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Clinical and genetic investigations of families with pure benign familial infantile convulsions (BFIC): Confirmation of linkage to chromosome 16

dc.contributor.authorRating, D
dc.contributor.authorWeber, YG
dc.contributor.authorBerger, A
dc.contributor.authorKarafyllakes, S
dc.contributor.authorMaier, S
dc.contributor.authorKurlemann, G
dc.contributor.authorPust, B
dc.contributor.authorHalbach, A
dc.contributor.authorLaux, C
dc.contributor.authorStephani, U
dc.contributor.authorFukuyama, Y
dc.contributor.authorOsawa, M
dc.contributor.authorSaito, K
dc.contributor.authorLehmann-Hom, F
dc.contributor.authorJurkat-Rott, K
dc.contributor.authorLerche, H
dc.contributor.authorNeubauer, B
dc.contributor.authorBebek, Nerses
dc.date.accessioned2021-03-06T11:13:54Z
dc.date.available2021-03-06T11:13:54Z
dc.identifier.citationWeber Y., Bebek N., Berger A., Karafyllakes S., Maier S., Kurlemann G., Rating D., Pust B., Halbach A., Laux C., et al., "Clinical and genetic investigations of families with pure benign familial infantile convulsions (BFIC): Confirmation of linkage to chromosome 16", 25th International Epilepsy Congress, Lisbon, Portekiz, 12 - 16 Ekim 2003, cilt.44, ss.166
dc.identifier.otherav_ee0f0ade-9d11-4195-b8e4-1a3195c6e144
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/156291
dc.language.isoeng
dc.subjectNeurology (clinical)
dc.subjectHealth Sciences
dc.subjectLife Sciences
dc.subjectKLİNİK NEUROLOJİ
dc.subjectKlinik Tıp
dc.subjectKlinik Tıp (MED)
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectNöroloji
dc.subjectNeurology
dc.titleClinical and genetic investigations of families with pure benign familial infantile convulsions (BFIC): Confirmation of linkage to chromosome 16
dc.typeBildiri
dc.contributor.department, ,
dc.identifier.volume44
dc.contributor.firstauthorID128410


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