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A large deletion (1.5 Mb) encompassing the neurofibromatosis type 1 (NF1) gene in a patient with sporadic NF1 associated with dysmorphism, mental retardation, and unusual ocular and skeletal features.

dc.contributor.authorULUCAN, Hakan
dc.date.accessioned2021-03-05T12:33:52Z
dc.date.available2021-03-05T12:33:52Z
dc.identifier.citationULUCAN H., "A large deletion (1.5 Mb) encompassing the neurofibromatosis type 1 (NF1) gene in a patient with sporadic NF1 associated with dysmorphism, mental retardation, and unusual ocular and skeletal features.", CLINICAL DYSMORPHOLOGY, cilt.12, ss.199-201, 2003
dc.identifier.issn0962-8827
dc.identifier.otherav_adccadb8-f183-4493-840e-07fd26473565
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/115954
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/pubmed/14564162
dc.language.isoeng
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectKlinik Tıp (MED)
dc.titleA large deletion (1.5 Mb) encompassing the neurofibromatosis type 1 (NF1) gene in a patient with sporadic NF1 associated with dysmorphism, mental retardation, and unusual ocular and skeletal features.
dc.typeMakale
dc.relation.journalCLINICAL DYSMORPHOLOGY
dc.contributor.departmentİstanbul Üniversitesi , ,
dc.identifier.volume12
dc.identifier.startpage199
dc.identifier.endpage201
dc.contributor.firstauthorID618714


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