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1. Complex chromosomal rearrangements causing Langer–Giedion syndrome atypical phenotype: Genotype–phenotype correlation and literature review. Issue 3 (19th December 2013)

2. First trimester ultrasound features of X-linked Opitz syndrome and early molecular diagnosis: case report and review of the literature. (17th September 2021)

3. Hmga1 null mouse embryonic fibroblasts display downregulation of spindle assembly checkpoint gene expression associated to nuclear and karyotypic abnormalities. Issue 6 (18th March 2016)

4. Metformin restores the mitochondrial network and reverses mitochondrial dysfunction in Down syndrome cells. (13th January 2017)

5. Overexpression of Chromosome 21 miRNAs May Affect Mitochondrial Function in the Hearts of Down Syndrome Fetuses. (5th September 2017)

6. Prenatally diagnosed distal 16p11.2 microdeletion with a novel association with congenital diaphragmatic hernia: a case report. Issue 4 (9th February 2018)

7. Rab7 Regulates CDH1 Endocytosis, Circular Dorsal Ruffles Genesis, and Thyroglobulin Internalization in a Thyroid Cell Line. Issue 8 (10th December 2015)