Works by Alfonsi, Melissa

Results: 14

Deletion 18p11.32p11.31 in a Child with Global Developmental Delay and Atypical, Drug-Resistant Absence Seizures.

Published in:

Cytogenetic & Genome Research, 2015, v. 146, n. 2, p. 115, doi. 10.1159/000438502

By:

Verrotti, alberto;
Palka, Chiara;
Prezioso, Giovanni;
alfonsi, Melissa;
Calabrese, Giuseppe;
Palka, Giandomenico;
Chiarelli, Francesco

Publication type:

Article

Mayer-Rokitansky-Küster-Hauser syndrome with 22q11.21 microduplication: a case report.

Published in:

2021

By:

Dell'Edera, Domenico;
Allegretti, Arianna;
Ventura, Mario;
Mercuri, Ludovica;
Mitidieri, Angela;
Cuscianna, Giacinto;
Epifania, Annunziata Anna;
Morizio, Elisena;
Alfonsi, Melissa;
Guanciali-Franchi, Paolo

Publication type:

journal article

Indirect Co-Culture with Tendons or Tenocytes Can Program Amniotic Epithelial Cells towards Stepwise Tenogenic Differentiation.

Published in:

PLoS ONE, 2012, v. 7, n. 2, p. 1, doi. 10.1371/journal.pone.0030974

By:

Barboni, Barbara;
Curini, Valentina;
Russo, Valentina;
Mauro, Annunziata;
Di Giacinto, Oriana;
Marchisio, Marco;
Alfonsi, Melissa;
Mattioli, Mauro

Publication type:

Article

Case report of newborn with <bold><italic>de novo</italic></bold> partial trisomy 2q31.2-37.3 and monosomy 9p24.3.

Published in:

Journal of Genetics, 2018, v. 97, n. 1, p. 311, doi. 10.1007/s12041-017-0879-3

By:

Colangelo, Maurizia;
Alfonsi, Melissa;
Palka, Chiara;
Zio, Eleonora Di;
Renzo, Silvana Di;
Guanciali-Franchi, Paolo;
Palka, Giandomenico

Publication type:

Article

Sequential combined test, second trimester maternal serum markers, and circulating fetal cells to select women for invasive prenatal diagnosis.

Published in:

PLoS ONE, 2017, v. 12, n. 12, p. 1, doi. 10.1371/journal.pone.0189235

By:

Guanciali Franchi, Paolo;
Palka, Chiara;
Morizio, Elisena;
Sabbatinelli, Giulia;
Alfonsi, Melissa;
Fantasia, Donatella;
Sitar, Giammaria;
Benn, Peter;
Calabrese, Giuseppe

Publication type:

Article

Testing single/combined clinical categories on 5110 Italian patients with developmental phenotypes to improve array‐based detection rate.

Published in:

Molecular Genetics & Genomic Medicine, 2020, v. 8, n. 1, p. N.PAG, doi. 10.1002/mgg3.1056

By:

Catusi, Ilaria;
Recalcati, Maria Paola;
Bestetti, Ilaria;
Garzo, Maria;
Valtorta, Chiara;
Alfonsi, Melissa;
Alghisi, Alberta;
Cappellani, Stefania;
Casalone, Rosario;
Caselli, Rossella;
Ceccarini, Caterina;
Ceglia, Carlo;
Ciaschini, Anna Maria;
Coviello, Domenico;
Crosti, Francesca;
D'Aprile, Annamaria;
Fabretto, Antonella;
Genesio, Rita;
Giagnacovo, Marzia;
Granata, Paola

Publication type:

Article

Aneuploidy screening using circulating fetal cells in maternal blood by dual-probe FISH protocol: a prospective feasibility study on a series of 172 pregnant women.

Published in:

Molecular Genetics & Genomic Medicine, 2016, v. 4, n. 6, p. 634, doi. 10.1002/mgg3.249

By:

Calabrese, Giuseppe;
Fantasia, Donatella;
Alfonsi, Melissa;
Morizio, Elisena;
Celentano, Claudio;
Guanciali Franchi, Paolo;
Sabbatinelli, Giulia;
Palka, Chiara;
Benn, Peter;
Sitar, Gianmaria

Publication type:

Article

Yq Microdeletion in a Patient with VACTERL Association and Shawl Scrotum with Bifid Scrotum: A Real Pathogenetic Association or a Coincidence?

Published in:

Cytogenetic & Genome Research, 2019, v. 158, n. 3, p. 121, doi. 10.1159/000501601

By:

Tumini, Stefano;
alfonsi, Melissa;
Carinci, Silvia;
Morizio, Elisena;
antonucci, Ivana;
Gatta, Valentina;
Lisi, Gabriele;
Lelli Chiesa, Pierluigi;
Calabrese, Giuseppe;
Stuppia, Liborio;
Palka, Chiara

Publication type:

Article

Optimal cut-offs for Down syndrome contingent screening in a population of 10,156 pregnant women.

Published in:

2012

By:

Guanciali-Franchi P;
Iezzi I;
Soranno A;
de Volo CP;
Alfonsi M;
Calabrese G;
Benn P;
Guanciali-Franchi, Paolo;
Iezzi, Irene;
Soranno, Alessandra;
de Volo, Chiara Palka-Bayard;
Alfonsi, Melissa;
Calabrese, Giuseppe;
Benn, Peter

Publication type:

journal article

Optimal cut-offs for down syndrome contingent screening in a population of 10 156 pregnant women.

Published in:

Prenatal Diagnosis, 2012, v. 32, n. 12, p. 1147, doi. 10.1002/pd.3974

By:

Guanciali-Franchi, Paolo;
Iezzi, Irene;
Soranno, Alessandra;
Volo, Chiara Palka-Bayard;
Alfonsi, Melissa;
Calabrese, Giuseppe;
Benn, Peter

Publication type:

Article

First case of two supernumerary markers derived from chromosome 5 and chromosome 8.

Published in:

Molecular Cytogenetics (17558166), 2022, v. 15, n. 1, p. 1, doi. 10.1186/s13039-022-00601-5

By:

Giansante, Roberta;
Palka Bayard De Volo, Chiara;
Alfonsi, Melissa;
Morizio, Elisena;
Guanciali Franchi, Paolo

Publication type:

Article

Isolation and Enrichment of Circulating Fetal Cells for NIPD: An Overview.

Published in:

Diagnostics (2075-4418), 2021, v. 11, n. 12, p. 2239, doi. 10.3390/diagnostics11122239

By:

Sabbatinelli, Giulia;
Fantasia, Donatella;
Palka, Chiara;
Morizio, Elisena;
Alfonsi, Melissa;
Calabrese, Giuseppe

Publication type:

Article

An 11.4-Mb Interstitial Deletion in a Fetus with No Apparent Phenotypic Alterations.

Published in:

Molecular Syndromology, 2017, v. 8, n. 1, p. 42, doi. 10.1159/000452967

By:

Guanciali-Franchi, Paolo;
Celentano, Claudio;
Alfonsi, Melissa;
Palka, Chiara;
Di Pasqua, Giulietta;
Matarrelli, Barbara;
Palka, Giandomenico

Publication type:

Article

1q21.1 Duplication Syndrome and Anorectal Malformations: A Literature Review and a New Case.

Published in:

2025

By:

Minelli, Maria;
Palka Bayard de Volo, Chiara;
Alfonsi, Melissa;
Capanna, Serena;
Morizio, Elisena;
Miscia, Maria Enrica;
Lisi, Gabriele;
Stuppia, Liborio;
Gatta, Valentina

Publication type:

Case Study