Lista de obras - Angela N Barrett - Dominio Público Uruguay

Application of real-time PCR of sex-independent insertion-deletion polymorphisms to determine fetal sex using cell-free fetal DNA from maternal plasma

artículo científico publicado en 2015

Authors' Reply: The assessment of combined first trimester screening in women of advanced maternal age in an Asian cohort.

artículo científico publicado en 2015

Biology of human primitive erythroblasts for application in noninvasive prenatal diagnosis

artículo científico publicado en 2018

Blood Chimerism in Dizygotic Monochorionic Twins During 5 Years Observation

artículo científico publicado en 2017

Breast cancer associated transcriptional repressor PLU-1/JARID1B interacts directly with histone deacetylases

artículo científico publicado en 2007

Challenges in non-invasive prenatal screening for sub-chromosomal copy number variations using cell-free DNA.

artículo científico publicado en 2017

Detection of aneuploidy from single fetal nucleated red blood cells using whole genome sequencing

artículo científico publicado en 2014

Developing noninvasive diagnosis for single-gene disorders: the role of digital PCR.

artículo científico publicado en 2014

Digital PCR analysis of maternal plasma for noninvasive detection of sickle cell anemia

artículo científico publicado en 2012

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

artículo científico publicado en 2016

Functional analysis of the breast cancer associated transcriptional repressor PLU-1/JARID1B.

artículo científico publicado en 2006

Gene expression changes induced by a recombinant E1-/E3- adenovirus type 5 vector in human mammary epithelial cells.

artículo científico publicado en 2005

Great vessel development requires biallelic expression of Chd7 and Tbx1 in pharyngeal ectoderm in mice

scientific journal article

Has noninvasive prenatal testing impacted termination of pregnancy and live birth rates of infants with Down syndrome?

artículo científico publicado en 2017

Implementing prenatal diagnosis based on cell-free fetal DNA: accurate identification of factors affecting fetal DNA yield

artículo científico publicado en 2011

Measurement of fetal fraction in cell-free DNA from maternal plasma using a panel of insertion/deletion polymorphisms

artículo científico publicado en 2017

New aids for the non-invasive prenatal diagnosis of achondroplasia: dysmorphic features, charts of fetal size and molecular confirmation using cell-free fetal DNA in maternal plasma.

artículo científico publicado en 2011

Non-invasive foetal RhD genotyping to guide anti-D prophylaxis: an external quality assurance workshop

artículo científico publicado en 2017

Non-invasive prenatal diagnosis of achondroplasia and thanatophoric dysplasia: next-generation sequencing allows for a safer, more accurate, and comprehensive approach.

artículo científico publicado en 2015

Non-invasive prenatal diagnostic testing for β-thalassaemia using cell-free fetal DNA and next generation sequencing.

artículo científico publicado en 2014

Non-invasive prenatal testing for fetal inheritance of maternal β-thalassaemia mutations using targeted sequencing and relative mutation dosage: a feasibility study

artículo científico publicado en 2017

PLU-1 nuclear protein, which is upregulated in breast cancer, shows restricted expression in normal human adult tissues: a new cancer/testis antigen?

artículo científico publicado en 2002

Preferences for prenatal tests for Down syndrome: an international comparison of the views of pregnant women and health professionals

artículo científico publicado en 2015

Safe, accurate, prenatal diagnosis of thanatophoric dysplasia using ultrasound and free fetal DNA.

artículo científico publicado en 2013

Stability of cell-free DNA from maternal plasma isolated following a single centrifugation step

artículo científico

Synthetic combinations of missense polymorphic genetic changes underlying Down syndrome susceptibility.

artículo científico publicado en 2016

Thalassaemia screening and confirmation of carriers in parents.

artículo científico publicado en 2016

The assessment of combined first trimester screening in women of advanced maternal age in an Asian cohort

artículo científico publicado en 2015

The clinical implementation of non-invasive prenatal diagnosis for single-gene disorders: challenges and progress made

artículo científico

Uses of cell free fetal DNA in maternal circulation

artículo científico publicado en 2012

Lista de obras de Angela N Barrett

Application of real-time PCR of sex-independent insertion-deletion polymorphisms to determine fetal sex using cell-free fetal DNA from maternal plasma

Authors' Reply: The assessment of combined first trimester screening in women of advanced maternal age in an Asian cohort.

Biology of human primitive erythroblasts for application in noninvasive prenatal diagnosis

Blood Chimerism in Dizygotic Monochorionic Twins During 5 Years Observation

Breast cancer associated transcriptional repressor PLU-1/JARID1B interacts directly with histone deacetylases

Challenges in non-invasive prenatal screening for sub-chromosomal copy number variations using cell-free DNA.

Detection of aneuploidy from single fetal nucleated red blood cells using whole genome sequencing

Developing noninvasive diagnosis for single-gene disorders: the role of digital PCR.

Digital PCR analysis of maternal plasma for noninvasive detection of sickle cell anemia

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

Functional analysis of the breast cancer associated transcriptional repressor PLU-1/JARID1B.

Gene expression changes induced by a recombinant E1-/E3- adenovirus type 5 vector in human mammary epithelial cells.

Great vessel development requires biallelic expression of Chd7 and Tbx1 in pharyngeal ectoderm in mice

Has noninvasive prenatal testing impacted termination of pregnancy and live birth rates of infants with Down syndrome?

Implementing prenatal diagnosis based on cell-free fetal DNA: accurate identification of factors affecting fetal DNA yield

Measurement of fetal fraction in cell-free DNA from maternal plasma using a panel of insertion/deletion polymorphisms

New aids for the non-invasive prenatal diagnosis of achondroplasia: dysmorphic features, charts of fetal size and molecular confirmation using cell-free fetal DNA in maternal plasma.

Non-invasive foetal RhD genotyping to guide anti-D prophylaxis: an external quality assurance workshop

Non-invasive prenatal diagnosis of achondroplasia and thanatophoric dysplasia: next-generation sequencing allows for a safer, more accurate, and comprehensive approach.

Non-invasive prenatal diagnostic testing for β-thalassaemia using cell-free fetal DNA and next generation sequencing.

Non-invasive prenatal testing for fetal inheritance of maternal β-thalassaemia mutations using targeted sequencing and relative mutation dosage: a feasibility study

PLU-1 nuclear protein, which is upregulated in breast cancer, shows restricted expression in normal human adult tissues: a new cancer/testis antigen?

Preferences for prenatal tests for Down syndrome: an international comparison of the views of pregnant women and health professionals

Safe, accurate, prenatal diagnosis of thanatophoric dysplasia using ultrasound and free fetal DNA.

Stability of cell-free DNA from maternal plasma isolated following a single centrifugation step

Synthetic combinations of missense polymorphic genetic changes underlying Down syndrome susceptibility.

Thalassaemia screening and confirmation of carriers in parents.

The assessment of combined first trimester screening in women of advanced maternal age in an Asian cohort

The clinical implementation of non-invasive prenatal diagnosis for single-gene disorders: challenges and progress made

Uses of cell free fetal DNA in maternal circulation