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...

Non‐invasive prenatal testing for trisomy 21: a cross‐sectional survey of service users' views and likely uptake

BJOG : an international journal of obstetrics and gynaecology, 2014-04, Vol.121 (5), p.582-594

2014

Volltextzugriff (PDF)

Factors affecting uptake of postmortem examination in the prenatal, perinatal and paediatric setting

BJOG : an international journal of obstetrics and gynaecology, 2018-01, Vol.125 (2), p.172-181

2018

Volltextzugriff (PDF)

Evidence to Support the Clinical Utility of Prenatal Exome Sequencing in Evaluation of the Fetus with Congenital Anomalies: Scientific Impact Paper No. 64 [February] 2021

BJOG : an international journal of obstetrics and gynaecology, 2021-08, Vol.128 (9), p.e39-e50

2021

Volltextzugriff (PDF)

Non-invasive prenatal diagnosis for single gene disorders: experience of patients

Clinical genetics, 2014-04, Vol.85 (4), p.336-342

2014

Volltextzugriff (PDF)

Non-invasive prenatal determination of fetal sex: translating research into clinical practice

Clinical genetics, 2011-07, Vol.80 (1), p.68-75

2011

Volltextzugriff (PDF)

Availability of less invasive prenatal, perinatal and paediatric autopsy will improve uptake rates: a mixed‐methods study with bereaved parents

BJOG : an international journal of obstetrics and gynaecology, 2019-05, Vol.126 (6), p.745-753

2019

Volltextzugriff (PDF)

Evidence to Support the Clinical Utility of Prenatal Exome Sequencing in Evaluation of the Fetus with Congenital Anomalies

BJOG : an international journal of obstetrics and gynaecology, 2021-08, Vol.128 (9), p.e39-e50

2021

Volltextzugriff (PDF)

P30.03: Ventriculomegaly at 11–14 weeks: diagnostic criteria and outcome

Ultrasound in obstetrics & gynecology, 2016-09, Vol.48 (S1), p.267-267

2016

Volltextzugriff (PDF)

Factors that impact on women's decision‐making around prenatal genomic tests: An international discrete choice survey

Prenatal diagnosis, 2022-06, Vol.42 (7), p.934-946

2022

Volltextzugriff (PDF)

Stakeholder views and attitudes towards prenatal and postnatal transplantation of fetal mesenchymal stem cells to treat Osteogenesis Imperfecta

European journal of human genetics : EJHG, 2019-08, Vol.27 (8), p.1244-1253

2019

Volltextzugriff (PDF)

BOOSTB4 – eine klinische Studie zur prä- und/oder postnatalen Stammzelltherapie zur Behandlung der Osteogenesis imperfecta

Geburtshilfe und Frauenheilkunde, 2016, Vol.76 (10)

2016

Volltextzugriff (PDF)

In case you missed it: The Prenatal Diagnosis editors bring you the most significant advances of 2019

Prenatal diagnosis, 2020-02, Vol.40 (3), p.287-293

2020

Volltextzugriff (PDF)

Living with osteogenesis imperfecta: A qualitative study exploring experiences and psychosocial impact from the perspective of patients, parents and professionals

Disability and health journal, 2022-01, Vol.15 (1), p.101168-101168, Article 101168

2022

Volltextzugriff (PDF)

OP08.09: Rapid whole exome sequencing for the prenatal diagnosis sonographic abnormalities

Ultrasound in obstetrics & gynecology, 2016-09, Vol.48 (S1), p.77-77

2016

Volltextzugriff (PDF)

OC06.02: Expanding analysis of cell‐free DNA to deliver safe, accurate, speedy diagnosis of skeletal dysplasias and other monogenic disorders

Ultrasound in obstetrics & gynecology, 2016-09, Vol.48 (S1), p.10-10

2016

Volltextzugriff (PDF)

Evaluation of preferences of women and healthcare professionals in Singapore for implementation of noninvasive prenatal testing for Down syndrome

Singapore medical journal, 2017-06, Vol.58 (6), p.298-310

2017

Volltextzugriff (PDF)

Authors' reply: Noninvasive prenatal testing for trisomy 21: when counselling is needed before responding to a survey

BJOG : an international journal of obstetrics and gynaecology, 2014-10, Vol.121 (11), p.1444-1444

2014

Volltextzugriff (PDF)

EP21.04: BOOSTB4: a clinical study to determine safety and efficacy of pre‐ and/or postnatal stem cell transplantation for treatment of osteogenesis imperfecta

Ultrasound in obstetrics & gynecology, 2016-09, Vol.48 (S1), p.356-356

2016

Volltextzugriff (PDF)

