UB Paderborn / Katalog / Suche / in CDI

Prenatal diagnosis of Kagami‐Ogata syndrome

Journal of clinical ultrasound, 2021-06, Vol.49 (5), p.498-501

2021

Volltextzugriff (PDF)

A New Stepwise Molecular Work-Up After Chorionic Villi Sampling in Women With an Early Pregnancy Loss

Frontiers in genetics, 2021-01, Vol.11, p.561720-561720

2021

Volltextzugriff (PDF)

Do FETO CDH survivors need the same follow-up program as non-FETO patients?

European journal of pediatrics, 2023-07, Vol.182 (7), p.3243-3255

2023

Volltextzugriff (PDF)

New Gestational Phase–Specific Cutoff Values for the Use of the Soluble fms-Like Tyrosine Kinase-1/Placental Growth Factor Ratio as a Diagnostic Test for Preeclampsia

Hypertension (Dallas, Tex. 1979), 2014-02, Vol.63 (2), p.346-352

2014

Volltextzugriff (PDF)

Perinatal outcome after selective termination in dichorionic twins discordant for congenital anomalies

Acta obstetricia et gynecologica Scandinavica, 2021-11, Vol.100 (11), p.2029-2035

2021

Volltextzugriff (PDF)

Genomic Microarray in Fetuses with Early Growth Restriction: A Multicenter Study

Fetal diagnosis and therapy, 2017-10, Vol.42 (3), p.174-180

2017

Volltextzugriff (PDF)

Heterotrisomy recurrence risk: a practical maternal age-dependent approach for excess trisomy 21 risk calculation after a previous autosomal trisomy

The journal of maternal-fetal & neonatal medicine, 2017-07, Vol.30 (13), p.1613-1615

2017

Volltextzugriff (PDF)

Next-Generation Sequencing Gene Panels and “Solo” Clinical Exome Sequencing Applied in Structurally Abnormal Fetuses

Fetal diagnosis and therapy, 2021-12, Vol.48 (10), p.746-756

2021

Volltextzugriff (PDF)

Effectiveness of ovarian age as the background risk for aneuploidy screening in an unselected pregnant population

Reproductive biomedicine online, 2016-10, Vol.33 (4), p.500-505

2016

Volltextzugriff (PDF)

European reference network for rare inherited congenital anomalies (ERNICA) evidence based guideline on the management of gastroschisis

Orphanet journal of rare diseases, 2024-02, Vol.19 (1), p.60-16, Article 60

2024

Volltextzugriff (PDF)

Role of 3‐Dimensional Power Doppler Sonography in Differentiating Pregnant Women With Threatened Preterm Labor From Those With an Asymptomatic Short Cervix

Journal of ultrasound in medicine, 2014-04, Vol.33 (4), p.673-679

2014

Volltextzugriff (PDF)

Genomic Microarray in Fetuses With Early Growth Restriction: A Multicenter Study

Obstetrical & gynecological survey, 2018-02, Vol.73 (2), p.73-74

2018

Volltextzugriff (PDF)

310: Prediction of neonatal respiratory morbidity by quantitative ultrasound lung texture analysis: a multicenter study

American journal of obstetrics and gynecology, 2017-01, Vol.216 (1), p.S190-S190

2017

Volltextzugriff (PDF)

Cord blood collection for banking and the risk of maternal hemorrhage

Acta obstetricia et gynecologica Scandinavica, 2011-09, Vol.90 (9), p.1043-1045

2011

Volltextzugriff (PDF)

Prediction of neonatal respiratory morbidity by quantitative ultrasound lung texture analysis: a multicenter study

American journal of obstetrics and gynecology, 2017-08, Vol.217 (2), p.196.e1-196.e14

2017

Volltextzugriff (PDF)

Control de calidad en el cribado prenatal de aneuploidías

Diagnóstico prenatal, 2012-01, Vol.23 (1), p.15-24

2012

Volltextzugriff (PDF)

Chromosome microarray analysis should be offered to all invasive prenatal diagnostic testing following a normal rapid aneuploidy test result

Clinical genetics, 2020-10, Vol.98 (4), p.379-383

2020

Volltextzugriff (PDF)

Analysis of Quality of Nuchal Translucency Measurements

Donald School journal of ultrasound in obstetrics and gynecology, 2011-06, Vol.5 (2), p.127-132

2011

Volltextzugriff (PDF)

