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Clinical aspects of Hyaline Fibromatosis Syndrome and identification of a novel mutation.
Mol Genet Genomic Med. 2020 Jun;8(6):e1203. doi: 10.1002/mgg3.1203. Epub 2020 Mar 20.
Mol Genet Genomic Med. 2020.
PMID: 32196989
Free PMC article.
3-M syndrome associated with growth hormone deficiency: 18 year follow-up of a patient.
Meazza C, Lausch E, Pagani S, Bozzola E, Calcaterra V, Superti-Furga A, Silengo M, Bozzola M.
Meazza C, et al. Among authors: lausch e.
Ital J Pediatr. 2013 Mar 21;39:21. doi: 10.1186/1824-7288-39-21.
Ital J Pediatr. 2013.
PMID: 23517720
Free PMC article.
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