Maria Francesca Bedeschi

6PUBLICATIONS
12CO-AUTHORS
Food properties (incl. characteristics and health benefits)Cardiology (incl. cardiovascular diseases)OrthopaedicsEpigenetics (incl. genome methylation and epigenomics)Developmental genetics (incl. sex determination)
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Publications (6)

|Jan 27, 2025
Phenotypical Characterization of Gastroenterological and Metabolic Manifestations in Patients With Williams-Beuren Syndrome.

Maria Francesca Bedeschi, Annarita Baldassarri, Roberta Villa

|Jul 15, 2024
Reviewing hereditary connective tissue disorders: Proposals of harmonic medicolegal assessments.

Nicola Galante, Maria Francesca Bedeschi, Benedetta Beltrami

|Nov 23, 2022
Congenital diaphragmatic hernia in Coffin Siris syndrome: Further evidence from two cases.

Martina Rimoldi, Berardo Rinaldi, Roberta Villa

|Oct 18, 2022
Celiac disease prevalence and predisposing-HLA in a cohort of 93 Williams-Beuren syndrome patients.

Cecilia Ghisleni, Barbara Parma, Paola Cianci

|Jul 31, 2019
Phenotype delineation of ZNF462 related syndrome.

Paul Kruszka, Tommy Hu, Sungkook Hong

|Nov 01, 2017
STAR syndrome plus: The first description of a female patient with the lethal form.

Maria F Bedeschi, Sara Giangiobbe, Leda Paganini

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Frequent Collaborators

2 joint publications

Benedetta Beltrami

1 joint publications

Paul Kruszka

1 joint publications

Julian A Martinez-Agosto

1 joint publications

Kym Boycott