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1. Expanding the clinical spectrum associated with the PACS1 p.Arg203Trp mutational hot‐spot: Two additional Italian patients

2. Natural history of KBG syndrome in a large European cohort

3. Natural history of KBG syndrome in a large European cohort

5. Shorter androgen receptor polyQ alleles protect against life-threatening COVID-19 disease in European males

6. Corrigendum: Exome Sequencing in BRCA1-2 Candidate Familias: The Contribution of Other Cancer Susceptibility Genes.

7. Sporadic hereditary motor and sensory neuropathies: Advances in the diagnosis using next generation sequencing technology

8. Interstitial 22q13 deletions not involving SHANK3 gene: A new contiguous gene syndrome

11. Chromosomal contacts connect loci associated with autism, BMI and head circumference phenotypes

12. Expanding the clinical spectrum associated with the <scp> PACS1 </scp> p. <scp>Arg203Trp</scp> mutational hot‐spot: Two additional Italian patients

13. A first update on mapping the human genetic architecture of COVID-19

14. Natural history of KBG syndrome in a large European cohort

15. First identification of a triple corneal dystrophy association: keratoconus, epithelial basement membrane corneal dystrophy and fuchs' endothelial corneal dystrophy.

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