell research, 2020-12, Vol.49, p.102024-102024, Article 102024

2020

Volltextzugriff (PDF)

Generation of Induced Pluripotent Stem Cell Line iTAF15Xsk4 from Fibroblasts of a Patient with Microdeletion at Xq24

Russian journal of developmental biology, 2023-12, Vol.54 (6), p.358-364

2023

Volltextzugriff (PDF)

Induced pluripotent stem cell line, IMGTi003-A, derived from skin fibroblasts of an intellectually disabled patient with ring chromosome 13

Stem cell research, 2018-12, Vol.33, p.260-264

2018

Volltextzugriff (PDF)

Generation of the induced pluripotent stem cell line, ICAGi002-A, from unaffected carrier megabase scaled duplication involving the CNTN6 gene

Stem cell research, 2019-10, Vol.40, p.101556-101556, Article 101556

2019

Volltextzugriff (PDF)

Prenatal Diagnosis of Small Supernumerary Marker Chromosome 10 by Array-Based Comparative Genomic Hybridization and Microdissected Chromosome Sequencing

Biomedicines, 2021-08, Vol.9 (8), p.1030

2021

Volltextzugriff (PDF)

Generation of four iPSC lines from two siblings with a microdeletion at the CNTN6 gene and intellectual disability

Stem cell research, 2019-12, Vol.41, p.101591-101591, Article 101591

2019

Volltextzugriff (PDF)

Generation of two iPSC lines (IMGTi001-A and IMGTi001-B) from human skin fibroblasts with ring chromosome 22

Stem cell research, 2018-08, Vol.31, p.244-248

2018

Volltextzugriff (PDF)

Non-fungible token: a promising digital tool for business

Вестник университета, 2022-05 (3), p.44-51

2022

Volltextzugriff (PDF)

Analysis of the use of the electronic document management system in federal executive authorities

Вестник университета, 2021-09 (7), p.43-51

2021

Volltextzugriff (PDF)

Induced pluripotent stem cell line, ICAGi001-A, derived from human skin fibroblasts of a patient with 2p25.3 deletion and 2p25.3-p23.3 inverted duplication

Stem cell research, 2019-01, Vol.34, p.101377-101377, Article 101377

2019

Volltextzugriff (PDF)

Genomic architecture of human chromosomal diseases

Russian journal of genetics, 2016-05, Vol.52 (5), p.447-462

2016

Volltextzugriff (PDF)

Compound phenotype in a girl with r(22), concomitant microdeletion 22q13.32-q13.33 and mosaic monosomy 22

Molecular cytogenetics, 2018-04, Vol.11 (1), p.26-26, Article 26

2018

Volltextzugriff (PDF)

Estimation of association of CNTN6 copy number variation with idiopathic intellectual disability

Russian journal of genetics, 2016-09, Vol.52 (9), p.1004-1006

2016

Volltextzugriff (PDF)

Runs of homozygosity in spontaneous abortions from families with recurrent pregnancy loss

Vavilovskiĭ zhurnal genetiki i selekt͡s︡ii, 2019-01, Vol.23 (2), p.244-249

2019

Volltextzugriff (PDF)

1 – 25 von 374

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(281)
Mit Volltextzugriff
(240)

Publikationsform

Sprache

Erscheinungsjahr

n.n

Thema

Science & Technology
(96)
Life Sciences & Biomedicine
(51)
Humans
(30)
Technology
(30)
Physical Sciences
(28)
Osteoarthritis
(26)
Female
(23)
Genetics & Heredity
(23)
Physics
(19)
Biomedical And Life Sciences
(18)
Materials Science
(18)
Engineering
(16)
Materials Science, Multidisciplinary
(16)
Human Genetics
(15)
Adult
(14)
Chemistry
(14)
Male
(14)
Cell Biology
(13)
Chemistry, Physical
(13)
Biomedicine
(12)

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(5)

Menü

Weitere Dienste

Einstellungen

Complex biology of constitutional ring chromosomes structure and (in)stability revealed by somatic cell reprogramming

Concomitant CNVs in healthy carriers with 7q31.1 microdeletions may suppress intellectual disability and autism spectrum disorders phenotype

Combined whole exome sequencing and chromosomal microarray analysis improve clinical interpretation of genomic variants in patients with intellectual disability

Identification of candidate genes of intellectual disability by single-gene deletions/amplifications mapping using chromosomal microarray analysis

A case report of Pallister-Killian syndrome with an unusual mosaic supernumerary marker chromosome 12 with interstitial 12p13.1-p12.1 duplication

Building Life-Cycle Management. Information Systems and Technologies: Selected Papers

Diagnostic yield of chromosomal microarray and trio whole exome sequencing in congenital brain anomalies

Identification of differentially methylated genes in first-trimester placentas with trisomy 16

Generation of iPS cell line (ICGi040-A) from skin fibroblasts of a patient with ring small supernumerary marker chromosome 4

Integration of blockchain and artificial intelligence as a mechanism for modernisation of various economic sectors

Generation of iPSC line ICGi024-A from human skin fibroblasts of a patient with ring chromosome 18

Establishment of an induced pluripotent stem cell line (ICGi025-A) from fibroblasts of a patient with 46,XY,r(8)/45,XY,–8 mosaicism

Generation of Induced Pluripotent Stem Cell Line iTAF15Xsk4 from Fibroblasts of a Patient with Microdeletion at Xq24

Induced pluripotent stem cell line, IMGTi003-A, derived from skin fibroblasts of an intellectually disabled patient with ring chromosome 13

Generation of the induced pluripotent stem cell line, ICAGi002-A, from unaffected carrier megabase scaled duplication involving the CNTN6 gene

Prenatal Diagnosis of Small Supernumerary Marker Chromosome 10 by Array-Based Comparative Genomic Hybridization and Microdissected Chromosome Sequencing

Generation of four iPSC lines from two siblings with a microdeletion at the CNTN6 gene and intellectual disability

Generation of two iPSC lines (IMGTi001-A and IMGTi001-B) from human skin fibroblasts with ring chromosome 22

Non-fungible token: a promising digital tool for business

Analysis of the use of the electronic document management system in federal executive authorities

Induced pluripotent stem cell line, ICAGi001-A, derived from human skin fibroblasts of a patient with 2p25.3 deletion and 2p25.3-p23.3 inverted duplication

Genomic architecture of human chromosomal diseases

Compound phenotype in a girl with r(22), concomitant microdeletion 22q13.32-q13.33 and mosaic monosomy 22

Estimation of association of CNTN6 copy number variation with idiopathic intellectual disability

Runs of homozygosity in spontaneous abortions from families with recurrent pregnancy loss

Suchergebnisse filtern