View Item 

Show simple item record

Autosomal recessive alobar holoprosencephaly with essentially normal faces
dc.contributor.authorBarr, Masonen_US
dc.contributor.authorCohen, M. Michaelen_US
dc.date.accessioned2006-04-19T13:44:40Z
dc.date.available2006-04-19T13:44:40Z
dc.date.issued2002-09-15en_US
dc.identifier.citationBarr, Mason; Cohen, M. Michael (2002)."Autosomal recessive alobar holoprosencephaly with essentially normal faces." American Journal of Medical Genetics 112(1): 28-30. <http://hdl.handle.net/2027.42/34663>en_US
dc.identifier.issn0148-7299en_US
dc.identifier.issn1096-8628en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/34663
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=12239716&dopt=citationen_US
dc.description.abstractHoloprosencephaly is associated with a diagnostic face approximately 80% of the time. We report three siblings with alobar holoprosencephaly and essentially normal faces. A similar family was reported by Khan et al. [1970: Dev Med Child Neurol 12:71–76]. Alobar holoprosencephaly with essentially normal faces has also been observed in infants of diabetic mothers [Barr et al., 1983 : J Pediatr 102:565–568]. © 2002 Wiley-Liss, Inc.en_US
dc.format.extent91767 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherWiley Subscription Services, Inc., A Wiley Companyen_US
dc.subject.otherLife and Medical Sciencesen_US
dc.subject.otherGeneticsen_US
dc.titleAutosomal recessive alobar holoprosencephaly with essentially normal facesen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelGeneticsen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.subject.hlbtoplevelScienceen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartments of Pediatrics, Pathology, and Obstetrics, University of Michigan, Ann Arbor, Michigan ; University of Michigan Hospitals, 1924 Taubman Center, Box 0318, Ann Arbor, Michigan 48109.en_US
dc.contributor.affiliationotherDepartments of Oral and Maxillofacial Sciences, Pediatrics, Community Health and Epidemiology, Health Services Administration, and Sociology and Social Anthropology, Dalhousie University, Halifax, Nova Scotia, Canadaen_US
dc.identifier.pmid12239716en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/34663/1/10587_ftp.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1002/ajmg.10587en_US
dc.identifier.sourceAmerican Journal of Medical Geneticsen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


Files in this item

Name:
10587_ftp.pdf
Size:
89.61KB
Format:
PDF
View/Open

Show simple item record

Remediation of Harmful Language

The University of Michigan Library aims to describe library materials in a way that respects the people and communities who create, use, and are represented in our collections. Report harmful or offensive language in catalog records, finding aids, or elsewhere in our collections anonymously through our metadata feedback form. More information at Remediation of Harmful Language.

Accessibility

If you are unable to use this file in its current format, please select the Contact Us link and we can modify it to make it more accessible to you.