View Item 

Show simple item record

Albumin cayemite: A Negro plasma albumin variant
dc.contributor.authorBasu, A.en_US
dc.contributor.authorWeitkamp, Lowell R.en_US
dc.contributor.authorGall, John C.en_US
dc.contributor.authorBrown, W.en_US
dc.date.accessioned2006-09-11T19:11:33Z
dc.date.available2006-09-11T19:11:33Z
dc.date.issued1969-06en_US
dc.identifier.citationWeitkamp, L. R.; Basu, A.; Gall, J. C.; Brown, W.; (1969). "Albumin cayemite: A Negro plasma albumin variant." Human Genetics 7(2): 180-182. <http://hdl.handle.net/2027.42/47614>en_US
dc.identifier.issn1432-1203en_US
dc.identifier.issn0340-6717en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/47614
dc.description.abstractAn inherited variant of human serum albumin has been found in a Negro family from Haiti. The variant is electrophoretically distinguishable from ten different previously reported types of albumin variants.en_US
dc.format.extent191642 bytes
dc.format.extent3115 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherSpringer-Verlagen_US
dc.subject.otherBiomedicineen_US
dc.subject.otherHuman Geneticsen_US
dc.subject.otherMolecular Medicineen_US
dc.subject.otherInternal Medicineen_US
dc.subject.otherMetabolic Diseasesen_US
dc.titleAlbumin cayemite: A Negro plasma albumin varianten_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelMolecular, Cellular and Developmental Biologyen_US
dc.subject.hlbsecondlevelGeneticsen_US
dc.subject.hlbsecondlevelBiological Chemistryen_US
dc.subject.hlbtoplevelScienceen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Human Genetics, University of Michigan Medical School, Ann arbor, USA; Department of Anatomy, University of North Carolina Medical School, Chapel Hill, USA; Department of Pediatrics, University of Michigan Medical School, Ann arbor, USAen_US
dc.contributor.affiliationumDepartment of Human Genetics, University of Michigan Medical School, Ann arbor, USA; Department of Anatomy, University of North Carolina Medical School, Chapel Hill, USA; Department of Pediatrics, University of Michigan Medical School, Ann arbor, USAen_US
dc.contributor.affiliationumDepartment of Human Genetics, University of Michigan Medical School, Ann arbor, USA; Department of Anatomy, University of North Carolina Medical School, Chapel Hill, USA; Department of Pediatrics, University of Michigan Medical School, Ann arbor, USAen_US
dc.contributor.affiliationumDepartment of Human Genetics, University of Michigan Medical School, Ann arbor, USA; Department of Anatomy, University of North Carolina Medical School, Chapel Hill, USA; Department of Pediatrics, University of Michigan Medical School, Ann arbor, USAen_US
dc.contributor.affiliationumcampusAnn Arboren_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/47614/1/439_2004_Article_BF00287083.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1007/BF00287083en_US
dc.identifier.sourceHuman Geneticsen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


Files in this item

Name:
439_2004_Article_BF00287083.pdf
Size:
187.1KB
Format:
PDF
View/Open

Show simple item record

Remediation of Harmful Language

The University of Michigan Library aims to describe its collections in a way that respects the people and communities who create, use, and are represented in them. We encourage you to Contact Us anonymously if you encounter harmful or problematic language in catalog records or finding aids. More information about our policies and practices is available 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.