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...

P-12 Successful PGD for mitochondrial disease identifies positive selection for the m.8993 Tgt;G mutation

Reproductive biomedicine online, 2013-05, Vol.26, p.S31-S32

2013

Volltextzugriff (PDF)

O-6 Haplotype determination for PGD using flow sorted single chromosomes

Reproductive biomedicine online, 2013-05, Vol.26, p.S15-S15

2013

Volltextzugriff (PDF)

Preimplantation genetic testing for aneuploidy versus morphology as selection criteria for single frozen-thawed embryo transfer in good-prognosis patients: a multicenter randomized clinical trial

Fertility and sterility, 2019-12, Vol.112 (6), p.1071-1079.e7

2019

Volltextzugriff (PDF)

P-514 Unequal pronucleus size is indicative of higher rates of diploidy in 3PN blastocysts

Human reproduction (Oxford), 2024-07, Vol.39 (Supplement_1)

2024

Volltextzugriff (PDF)

4. PGT-M FOR DE NOVO MUTATIONS – HAPLOTYPE DETERMINATION USING MORPHOLOGICALLY POOR EMBRYOS

Reproductive biomedicine online, 2019-08, Vol.39, p.e15-e16

2019

Volltextzugriff (PDF)

Lymphedema distichiasis syndrome may be caused by FOXC2 promoter‐enhancer dissociation and disruption of a topological associated domain

American journal of medical genetics. Part A, 2021-01, Vol.185 (1), p.150-156

2021

Volltextzugriff (PDF)

Mosaicism in Human Embryos: What Do We Know?

Fertility & reproduction, 2022-09, Vol.4 (3n04), p.120-120

STOCK-MYER, Sharyn E.

2022

Volltextzugriff (PDF)

Genome-wide karyomapping accurately identifies the inheritance of single-gene defects in human preimplantation embryos in vitro

Genetics in medicine, 2014-11, Vol.16 (11), p.838-845

2014

Volltextzugriff (PDF)

290 : Does Extending the Time Interval Between hCG Trigger and Oocyte Retrieval from 36 to 37 Hours Affect the Rate of Euploid Blastocysts?

Fertility & reproduction, 2023-12, Vol.5 (4), p.380-381

2023

Volltextzugriff (PDF)

Is the Ploidy Status of the Embryo Impacted by Gonadotrophin Dose?

Fertility & reproduction, 2022-09, Vol.4 (3n04), p.172-172

2022

Volltextzugriff (PDF)

Is Cleavage Stage Multinucleation Indicative of Lower Pregnancy Potential in Euploid Blastocysts?

Fertility & reproduction, 2022-09, Vol.4 (3n04), p.188-188

2022

Volltextzugriff (PDF)

Three Mendelian disorders (chronic granulomatous disease, retinitis pigmentosa, ornithine transcarbamylase deficiency) in a young woman with an X chromosome deletion, del(X)(p11.4p21.1)

Molecular genetics and metabolism, 2010-03, Vol.99 (3), p.329-329

2010

Volltextzugriff (PDF)

A big step forward for PGT-M?

Reproductive biomedicine online, 2018-08, Vol.37 (2), p.126-127

2018

Volltextzugriff (PDF)

Preimplantation Genetic Testing for Aneuploidy Versus Morphology as Selection Criteria for Single Frozen-Thawed Embryo Transfer in Good-Prognosis Patients: A Multicenter Randomized Clinical Trial

Obstetrical & gynecological survey, 2020-04, Vol.75 (4), p.241-242

2020

Volltextzugriff (PDF)

77 Healthy baby girl born following PGD for the mitochondrial DNA mutation m.8993T>G

Mitochondrion, 2010-03, Vol.10 (2), p.222

2010

Volltextzugriff (PDF)

Three Mendelian disorders (chronic granulomatous disease, retinitis pigmentosa, ornithine transcarbamylase deficiency) in a young woman with an X chromosome deletion, del(X)(p11.4p21.1)

Molecular genetics and metabolism, 2010, Vol.99 (3), p.329-329

2010

Volltextzugriff (PDF)

1 – 16 von 16

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(15)
Mit Volltextzugriff
(15)

Publikationsform

Artikel
(15)
Berichte
(1)

Sprache

Englisch
(16)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

P-12 Successful PGD for mitochondrial disease identifies positive selection for the m.8993 Tgt;G mutation

O-6 Haplotype determination for PGD using flow sorted single chromosomes

Preimplantation genetic testing for aneuploidy versus morphology as selection criteria for single frozen-thawed embryo transfer in good-prognosis patients: a multicenter randomized clinical trial

P-514 Unequal pronucleus size is indicative of higher rates of diploidy in 3PN blastocysts

4. PGT-M FOR DE NOVO MUTATIONS – HAPLOTYPE DETERMINATION USING MORPHOLOGICALLY POOR EMBRYOS

Lymphedema distichiasis syndrome may be caused by FOXC2 promoter‐enhancer dissociation and disruption of a topological associated domain

Mosaicism in Human Embryos: What Do We Know?

Genome-wide karyomapping accurately identifies the inheritance of single-gene defects in human preimplantation embryos in vitro

290 : Does Extending the Time Interval Between hCG Trigger and Oocyte Retrieval from 36 to 37 Hours Affect the Rate of Euploid Blastocysts?

Is the Ploidy Status of the Embryo Impacted by Gonadotrophin Dose?

Is Cleavage Stage Multinucleation Indicative of Lower Pregnancy Potential in Euploid Blastocysts?

Three Mendelian disorders (chronic granulomatous disease, retinitis pigmentosa, ornithine transcarbamylase deficiency) in a young woman with an X chromosome deletion, del(X)(p11.4p21.1)

A big step forward for PGT-M?

Preimplantation Genetic Testing for Aneuploidy Versus Morphology as Selection Criteria for Single Frozen-Thawed Embryo Transfer in Good-Prognosis Patients: A Multicenter Randomized Clinical Trial

77 Healthy baby girl born following PGD for the mitochondrial DNA mutation m.8993T>G

Three Mendelian disorders (chronic granulomatous disease, retinitis pigmentosa, ornithine transcarbamylase deficiency) in a young woman with an X chromosome deletion, del(X)(p11.4p21.1)

Suchergebnisse filtern