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dc.contributor.authorCockerham, John
dc.contributor.authorULUCAN, Hakan
dc.contributor.authorSapp, Julie C.
dc.contributor.authorJohnston, Jennifer J.
dc.contributor.authorBiesecker, Leslie G.
dc.contributor.authorGuel, Davut
dc.date.accessioned2021-03-04T19:25:16Z
dc.date.available2021-03-04T19:25:16Z
dc.identifier.citationULUCAN H., Guel D., Sapp J. C. , Cockerham J., Johnston J. J. , Biesecker L. G. , "Extending the spectrum of Ellis van Creveld syndrome: a large family with a mild mutation in the EVC gene", BMC MEDICAL GENETICS, cilt.9, 2008
dc.identifier.issn1471-2350
dc.identifier.othervv_1032021
dc.identifier.otherav_8faf8492-f2bd-4d9e-95ec-780af930f96c
dc.identifier.urihttp://hdl.handle.net/20.500.12627/97018
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/pubmed/18947413
dc.identifier.urihttps://doi.org/10.1186/1471-2350-9-92
dc.description.abstractBackground: Ellis-van Creveld (EvC) syndrome is characterized by short limbs, short ribs, postaxial polydactyly, dysplastic nails and teeth and is inherited in an autosomal recessive pattern. We report a family with complex septal cardiac defects, rhizomelic limb shortening, and polydactyly, without the typical lip, dental, and nail abnormalities of EvC. The phenotype was inherited in an autosomal recessive pattern, with one instance of pseudodominant inheritance.
dc.language.isoeng
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectTemel Bilimler
dc.subjectTıbbi Genetik
dc.subjectYaşam Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectSağlık Bilimleri
dc.subjectTıp
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectGENETİK VE HAYAT
dc.titleExtending the spectrum of Ellis van Creveld syndrome: a large family with a mild mutation in the EVC gene
dc.typeMakale
dc.relation.journalBMC MEDICAL GENETICS
dc.contributor.departmentGulhane Military Medical Academy , ,
dc.identifier.volume9
dc.contributor.firstauthorID727713


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