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Congenital hypertelorism & osteopenia, a novel autosomal recessive disease of development

dc.contributor.authorShboul, Mohammad
dc.contributor.authorKayserili, Hulya
dc.contributor.authorReversade, Bruno
dc.contributor.authorHamamy, Hanan
dc.contributor.authorLee, Hane
dc.contributor.authorMerriman, Barry
dc.contributor.authorBonnard, Carine
dc.contributor.authorAkarsu, Nurten
dc.date.accessioned2021-03-05T14:25:19Z
dc.date.available2021-03-05T14:25:19Z
dc.identifier.citationBonnard C., Shboul M., Akarsu N., Kayserili H., Merriman B., Lee H., Hamamy H., Reversade B., "Congenital hypertelorism & osteopenia, a novel autosomal recessive disease of development", 16th Annual Conference of the International-Society-of-Development-Biologists, Edinburgh, Saint Helena, 6 - 10 Eylül 2009, cilt.126
dc.identifier.othervv_1032021
dc.identifier.otherav_b711277a-7acb-4131-a02a-27d982b94d7e
dc.identifier.urihttp://hdl.handle.net/20.500.12627/121849
dc.identifier.urihttps://doi.org/10.1016/j.mod.2009.06.255
dc.language.isoeng
dc.subjectTemel Bilimler
dc.subjectYaşam Bilimleri
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectMikrobiyal Genetik
dc.subjectGELİŞİMSEL BİYOLOJİ
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectYaşam Bilimleri (LIFE)
dc.titleCongenital hypertelorism & osteopenia, a novel autosomal recessive disease of development
dc.typeBildiri
dc.contributor.departmentAgency for Science Technology & Research (ASTAR) , ,
dc.identifier.volume126
dc.contributor.firstauthorID136111


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