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2021 | 1 |
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Page 1
Dermatological findings in Rubinstein-Taybi Syndrome.
Ital J Dermatol Venerol. 2023 Aug;158(4):316-320. doi: 10.23736/S2784-8671.23.07547-3. Epub 2023 Jun 7.
Ital J Dermatol Venerol. 2023.
PMID: 37282850
Free article.
Review.
Clinical and Genetic Aspects of Phelan-McDermid Syndrome: An Interdisciplinary Approach to Management.
Cammarata-Scalisi F, Callea M, Martinelli D, Willoughby CE, Tadich AC, Araya Castillo M, Lacruz-Rengel MA, Medina M, Grimaldi P, Bertini E, Nevado J.
Cammarata-Scalisi F, et al. Among authors: araya castillo m.
Genes (Basel). 2022 Mar 12;13(3):504. doi: 10.3390/genes13030504.
Genes (Basel). 2022.
PMID: 35328058
Free PMC article.
Review.
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A Severe Case of Spondylometaphyseal Dysplasia Algerian Type with Two Mutations in COL2A1.
Cammarata-Scalisi F, Matysiak U, Willoughby CE, Ruzaike G, Cárdenas Tadich A, Araya Castillo M, Zara-Chirinos C, Bracho A, Avendaño A, Jilani H, Callea M.
Cammarata-Scalisi F, et al. Among authors: araya castillo m.
J Pediatr Genet. 2021 Jul 26;12(4):339-341. doi: 10.1055/s-0041-1732474. eCollection 2023 Dec.
J Pediatr Genet. 2021.
PMID: 38162154
Free PMC article.
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Novel EDA mutations cause X-linked hypohidrotic ectodermal dysplasia: the first study from Venezuela.
Cammarata-Scalisi F, Callea M, Chaudhary AK, Tadich AC, Castillo MA, Morabito A, Bellacchio E, Pisaneschi E, Novelli A, Willoughby CE, Bashyam MD.
Cammarata-Scalisi F, et al. Among authors: castillo ma.
Clin Exp Dermatol. 2023 Nov 16;48(12):1409-1413. doi: 10.1093/ced/llad218.
Clin Exp Dermatol. 2023.
PMID: 37379583
No abstract available.
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