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Holoprosencephaly anomaly with nasal and premaxillar agenesis (possibly autosomal recessive type).

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dc.contributor.authorAydoğdu, Sultan Durmuş
dc.contributor.authorAysun Yakut
dc.contributor.authorÖner Ünsal
dc.contributor.authorM. Arif Aksit
dc.contributor.authorN Tel
dc.contributor.orcid0000-0001-7792-8438
dc.contributor.orcid0000-0001-7562-6727
dc.date.accessioned2025-11-13T20:53:30Z
dc.date.issued1994-07-26
dc.identifier.endpage62
dc.identifier.issue2
dc.identifier.openalexW2395367400
dc.identifier.startpage157
dc.identifier.urihttps://hdl.handle.net/11421/12905
dc.identifier.urihttps://pubmed.ncbi.nlm.nih.gov/8016918
dc.identifier.volume36
dc.language.isoen
dc.relation.ispartofPubMed
dc.rightsrestrictedAccess
dc.subjectHoloprosencephaly
dc.subjectMicrophthalmia
dc.subjectMedicine
dc.subjectAnatomy
dc.subjectMicrocephaly
dc.subjectCerebrum
dc.subjectSkull
dc.subjectAgenesis of the corpus callosum
dc.subjectCorpus Callosum Agenesis
dc.subjectNose
dc.subjectAgenesis
dc.subjectNasal septum
dc.subjectCorpus callosum
dc.subjectFetus
dc.subjectCentral nervous system
dc.subjectBiology
dc.subjectPregnancy
dc.subjectInternal medicine
dc.subjectGenetics
dc.subject.sdg14
dc.titleHoloprosencephaly anomaly with nasal and premaxillar agenesis (possibly autosomal recessive type).
dc.typeArticle
dspace.entity.typePublication
local.authorid.openalexA5064565873

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