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...

Aneuploidy in oocytes from women of advanced maternal age: analysis of the causal meiotic errors and impact on embryo development

Human reproduction (Oxford), 2023-12, Vol.38 (12), p.2526-2535

2023

Volltextzugriff (PDF)

Fabry Disease in Young Ischemic Stroke Patients in Northern Israel

Journal of stroke and cerebrovascular diseases, 2020-12, Vol.29 (12), p.105398-105398, Article 105398

2020

Volltextzugriff (PDF)

Polygenic embryo screening: four clinical considerations warrant further attention

Human reproduction (Oxford), 2022-06, Vol.37 (7), p.1375-1378

2022

Volltextzugriff (PDF)

Regional cerebral hyperperfusion and nitric oxide pathway dysregulation in Fabry disease : Reversal by enzyme replacement therapy

Circulation (New York, N.Y.), 2001-09, Vol.104 (13), p.1506-1512

2001

Volltextzugriff (PDF)

Ovarian reserve and PGD treatment outcome in women with myotonic dystrophy

Reproductive biomedicine online, 2014-07, Vol.29 (1), p.94-101

2014

Volltextzugriff (PDF)

Familial haplotyping and embryo analysis for Preimplantation Genetic Diagnosis (PGD) using DNA microarrays: a proof of principle study

Journal of assisted reproduction and genetics, 2013-12, Vol.30 (12), p.1595-1603

2013

Volltextzugriff (PDF)

Profile of endothelial and leukocyte activation in fabry patients

Annals of neurology, 2000-02, Vol.47 (2), p.229-233

2000

Volltextzugriff (PDF)

The neurogenetics of mucolipidosis type IV

Neurology, 2002-08, Vol.59 (3), p.306-313

2002

Volltextzugriff (PDF)

Identification of fifteen novel mutations and genotype-phenotype relationship in Fabry disease

Clinical genetics, 2001-07, Vol.60 (1), p.46-51

2001

Volltextzugriff (PDF)

Single-sperm analysis for haplotype construction of de-novo paternal mutations: application to PGD for neurofibromatosis type 1

Human reproduction (Oxford), 2006-08, Vol.21 (8), p.2047-2051

2006

Volltextzugriff (PDF)

O-22 Embryo biopsy for PGD has no significant impact on neonatal outcome

Reproductive biomedicine online, 2013-05, Vol.26, p.S22-S22

2013

Volltextzugriff (PDF)

P-2 Overcoming limitations of single cell analysis in duplicated and GC-rich genomic regions using multiple displacement amplification for preimplantation genetic diagnosis (PGD)

Reproductive biomedicine online, 2013-05, Vol.26, p.S27-S28

2013

Volltextzugriff (PDF)

P2 Instant familial haplotyping in conjunction with embryo analysis in preimplantation genetic diagnosis (PGD) using DNA microarrays

Reproductive biomedicine online, 2012-05, Vol.24, p.S45-S45

2012

Volltextzugriff (PDF)

Correlation between interleukin-6 promoter and C-reactive protein (CRP) polymorphisms and CRP levels with the Mainz Severity Score Index for Fabry disease

Journal of inherited metabolic disease, 2008-02, Vol.31 (1), p.117-123

2008

Volltextzugriff (PDF)

Successful polar body-based preimplantation genetic diagnosis for achondroplasia

Reproductive biomedicine online, 2008, Vol.16 (2), p.276-282

2008

Volltextzugriff (PDF)

Prostanoid DP receptor (PTGDR) variants in mothers with post-coital associated preterm births: preliminary observations

Journal of perinatology, 2010-01, Vol.30 (1), p.33-37

2010

Volltextzugriff (PDF)

O-307 Aneuploidy in oocytes of women of advanced maternal age: impact on embryo development and evidence for a novel mechanism of meiotic error

Human reproduction (Oxford), 2023-06, Vol.38 (Supplement_1)

2023

Volltextzugriff (PDF)

O1 Preimplantation Genetic Diagnosis (PGD) for germline mosaicism

Reproductive biomedicine online, 2010, Vol.20, p.S15-S15

2010

Volltextzugriff (PDF)

Aneuploidy in Oocytes From Women of Advanced Maternal Age: Analysis of the Causal Meiotic Errors and Impact on Embryo Development

