Molecular cytogenetic analysis of patients with holoprosencephaly and structural rearrangements of 7q

dc.contributor.authorVance, Gail H.
dc.contributor.authorNickerson, Catherine
dc.contributor.authorSarnat, Lauren
dc.contributor.authorZhang, Aiwu
dc.contributor.authorHenegariu, Octavian
dc.contributor.authorMorichon-Delvallez, Nicole
dc.contributor.authorButler, Merlin G.
dc.contributor.authorPalmer, Catherine G.
dc.contributor.departmentMedical and Molecular Genetics, School of Medicineen_US
dc.date.accessioned2020-02-26T14:01:46Z
dc.date.available2020-02-26T14:01:46Z
dc.date.issued1998-02-26
dc.description.abstractThe holoprosencephaly (HPE) sequence is a malformation complex with abnormal midline cleavage of the embryonic forebrain. HPE is genetically heterogeneous with at least 6 different chromosome regions containing genes involved in the expression of the phenotype. HPE3, recently identified as the human Sonic hedgehog gene, is localized to 7q36. We have used fluorescence in situ hybridization (FISH) and polymerase chain reaction (PCR) amplification in 5 cell lines from patients with HPE (3 cases), HPE and sacral agenesis (1 case), and microcephaly (1 case) to further define the structural rearrangements of the long arm of chromosome 7 in each case. All cell lines demonstrated loss of material in the critical region of HPE3 at band 7q36, which includes the Sonic hedgehog gene. We report here the analysis of these patient cell lines.en_US
dc.eprint.versionAuthor's manuscripten_US
dc.identifier.citationVance, G. H., Nickerson, C., Sarnat, L., Zhang, A., Henegariu, O., Morichon-Delvallez, N., Butler, M. G., & Palmer, C. G. (1998). Molecular cytogenetic analysis of patients with holoprosencephaly and structural rearrangements of 7q. American journal of medical genetics, 76(1), 51–57.en_US
dc.identifier.urihttps://hdl.handle.net/1805/22157
dc.language.isoen_USen_US
dc.publisherWileyen_US
dc.relation.journalAmerican Journal of Medical Geneticsen_US
dc.rightsPublisher Policyen_US
dc.sourcePMCen_US
dc.subjectHoloprosencephalyen_US
dc.subjectBrain malformationen_US
dc.subjectChromosome 7en_US
dc.subjectFluorescence in situ hybridizationen_US
dc.titleMolecular cytogenetic analysis of patients with holoprosencephaly and structural rearrangements of 7qen_US
dc.typeArticleen_US
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