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Inherited pericentric inversion of chromosome number two: A linkage study *
dc.contributor.authorWeitkamp, Lowell R.en_US
dc.contributor.authorJanzen, M. K.en_US
dc.contributor.authorGuttormsen, S. A.en_US
dc.contributor.authorGershowitz, Henryen_US
dc.date.accessioned2010-04-01T15:42:53Z
dc.date.available2010-04-01T15:42:53Z
dc.date.issued1969-07en_US
dc.identifier.citationWEITKAMP, L. R.; JANZEN, M. K.; GUTTORMSEN, S. A.; GERSHOWITZ, H. (1969). "Inherited pericentric inversion of chromosome number two: A linkage study * ." Annals of Human Genetics 33(1): 53-59. <http://hdl.handle.net/2027.42/66205>en_US
dc.identifier.issn0003-4800en_US
dc.identifier.issn1469-1809en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/66205
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=5367461&dopt=citationen_US
dc.format.extent720627 bytes
dc.format.extent3110 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.publisherBlackwell Publishing Ltden_US
dc.rights1969 University College London and Blackwell Publishing Ltden_US
dc.titleInherited pericentric inversion of chromosome number two: A linkage study *en_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelGeneticsen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Human Genetics, University of Michigan Medical School, Ann Arbor, Michiganen_US
dc.identifier.pmid5367461en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/66205/1/j.1469-1809.1969.tb01629.x.pdf
dc.identifier.doi10.1111/j.1469-1809.1969.tb01629.xen_US
dc.identifier.sourceAnnals of Human Geneticsen_US
dc.identifier.citedreferenceCarr, D. H. ( 1962 ) Chromosome anomalies with special reference to Klinefelter's syndrome. Trans. Am. Ass. Geneto.-Urin. Surg. 54, 9.en_US
dc.identifier.citedreferenceCohen, M. M., Capparo, V. J. & Tokagi, N. ( 1967 ) Pericentric inversion in a group D chromosome (13–15) associated with amenorrhoea and gonadal dysgenesis. Ann. Hum. Genet., Lond. 30, 313.en_US
dc.identifier.citedreferenceDeGrouchy, J., Emerit, I., Corone, P., Vernant, P., Lamy, M. & Soulie, P. ( 1963 ) Inversion pÉricentric probable du chromosome no. 2 et malformations congÉnitales chez un garÇon. Annls GÉnÉt. 6, 21.en_US
dc.identifier.citedreferenceHaldane, J. B. S. & Smith, C. A. B. ( 1947 ) A new estimate of the linkage between genes for colour-blindness and haemophilia in man. Ann. Eugen. 14, 10.en_US
dc.identifier.citedreferenceJacobs, P. A., Cruickshank, G., Faed, M. J. W., Frackiewicz, A., Robson, E. B., Harris, H. & Sutherland, I. ( 1967 ) Pericentric inversion of a group C autosome: a study of three families. Ann. Hum. Genet., Lond. 31, 219.en_US
dc.identifier.citedreferenceMoorehead, P. S., Nowell, P. C., Mellman, W. J., Buttips, D. M., & Hungerford, D. A. ( 1960 ) Chromosome preparations of leukocytes cultured from human peripheral blood. Expl Cell Res. 20, 613.en_US
dc.identifier.citedreferenceNance, W. E. & Engel, E. ( 1967 ) Human cytogenetics: a brief review and presentation of new findings. J. Bone Jt Surg. 49-A, 1436.en_US
dc.identifier.citedreferenceSchmid, W. ( 1967 ) Pericentric inversions. J. GÉnÉt. hum. 16, 89.en_US
dc.identifier.citedreferenceSmith, C. A. B. ( 1959 ) Some comments on the statistical methods used in linkage investigations. Am. J. Hum. Genet. 11, 289.en_US
dc.identifier.citedreferenceSoudek, D., LaxovÁ, R. & AdÁmek, R. ( 1968 ) Pericentric inversion in a family with a 21/22 translocation. Cytogenet. 7, 108.en_US
dc.identifier.citedreferenceSummitt, R. L. & Atnip, R. L. ( 1966 ) Chromosomal aberrations with normal phenotype: four examples. Ala. J. Med. Sci. 3, 483.en_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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