Obstetrical & gynecological survey, 2024-03, Vol.79 (3), p.164-165

2024

Volltextzugriff (PDF)

Uveitis and Fabry disease

Eye (London), 2007-03, Vol.21 (3), p.448-448

2007

Volltextzugriff (PDF)

Advantages of multiple markers and polar body analysis in preimplantation genetic diagnosis for Alagille disease

Prenatal diagnosis, 2007-04, Vol.27 (4), p.317-321

2007

Volltextzugriff (PDF)

50. ASSESSMENT OF MICROBIAL CONTAMINATION TO ELIMINATE ARTIFACTS IN SEQUENCING-BASED PGT-A/PGT-SR

Reproductive biomedicine online, 2019-08, Vol.39, p.e57-e57

2019

Volltextzugriff (PDF)

49. Molecular PGT-M for VUS in the genomic era: to do or not to do?

Reproductive biomedicine online, 2019-08, Vol.39, p.e56-e57

2019

Volltextzugriff (PDF)

O8 Preimplantation genetic diagnosis (PGD) for monogenic disorders. When blastomere analysis may be impossible

Reproductive biomedicine online, 2010, Vol.20, p.S17-S17

2010

Volltextzugriff (PDF)

Enzyme replacement therapy with agalsidase alfa in patients with Fabry's disease: an analysis of registry data

The Lancet (British edition), 2009-12, Vol.374 (9706), p.1986-1996

2009

Volltextzugriff (PDF)

1 – 25 von 70

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(66)
Mit Volltextzugriff
(56)

Publikationsform

Artikel
(69)
Tagungsberichte
(1)

Sprache

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Aneuploidy in oocytes from women of advanced maternal age: analysis of the causal meiotic errors and impact on embryo development

Fabry Disease in Young Ischemic Stroke Patients in Northern Israel

Polygenic embryo screening: four clinical considerations warrant further attention

Regional cerebral hyperperfusion and nitric oxide pathway dysregulation in Fabry disease : Reversal by enzyme replacement therapy

Ovarian reserve and PGD treatment outcome in women with myotonic dystrophy

Familial haplotyping and embryo analysis for Preimplantation Genetic Diagnosis (PGD) using DNA microarrays: a proof of principle study

Profile of endothelial and leukocyte activation in fabry patients

The neurogenetics of mucolipidosis type IV

Identification of fifteen novel mutations and genotype-phenotype relationship in Fabry disease

Single-sperm analysis for haplotype construction of de-novo paternal mutations: application to PGD for neurofibromatosis type 1

O-22 Embryo biopsy for PGD has no significant impact on neonatal outcome

P-2 Overcoming limitations of single cell analysis in duplicated and GC-rich genomic regions using multiple displacement amplification for preimplantation genetic diagnosis (PGD)

P2 Instant familial haplotyping in conjunction with embryo analysis in preimplantation genetic diagnosis (PGD) using DNA microarrays

Correlation between interleukin-6 promoter and C-reactive protein (CRP) polymorphisms and CRP levels with the Mainz Severity Score Index for Fabry disease

Successful polar body-based preimplantation genetic diagnosis for achondroplasia

Prostanoid DP receptor (PTGDR) variants in mothers with post-coital associated preterm births: preliminary observations

O-307 Aneuploidy in oocytes of women of advanced maternal age: impact on embryo development and evidence for a novel mechanism of meiotic error

O1 Preimplantation Genetic Diagnosis (PGD) for germline mosaicism

Aneuploidy in Oocytes From Women of Advanced Maternal Age: Analysis of the Causal Meiotic Errors and Impact on Embryo Development

Uveitis and Fabry disease

Advantages of multiple markers and polar body analysis in preimplantation genetic diagnosis for Alagille disease

50. ASSESSMENT OF MICROBIAL CONTAMINATION TO ELIMINATE ARTIFACTS IN SEQUENCING-BASED PGT-A/PGT-SR

49. Molecular PGT-M for VUS in the genomic era: to do or not to do?

O8 Preimplantation genetic diagnosis (PGD) for monogenic disorders. When blastomere analysis may be impossible

Enzyme replacement therapy with agalsidase alfa in patients with Fabry's disease: an analysis of registry data

Suchergebnisse filtern