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Clinical next generation sequencing in developmental and epileptic encephalopathies: Diagnostic relevance of data re-analysis and variants re-interpretation.
Eur J Med Genet. 2021 Dec;64(12):104363. doi: 10.1016/j.ejmg.2021.104363. Epub 2021 Oct 18.
Eur J Med Genet. 2021.
PMID: 34673242
Chromosome rearrangements among couples with pregnancy losses and other adverse reproductive outcomes.
Gadow EC, Lippold S, Otano L, Serafin E, Scarpati R, Matayoshi T.
Gadow EC, et al.
Am J Med Genet. 1991 Dec 1;41(3):279-81. doi: 10.1002/ajmg.1320410303.
Am J Med Genet. 1991.
PMID: 1789279
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Prenatal diagnosis and long survival of Fryns' syndrome.
Gadow EC, Lippold S, Serafin E, Salgado LJ, Garcia C, Prudent L.
Gadow EC, et al.
Prenat Diagn. 1994 Aug;14(8):673-6. doi: 10.1002/pd.1970140806.
Prenat Diagn. 1994.
PMID: 7991509
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Happle-Tinschert syndrome variable phenotype as part of the mosaic hedgehog spectrum: Report of three cases.
Cano R, Abad ME, Schanze D, Zenker M, Serafin E, Larralde M.
Cano R, et al.
Pediatr Dermatol. 2023 Jul-Aug;40(4):691-694. doi: 10.1111/pde.15248. Epub 2023 Jan 27.
Pediatr Dermatol. 2023.
PMID: 36707059
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Use of PET-CT Imaging to Identify Femoral-Popliteal Stent Infection .
Chen AM, Serafin EM, Motaganahalli RL.
Chen AM, et al. Among authors: serafin em.
Vasc Endovascular Surg. 2019 May;53(4):341-342. doi: 10.1177/1538574419831479. Epub 2019 Mar 5.
Vasc Endovascular Surg. 2019.
PMID: 30836853
Free article.
No abstract available.
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