Anna Capalbo
Foggia, Italy
Last Updated: 09/26/2026
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Found 14 publications
Correction to: Systemic ALK-negative anaplastic large cell lymphoma with distinctive myxoid change and DUSP22 rearrangement.
Journal: Virchows Archiv : an international journal of pathology
Published: August 12, 2022
Positive predictive values and outcomes for uninformative cell-free DNA tests: An Italian multicentric Cytogenetic and cytogenomic Audit of diagnOstic testing (ICARO study).
Journal: Prenatal diagnosis
Published: August 05, 2022
Systemic ALK-negative anaplastic large cell lymphoma with distinctive myxoid change and DUSP22 rearrangement.
Journal: Virchows Archiv : an international journal of pathology
Published: May 25, 2022
Koolen-de Vries syndrome in a 63-year-old woman: Report of the oldest patient and a review of the adult phenotype.
Journal: American journal of medical genetics. Part A
Published: July 30, 2021
Altered Expression of Candidate Genes in Mayer-Rokitansky-Küster-Hauser Syndrome May Influence Vaginal Keratinocytes Biology: A Focus on Protein Kinase X.
Journal: Biology
Published: May 04, 2021
Identification of a De Novo Xq26.2 Microduplication Encompassing FIRRE Gene in a Child with Intellectual Disability.
Journal: Diagnostics (Basel, Switzerland)
Published: October 28, 2020
Protein-protein interaction network analysis applied to DNA copy number profiling suggests new perspectives on the aetiology of Mayer-Rokitansky-Küster-Hauser syndrome.
Journal: Scientific reports
Published: May 11, 2020
De Novo Inverted Duplication Deletion of 4p in a 14-Week-Old Male Fetus Aborted Due to Multiple Anomalies.
Journal: Journal of pediatric genetics
Published: February 14, 2020
Small 7p22.3 microdeletion: Case report of Snx8 haploinsufficiency and neurological findings.
Journal: European journal of medical genetics
Published: March 05, 2019
ALK-negative anaplastic large cell lymphoma with "Hodgkin-like" cytomorphology and nuclear expression of PAX5.
Journal: Pathology, research and practice
Published: October 04, 2018
A novel mosaic 1q32.1 microduplication identified through Chromosome Microarray Analysis: narrowing the smallest critical region including KDM5B gene found associated with neurodevelopmetal disorders.
Journal: European journal of medical genetics
Published: June 10, 2018
An additional clinical sign of 17q21.31 microdeletion syndrome: preaxial polydactyly of hands with broad thumbs.
Journal: American journal of medical genetics. Part A
Published: August 29, 2014
Last Updated: 09/26/2026