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International Journal of Molecular Sciences
|
June 21, 2016
Next Generation Sequencing Approach in a Prenatal Case of Cardio-Facio-Cutaneus Syndrome
Mafalda Mucciolo, Claudio Dello Russo, Laura D'Emidio, et al.
Journal of Prenatal Medicine
|
October 22, 2014
Next generation sequencing in the identification of a rare genetic disease from preconceptional couple screening to preimplantation genetic diagnosis
Claudio Dello Russo, Gianluca Di Giacomo, Alvaro Mesoraca, et al.
BMC Research Notes
|
March 20, 2020
Cell-free DNA screening for sex chromosomal aneuploidies in 9985 pregnancies: Italian single experience
Katia Margiotti, Anthony Cesta, Claudio Dello Russo, et al.
The Journal of Molecular Diagnostics : JMD
|
April 28, 2019
Validation of Extensive Next-Generation Sequencing Method for Monogenic Disorder Analysis on Cell-Free Fetal DNA: Noninvasive Prenatal Diagnosis
Claudio Dello Russo, Anthony Cesta, Salvatore Longo, et al.
Journal of Medicine and Life
|
January 18, 2021
Cytogenetics and Molecular Investigations detect a Mosaic Variant of Turner Syndrome only Suspected by Non-Invasive Prenatal Testing: Two Case Reports with Negative Ultrasound Examinations
Francesco Libotte, Sonia Lorena Carpineto, Claudio Dello Russo, et al.
Molecular Biology of the Cell
|
November 30, 2007
PP2A regulates HDAC4 nuclear import
Gabriela Paroni, Nadia Cernotta, Claudio Dello Russo, et al.
Genetics Research
|
June 17, 2020
Cell-free DNA screening for aneuploidies in 7113 pregnancies: single Italian centre study
Alvaro Mesoraca, Katia Margiotti, Claudio Dello Russo, et al.
Diagnostics (Basel, Switzerland)
|
September 27, 2025
<i>NUAK2</i> Pathogenic Variants Are Definitively Associated with Neural Tube Defects in Humans: New Genotype-Phenotype Correlation and Review of the Literature
Gioia Mastromoro, Claudio Dello Russo, Stefania Mariani, et al.
Journal of Prenatal Medicine
|
August 13, 2015
Comparative study of aCGH and Next Generation Sequencing (NGS) for chromosomal microdeletion and microduplication screening
Claudio Dello Russo, Gianluca Di Giacomo, Pietro Cignini, et al.
Cancer Research
|
July 23, 2009
Loss of histone deacetylase 4 causes segregation defects during mitosis of p53-deficient human tumor cells
Bruno Cadot, Mirko Brunetti, Sabina Coppari, et al.
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of 2
Search research articles
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Showing results (1-10 of 12) with videos related to
Sort By:
Page
of 2
International Journal of Molecular Sciences
|
June 21, 2016
Next Generation Sequencing Approach in a Prenatal Case of Cardio-Facio-Cutaneus Syndrome
Mafalda Mucciolo, Claudio Dello Russo, Laura D'Emidio, et al.
Journal of Prenatal Medicine
|
October 22, 2014
Next generation sequencing in the identification of a rare genetic disease from preconceptional couple screening to preimplantation genetic diagnosis
Claudio Dello Russo, Gianluca Di Giacomo, Alvaro Mesoraca, et al.
BMC Research Notes
|
March 20, 2020
Cell-free DNA screening for sex chromosomal aneuploidies in 9985 pregnancies: Italian single experience
Katia Margiotti, Anthony Cesta, Claudio Dello Russo, et al.
The Journal of Molecular Diagnostics : JMD
|
April 28, 2019
Validation of Extensive Next-Generation Sequencing Method for Monogenic Disorder Analysis on Cell-Free Fetal DNA: Noninvasive Prenatal Diagnosis
Claudio Dello Russo, Anthony Cesta, Salvatore Longo, et al.
Journal of Medicine and Life
|
January 18, 2021
Cytogenetics and Molecular Investigations detect a Mosaic Variant of Turner Syndrome only Suspected by Non-Invasive Prenatal Testing: Two Case Reports with Negative Ultrasound Examinations
Francesco Libotte, Sonia Lorena Carpineto, Claudio Dello Russo, et al.
Molecular Biology of the Cell
|
November 30, 2007
PP2A regulates HDAC4 nuclear import
Gabriela Paroni, Nadia Cernotta, Claudio Dello Russo, et al.
Genetics Research
|
June 17, 2020
Cell-free DNA screening for aneuploidies in 7113 pregnancies: single Italian centre study
Alvaro Mesoraca, Katia Margiotti, Claudio Dello Russo, et al.
Diagnostics (Basel, Switzerland)
|
September 27, 2025
<i>NUAK2</i> Pathogenic Variants Are Definitively Associated with Neural Tube Defects in Humans: New Genotype-Phenotype Correlation and Review of the Literature
Gioia Mastromoro, Claudio Dello Russo, Stefania Mariani, et al.
Journal of Prenatal Medicine
|
August 13, 2015
Comparative study of aCGH and Next Generation Sequencing (NGS) for chromosomal microdeletion and microduplication screening
Claudio Dello Russo, Gianluca Di Giacomo, Pietro Cignini, et al.
Cancer Research
|
July 23, 2009
Loss of histone deacetylase 4 causes segregation defects during mitosis of p53-deficient human tumor cells
Bruno Cadot, Mirko Brunetti, Sabina Coppari, et al.
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of 2