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1.685 Aktuelle Fachpublikationen aus der Branche Diagnostik

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Utility of chromosomal microarray in anomalous fetuses

03.01.2018 | Jacqueline G. Parchem, Teresa N. Sparks, Kristen Gosnell, Mary E. Norton, Prenatal Diagnosis, 2018

Abstract Objective To determine the association of copy number variants (CNV) with perinatal outcomes among fetuses with sonographic abnormalities. Methods This was a retrospective cohort study of anomalous fetuses evaluated at a single fetal center, who underwent chromosomal ...

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29.12.2017 | Prenatal Diagnosis, 2017

No abstract is available for this article.

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22.12.2017 | Prenatal Diagnosis, 2017

No abstract is available for this article.

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Delivering an accredited non‐invasive prenatal diagnosis service for monogenic disorders, and recommendations for best practice

20.12.2017 | Lucy A. Jenkins, Zandra C. Deans, Celine Lewis, Stephanie Allen, Prenatal Diagnosis, 2017

Abstract The identification of cell free fetal DNA circulating in maternal blood combined with technological developments, in particular next generation sequencing, is enabling the development of safer prenatal diagnosis. Whilst this technology has been widely applied as a highly sensitive ...

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19.09.2017 | Prenatal Diagnosis, 2017

No abstract is available for this article.

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A systematic review and meta‐analysis on fetal ovarian cysts: impact of size, appearance and prenatal aspiration.

08.09.2017 | Athanasios Tyraskis, Spyros Bakalis, Anna L. David, Simon Eaton, Paolo De Coppi, Prenatal Diagnosis, 2017

Abstract Objective To compare outcomes of ultrasound‐guided aspiration of fetal ovarian cysts with conservative management. Method A systematic review of MEDLINE and Web of Science included studies reporting outcomes (pre‐ and post‐natal torsion, spontaneous resolution, and surgery) ...

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On the road to replacing invasive testing with cell‐based NIPT: five clinical cases with aneuploidies, microduplication, unbalanced structural rearrangement or mosaicism

07.09.2017 | Else Marie Vestergaard, Ripudaman Singh, Palle Schelde, Lotte Hatt, Katarina Ravn, Rikke Christensen, Dorte Launholt ..., Prenatal Diagnosis, 2017

Abstract Objective Trophoblastic fetal cells harvested from maternal blood have the capacity to be used for copy number analyses in a non‐invasive prenatal test (cbNIPT). Potentially this will result in increased resolution for detection of subchromosomal aberrations due to high quality DNA ...

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The association between anticoagulation therapy, maternal characteristics, and a failed cfDNA test due to a low fetal fraction

07.09.2017 | Whitney Burns, Nathanael Koelper, Andrea Barberio, Mary DeAgostino‐Kelly, Michael Mennuti, Mary D. Sammel, Lorraine ..., Prenatal Diagnosis, 2017

Abstract Objectives The objective of this study was to identify maternal characteristics associated with a failed cell‐free DNA (cfDNA) test due to a low fetal fraction (FF). Method Retrospective cohort study of women with singleton pregnancies who had cfDNA screening at 10‐25 weeks ...

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Group genetic counseling: an alternate service delivery model in a high risk prenatal screening population

05.09.2017 | Mireille Cloutier, Lauren Gallagher, Claire Goldsmith, Salwa Akiki, Nick Barrowman, Shawna Morrison, Prenatal Diagnosis, 2017

Abstract Objective To address the growing demand for prenatal genetics services, group genetic counseling was explored as an alternative service delivery model for women with a positive prenatal screening result. Method Women were recruited from a prenatal genetics service and ...

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The amniotic fluid as a source of mesenchymal stem cells with lung‐specific characteristics

26.08.2017 | Flore Lesage, Silvia Zia, Julio Jiménez, Jan Deprest, Jaan Toelen, Prenatal Diagnosis, 2017

Abstract The amniotic fluid is a clinically accessible source of mesenchymal stem cells (AF‐MSC) during gestation, which enables autologous cellular therapy for perinatal disorders. The origin of AF‐MSC remains elusive: renal and neuronal progenitors have been isolated from the AF‐MSC pool, ...

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