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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

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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

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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

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

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

2014

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

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

2011

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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

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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

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

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

2016

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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

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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

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

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

2016

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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

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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

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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

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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

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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

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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

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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

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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

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1.1 Non-Invasive Prenatal Testing Using Cell Free Fetal DNA in Maternal Plasma: An Aid to Prenatal Sonographic Diagnosis: Abstract 1.1 Table

Archives of disease in childhood. Fetal and neonatal edition, 2013-04, Vol.98 (Suppl 1), p.A1-A1

2013

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1.1 Non-Invasive Prenatal Testing Using Cell Free Fetal DNA in Maternal Plasma: An Aid to Prenatal Sonographic Diagnosis

Archives of disease in childhood. Fetal and neonatal edition, 2013-04, Vol.98 (Suppl 1), p.A1

2013

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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

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Abnormalities of the fetal lower limb: prenatal diagnosis and prognosis

Archives of disease in childhood. Fetal and neonatal edition, 2010-06, Vol.95 (Suppl 1), p.Fa25-Fa25

2010

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Prenatal gender determination and the diagnosis of genital anomalies

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

2004

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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

1.1 Non-Invasive Prenatal Testing Using Cell Free Fetal DNA in Maternal Plasma: An Aid to Prenatal Sonographic Diagnosis: Abstract 1.1 Table

1.1 Non-Invasive Prenatal Testing Using Cell Free Fetal DNA in Maternal Plasma: An Aid to Prenatal Sonographic Diagnosis

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

Abnormalities of the fetal lower limb: prenatal diagnosis and prognosis

Prenatal gender determination and the diagnosis of genital anomalies

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