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RESEARCH PRODUCT
De-novo Williams–Beuren and inherited Marfan syndromes in a patient with developmental delay and lens dislocation
Magdalena BudisteanuAndreea Tutulan-cunitaSorina Mihaela PapucAurora ArghirUlrich ZechnerEva WeisOliver BartschBogdan Budisteanusubject
MaleWilliams Syndrome0301 basic medicinePediatricsmedicine.medical_specialtyGenotypeDevelopmental DisabilitiesFibrillin-1DNA Mutational AnalysisMarfan SyndromePathology and Forensic Medicine03 medical and health sciencesDislocation (syntax)medicineHumansChildAllelesIn Situ Hybridization FluorescenceGenetics (clinical)Myosin Heavy Chainsbusiness.industryFaciesGeneral MedicineLens SubluxationPhenotype030104 developmental biologymedicine.anatomical_structureLens (anatomy)MutationPediatrics Perinatology and Child HealthAnatomybusinessyear | journal | country | edition | language |
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2017-03-10 | Clinical Dysmorphology |