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im Bestand: Gesamter Bestand

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Artikel 1 Cherubism as a systemic skeletal disease: evidence from an aggressive case
Enthalten in BMC musculoskeletal disorders Bd. 21, 21.8.2020, Nr. 1, date:12.2020: 1-8
Online Ressource
Artikel 2 Cluster analysis unveils a severe persistent respiratory impairment phenotype 3-months after severe COVID-19
Enthalten in Respiratory research Bd. 23, 2.8.2022, Nr. 1, date:12.2022: 1-10
Online Ressource
Artikel 3 Gynecological issues in children and adolescents seen at rare-disease referral centers: an observational retrospective cohort study
Enthalten in Orphanet journal of rare diseases Bd. 20, 11.3.2025, Nr. 1, date:12.2025: 1-9
Online Ressource
Artikel 4 Next generation phenotyping for diagnosis and phenotype–genotype correlations in Kabuki syndrome
Enthalten in Scientific reports Bd. 14, 28.1.2024, Nr. 1, date:12.2024: 1-15
Online Ressource
Artikel 5 Next generation phenotyping using narrative reports in a rare disease clinical data warehouse
Enthalten in Orphanet journal of rare diseases Bd. 13, 31.5.2018, Nr. 1, date:12.2018: 1-11
Online Ressource
Artikel 6 Quality of life and phonatory and morphological outcomes in cognitively unimpaired adolescents with Pierre Robin sequence: a cross-sectional study of 72 patients
Enthalten in Orphanet journal of rare diseases Bd. 16, 20.10.2021, Nr. 1, date:12.2021: 1-15
Online Ressource


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