The use of biochemical markers in prenatal diagnosis of intrauterine growth retardation: insulin-like growth factor I, Leptin, and alpha-fetoprotein

European journal of obstetrics & gynecology and reproductive biology, 2005-05, Vol.120 (1), p.27-32

2005

Volltextzugriff (PDF)

Crown-rump length audit plots with the use of operator-specific PAPP-A and [beta]-hCG median MoM

Prenatal diagnosis, 2017-03, Vol.37 (3), p.229

2017

Volltextzugriff (PDF)

Crown‐rump length audit plots with the use of operator‐specific PAPP‐A and β‐hCG median MoM

Prenatal diagnosis, 2017-03, Vol.37 (3), p.229-234

2017

Volltextzugriff (PDF)

Preimplantation genetic testing for a chr14q32 microdeletion in a family with Kagami-Ogata syndrome and Temple syndrome

Journal of medical genetics, 2022-03, Vol.59 (3), p.253

2022

Volltextzugriff (PDF)

Cumulative sum plots and retrospective parameters in first-trimester ductus venosus quality assurance

Prenatal diagnosis, 2013-04, Vol.33 (4), p.384-390

2013

Volltextzugriff (PDF)

Updated Reference Ranges for the Ductus Venosus Pulsatility Index at 11–13 Weeks

Fetal diagnosis and therapy, 2012-01, Vol.32 (4), p.271-276

2012

Volltextzugriff (PDF)

Heterotrisomy recurrence risk: a practical maternal age-dependent approach for excess trisomy 21 risk calculation after a previous autosomal trisomy

The Journal of Maternal-Fetal & Neonatal Medicine, 2017, Vol.30 (13), p.1613-1615

2017

Volltextzugriff (PDF)

Menü

Weitere Dienste

Einstellungen

Prenatal diagnosis of Kagami‐Ogata syndrome

A New Stepwise Molecular Work-Up After Chorionic Villi Sampling in Women With an Early Pregnancy Loss

Do FETO CDH survivors need the same follow-up program as non-FETO patients?

New Gestational Phase–Specific Cutoff Values for the Use of the Soluble fms-Like Tyrosine Kinase-1/Placental Growth Factor Ratio as a Diagnostic Test for Preeclampsia

Perinatal outcome after selective termination in dichorionic twins discordant for congenital anomalies

Genomic Microarray in Fetuses with Early Growth Restriction: A Multicenter Study

Heterotrisomy recurrence risk: a practical maternal age-dependent approach for excess trisomy 21 risk calculation after a previous autosomal trisomy

Next-Generation Sequencing Gene Panels and “Solo” Clinical Exome Sequencing Applied in Structurally Abnormal Fetuses

Effectiveness of ovarian age as the background risk for aneuploidy screening in an unselected pregnant population

European reference network for rare inherited congenital anomalies (ERNICA) evidence based guideline on the management of gastroschisis

Role of 3‐Dimensional Power Doppler Sonography in Differentiating Pregnant Women With Threatened Preterm Labor From Those With an Asymptomatic Short Cervix

Genomic Microarray in Fetuses With Early Growth Restriction: A Multicenter Study

310: Prediction of neonatal respiratory morbidity by quantitative ultrasound lung texture analysis: a multicenter study

Cord blood collection for banking and the risk of maternal hemorrhage

Prediction of neonatal respiratory morbidity by quantitative ultrasound lung texture analysis: a multicenter study

Control de calidad en el cribado prenatal de aneuploidías

Chromosome microarray analysis should be offered to all invasive prenatal diagnostic testing following a normal rapid aneuploidy test result

Analysis of Quality of Nuchal Translucency Measurements

The use of biochemical markers in prenatal diagnosis of intrauterine growth retardation: insulin-like growth factor I, Leptin, and alpha-fetoprotein

Crown-rump length audit plots with the use of operator-specific PAPP-A and [beta]-hCG median MoM

Crown‐rump length audit plots with the use of operator‐specific PAPP‐A and β‐hCG median MoM

Preimplantation genetic testing for a chr14q32 microdeletion in a family with Kagami-Ogata syndrome and Temple syndrome

Cumulative sum plots and retrospective parameters in first-trimester ductus venosus quality assurance

Updated Reference Ranges for the Ductus Venosus Pulsatility Index at 11–13 Weeks

Heterotrisomy recurrence risk: a practical maternal age-dependent approach for excess trisomy 21 risk calculation after a previous autosomal trisomy

Suchergebnisse filtern