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Response to Kouwenberg et al. "Recognizable Phenotype With Common Occurrence of Microcephaly, Psychomotor Retardation, But No Spontaneous Bone Fractures in ARCL2B Due to PYCR1 Mutations"

dc.contributor.authorTolun, Aslihan
dc.contributor.authorTuysuz, Beyhan
dc.contributor.authorYildirim, Yeserin
dc.date.accessioned2021-03-05T21:30:31Z
dc.date.available2021-03-05T21:30:31Z
dc.date.issued2011
dc.identifier.citationTuysuz B., Tolun A., Yildirim Y., "Response to Kouwenberg et al. "Recognizable Phenotype With Common Occurrence of Microcephaly, Psychomotor Retardation, But No Spontaneous Bone Fractures in ARCL2B Due to PYCR1 Mutations"", AMERICAN JOURNAL OF MEDICAL GENETICS PART A, ss.2333-2334, 2011
dc.identifier.issn1552-4825
dc.identifier.othervv_1032021
dc.identifier.otherav_d92a759b-f5f7-43e9-a6c9-aaa4544f8418
dc.identifier.urihttp://hdl.handle.net/20.500.12627/143259
dc.identifier.urihttps://doi.org/10.1002/ajmg.a.34151
dc.language.isoeng
dc.subjectYaşam Bilimleri
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectTemel Bilimler
dc.subjectDahili Tıp Bilimleri
dc.subjectTıbbi Genetik
dc.subjectSağlık Bilimleri
dc.subjectTıp
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectGENETİK VE HAYAT
dc.titleResponse to Kouwenberg et al. "Recognizable Phenotype With Common Occurrence of Microcephaly, Psychomotor Retardation, But No Spontaneous Bone Fractures in ARCL2B Due to PYCR1 Mutations"
dc.typeMakale
dc.relation.journalAMERICAN JOURNAL OF MEDICAL GENETICS PART A
dc.contributor.departmentBoğaziçi Üniversitesi , ,
dc.identifier.issue9
dc.identifier.startpage2333
dc.identifier.endpage2334
dc.contributor.firstauthorID9834


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