Stakeholder views towards prenatal and postnatal fetal mesenchymal stem cell infusions for osteogenesis imperfecta

EUROPEAN JOURNAL OF HUMAN GENETICS, 2019, Vol.27, p.707

2019

Volltextzugriff (PDF)

Fetal nuchal translucency scan and early prenatal diagnosis of chromosomal abnormalities by rapid aneuploidy screening: observational study

BMJ, 2006-02, Vol.332 (7539), p.452-455

2006

Volltextzugriff (PDF)

Women and health care professionals' preferences for Down's Syndrome screening tests: a conjoint analysis study

BJOG : an international journal of obstetrics and gynaecology, 2004-08, Vol.111 (8), p.775-779

2004

Volltextzugriff (PDF)

Prenatal gender determination and the diagnosis of genital anomalies

BJU international, 2004-05, Vol.93 (s3), p.12-19

2004

Volltextzugriff (PDF)

Fetal cardiac anomalies and genetic syndromes

Prenatal diagnosis, 2004-12, Vol.24 (13), p.1104-1115

2004

Volltextzugriff (PDF)

Ultrasound screening for fetal abnormalities

Prenatal diagnosis, 1995-12, Vol.15 (13), p.1241-1257

Chitty, Lyn S.

1995

Volltextzugriff (PDF)

1 – 25 von 59

Suche als RSS-Feed

Aktive Filter

Zeitschrift / SerieArchives Of Disease In Childhood. Fetal And Neonatal Edition

ThemaProspective Studies

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(57)
Mit Volltextzugriff
(53)

Publikationsform

Artikel
(57)
Tagungsberichte
(2)

Sprache

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Non‐invasive prenatal testing for trisomy 21: a cross‐sectional survey of service users' views and likely uptake

Factors affecting uptake of postmortem examination in the prenatal, perinatal and paediatric setting

Evidence to Support the Clinical Utility of Prenatal Exome Sequencing in Evaluation of the Fetus with Congenital Anomalies: Scientific Impact Paper No. 64 [February] 2021

Non-invasive prenatal diagnosis for single gene disorders: experience of patients

Non-invasive prenatal determination of fetal sex: translating research into clinical practice

Availability of less invasive prenatal, perinatal and paediatric autopsy will improve uptake rates: a mixed‐methods study with bereaved parents

Evidence to Support the Clinical Utility of Prenatal Exome Sequencing in Evaluation of the Fetus with Congenital Anomalies

P30.03: Ventriculomegaly at 11–14 weeks: diagnostic criteria and outcome

Factors that impact on women's decision‐making around prenatal genomic tests: An international discrete choice survey

Stakeholder views and attitudes towards prenatal and postnatal transplantation of fetal mesenchymal stem cells to treat Osteogenesis Imperfecta

BOOSTB4 – eine klinische Studie zur prä- und/oder postnatalen Stammzelltherapie zur Behandlung der Osteogenesis imperfecta

An exploratory open-label multicentre phase I/II trial evaluating the safety and efficacy of postnatal or prenatal and postnatal administration of allogeneic expanded fetal mesenchymal stem cells for the treatment of severe osteogenesis imperfecta in infants and fetuses: the BOOSTB4 trial protocol

In case you missed it: The Prenatal Diagnosis editors bring you the most significant advances of 2019

Living with osteogenesis imperfecta: A qualitative study exploring experiences and psychosocial impact from the perspective of patients, parents and professionals

OP08.09: Rapid whole exome sequencing for the prenatal diagnosis sonographic abnormalities

OC06.02: Expanding analysis of cell‐free DNA to deliver safe, accurate, speedy diagnosis of skeletal dysplasias and other monogenic disorders

Evaluation of preferences of women and healthcare professionals in Singapore for implementation of noninvasive prenatal testing for Down syndrome

Authors' reply: Noninvasive prenatal testing for trisomy 21: when counselling is needed before responding to a survey

EP21.04: BOOSTB4: a clinical study to determine safety and efficacy of pre‐ and/or postnatal stem cell transplantation for treatment of osteogenesis imperfecta

Stakeholder views towards prenatal and postnatal fetal mesenchymal stem cell infusions for osteogenesis imperfecta

Fetal nuchal translucency scan and early prenatal diagnosis of chromosomal abnormalities by rapid aneuploidy screening: observational study

Women and health care professionals' preferences for Down's Syndrome screening tests: a conjoint analysis study

Prenatal gender determination and the diagnosis of genital anomalies

Fetal cardiac anomalies and genetic syndromes

Ultrasound screening for fetal abnormalities

Aktive Filter

Suchergebnisse filtern