Publications by authors named "Valentina Ronga"

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Polymorphic Rearrangements of Human Chromosome 9 and Male Infertility: New Evidence and Impact on Spermatogenesis.
Filomena Mottola, Marianna Santonastaso, Valentina Ronga, Renata Finelli, Lucia Rocco

Biomolecules· April 2023

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DNA Damage in Human Amniotic Cells: Antigenotoxic Potential of Curcumin and -Lipoic Acid.
Filomena Mottola, Marianna Santonastaso, Concetta Iovine, Cristina Rossetti, Valentina Ronga

Antioxidants (Basel)· July 2021

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Complex chromosomal rearrangements causing Langer-Giedion syndrome atypical phenotype: genotype-phenotype correlation and literature review.
Gerarda Cappuccio, Rita Genesio, Valentina Ronga, Alberto Casertano, Antonella Izzo

Am J Med Genet A· March 2014

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Pure 16q21q22.1 deletion in a complex rearrangement possibly caused by a chromothripsis event.
Rita Genesio, Valentina Ronga, Pia Castelluccio, Gennaro Fioretti, Angela Mormile

Mol Cytogenet· August 2013

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Immunoglobulin heavy-chain fluorescence in situ hybridization-chromogenic in situ hybridization DNA probe split signal in the clonality assessment of lymphoproliferative processes on cytological samples.
Pio Zeppa, Laura Virginia Sosa Fernandez, Immacolata Cozzolino, Valentina Ronga, Rita Genesio

Cancer Cytopathol· December 2012

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Clinical description of a patient carrying the smallest reported deletion involving 10p14 region.
Daniela Melis, Rita Genesio, Pasquale Boemio, Ennio Del Giudice, Gerarda Cappuccio, Valentina Ronga

Am J Med Genet A· April 2012

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Variegated silencing through epigenetic modifications of a large Xq region in a case of balanced X;2 translocation with Incontinentia Pigmenti-like phenotype.
Rita Genesio, Daniela Melis, Sole Gatto, Antonella Izzo, Valentina Ronga

Epigenetics· October 2011

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An emerging phenotype of proximal 11q deletions.
Daniela Melis, Rita Genesio, Mariarosaria Cozzolino, Ennio Del Giudice, Angela Mormile, Valentina Ronga

Eur J Med Genet· January 2011

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