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Roberts syndrome-SC phocomeliia: Clinical and molecular findings

dc.contributor.authorJabs, E. W.
dc.contributor.authorZou, H.
dc.contributor.authorGordillo, M.
dc.contributor.authorVega, H.
dc.contributor.authorHou, F.
dc.contributor.authorJoenje, H.
dc.contributor.authorWaisfisz, Q.
dc.contributor.authorChang, S.
dc.contributor.authorPaznekas, W. A.
dc.contributor.authorManouvrier, S.
dc.contributor.authorSchnur, R.
dc.contributor.authorUzielli, M.
dc.contributor.authorHennekam, R.
dc.contributor.authorSkovby, F.
dc.contributor.authorKayserili, H.
dc.contributor.authorLuque, R.
dc.contributor.authorTrainer, A.
dc.date.accessioned2021-03-05T12:39:32Z
dc.date.available2021-03-05T12:39:32Z
dc.identifier.citationVega H., Jabs E. W. , Gordillo M., Trainer A., Luque R., Kayserili H., Skovby F., Hennekam R., Uzielli M., Schnur R., et al., "Roberts syndrome-SC phocomeliia: Clinical and molecular findings", 2nd National Scientific Symposium held in Conjunction with the Cornelia-de-Lange-Syndrome-Foundation 25th National Meeting, Connecticut, Amerika Birleşik Devletleri, 22 Haziran 2006, ss.1298-1299
dc.identifier.otherav_ae3ed499-e09c-45f6-a87d-d27fdbfee513
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/116257
dc.language.isoeng
dc.subjectTemel Bilimler
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectYaşam Bilimleri
dc.subjectTıbbi Genetik
dc.subjectDahili Tıp Bilimleri
dc.subjectSağlık Bilimleri
dc.subjectTıp
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectGENETİK VE HAYAT
dc.titleRoberts syndrome-SC phocomeliia: Clinical and molecular findings
dc.typeBildiri
dc.contributor.department, ,
dc.contributor.firstauthorID133994


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