Literature DB >> 25332753

Introducing the next generation sequencing in genomic amnio and villuos sampling. The so called "Next Generation Prenatal Diagnosis" (NGPD).

Claudio Giorlandino1, Alvaro Mesoraca2, Domenico Bizzoco2, Claudio Dello Russo2, Antonella Cima2, Gianluca Di Giacomo2, Pietro Cignini1, Francesco Padula1, Nella Dugo1, Laura D'Emidio1, Cristiana Brizzi1, Raffaella Raffio1, Vincenzo Milite1, Lucia Mangiafico1, Claudio Coco1, Ornella Carcioppolo1, Roberto Vigna1, Marialuisa Mastrandrea1, Luisa Mobili1.   

Abstract

Year:  2014        PMID： 25332753      PMCID： PMC4187001     

Source DB:  PubMed          Journal:  J Prenat Med        ISSN： 1971-3282


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  32 in total

1.  Position Statement from the Italian College of Fetal Maternal Medicine: Non-invasive prenatal testing (NIPT) by maternal plasma DNA sequencing.

Authors: 
Journal:  J Prenat Med       Date:  2013-04

2.  The tribunal of modern life: the case of UZ Brussels in the light of Odo Marquard's discussion on autonomy and theodicy.

Authors:  Ignaas Devisch
Journal:  J Eval Clin Pract       Date:  2013-06       Impact factor: 2.431

Review 3.  Cell-free fetal DNA and RNA in maternal blood: implications for safer antenatal testing.

Authors:  Caroline F Wright; Lyn S Chitty
Journal:  BMJ       Date:  2009-07-06

Review 4.  Clinical practice. Prenatal screening for aneuploidy.

Authors:  Deborah A Driscoll; Susan Gross
Journal:  N Engl J Med       Date:  2009-06-11       Impact factor: 91.245

Review 5.  Use of a DNA method, QF-PCR, in the prenatal diagnosis of fetal aneuploidies.

Authors:  Sylvie Langlois; Alessandra Duncan
Journal:  J Obstet Gynaecol Can       Date:  2011-09

6.  Echogenic intracardiac foci: disclosure and the rate of amniocentesis in low-risk patients.

Authors:  Stephen T Chasen; Armin S Razavi
Journal:  Am J Obstet Gynecol       Date:  2013-10       Impact factor: 8.661

Review 7.  Early detection of hearing impairment in newborns and infants.

Authors:  Martin Ptok
Journal:  Dtsch Arztebl Int       Date:  2011-06-24       Impact factor: 5.594

8.  The physician's breach of the duty to inform the parent of deformities and abnormalities in the foetus: "wrongful life" actions, a new frontier of medical responsibility.

Authors:  Paola Frati; Matteo Gulino; Emanuela Turillazzi; Simona Zaami; Vittorio Fineschi
Journal:  J Matern Fetal Neonatal Med       Date:  2013-10-31

9.  First-trimester diagnosis of Meckel-Gruber syndrome by fetal ultrasound with molecular identification of CC2D2A mutations by next-generation sequencing.

Authors:  D Jones; F Fiozzo; B Waters; D McKnight; S Brown
Journal:  Ultrasound Obstet Gynecol       Date:  2014-10-27       Impact factor: 7.299

10.  Exome sequencing improves genetic diagnosis of structural fetal abnormalities revealed by ultrasound.

Authors:  Keren J Carss; Sarah C Hillman; Vijaya Parthiban; Dominic J McMullan; Eamonn R Maher; Mark D Kilby; Matthew E Hurles
Journal:  Hum Mol Genet       Date:  2014-01-29       Impact factor: 6.150
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  1 in total

1.  Next Generation Sequencing Approach in a Prenatal Case of Cardio-Facio-Cutaneus Syndrome.

Authors:  Mafalda Mucciolo; Claudio Dello Russo; Laura D'Emidio; Alvaro Mesoraca; Claudio Giorlandino
Journal:  Int J Mol Sci       Date:  2016-06-16       Impact factor: 5.923
  1 in total

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