M. Michael Cohen, Jr.: Author, diagnostician, geneticist, teacher, mentor, syndrome scholar extraordinaire (1937–2018)
dc.contributor.author | Carey, John C. | |
dc.contributor.author | Hennekam, Raoul C. M. | |
dc.contributor.author | Lin, Angela E. | |
dc.contributor.author | Barr, Mason | |
dc.date.accessioned | 2018-09-04T20:08:14Z | |
dc.date.available | 2019-09-04T20:15:40Z | en |
dc.date.issued | 2018-08 | |
dc.identifier.citation | Carey, John C.; Hennekam, Raoul C. M.; Lin, Angela E.; Barr, Mason (2018). "M. Michael Cohen, Jr.: Author, diagnostician, geneticist, teacher, mentor, syndrome scholar extraordinaire (1937–2018)." American Journal of Medical Genetics Part A 176(8): 1703-1705. | |
dc.identifier.issn | 1552-4825 | |
dc.identifier.issn | 1552-4833 | |
dc.identifier.uri | https://hdl.handle.net/2027.42/145521 | |
dc.publisher | Oxford University Press | |
dc.publisher | Wiley Periodicals, Inc. | |
dc.title | M. Michael Cohen, Jr.: Author, diagnostician, geneticist, teacher, mentor, syndrome scholar extraordinaire (1937–2018) | |
dc.type | Article | en_US |
dc.rights.robots | IndexNoFollow | |
dc.subject.hlbsecondlevel | Genetics | |
dc.subject.hlbtoplevel | Health Sciences | |
dc.description.peerreviewed | Peer Reviewed | |
dc.description.bitstreamurl | https://deepblue.lib.umich.edu/bitstream/2027.42/145521/1/ajmga38845.pdf | |
dc.description.bitstreamurl | https://deepblue.lib.umich.edu/bitstream/2027.42/145521/2/ajmga38845_am.pdf | |
dc.identifier.doi | 10.1002/ajmg.a.38845 | |
dc.identifier.source | American Journal of Medical Genetics Part A | |
dc.identifier.citedreference | Gorlin, R. J., Pindborg, J. J., & Cohen, M. M. Jr. ( 1976 ). Syndromes of the head and neck ( 2nd ed.). New York, NY: McGraw Hill. | |
dc.identifier.citedreference | Carey, J. C., & Erickson, R. P. ( 2007 ). Introductory comments: M. Michael Cohen, Jr. Festschrift. American Journal of Medical Genetics Part A, 143A ( 24 ), 2851 – 2852. | |
dc.identifier.citedreference | Carey, J. C., & Hall, B. D. ( 1978 ). Confirmation of the Cohen syndrome. Journal of Pediatrics, 93 ( 2 ), 239 – 244. | |
dc.identifier.citedreference | Cohen, M. M. Jr. ( 1979 ). Craniofrontonasal dysplasia. Birth Defects Original Article Series, 15 ( 5B ), 85 – 89. | |
dc.identifier.citedreference | Cohen, M. M. Jr. ( 1988 ). Further diagnostic thoughts about the Elephant Man. American Journal of Medical Genetics, 29 ( 4 ), 777 – 782. | |
dc.identifier.citedreference | Cohen, M. M. Jr. ( 2006 ). Perspectives on the face. New York, NY: Oxford University Press. | |
dc.identifier.citedreference | Cohen, M. M. Jr., Hall, B. D., Smith, D. W., Graham, C. B., & Lampert, K. J. ( 1973 ). A new syndrome with hypotonia, obesity, mental deficiency and facial, oral, ocular and limb anomalies. The Journal of Pediatrics, 83 ( 2 ), 280 – 284. | |
dc.identifier.citedreference | Cohen, M. M. Jr., & Hayden, P. W. ( 1979 ). A newly recognized hamartomatous syndrome. Birth Defects Original Article Series, 15 ( 5B ), 291 – 296. | |
dc.identifier.citedreference | Cohen, M. M. Jr. ( 1997 ). The child with multiple birth defects ( 2nd ed. ). New York, NY: Oxford University Press. | |
dc.identifier.citedreference | Cohen, M. M. Jr., Neri, G., & Weksberg, R. ( 2002 ). Overgrowth syndromes. New York, NY: Oxford University Press. | |
dc.identifier.citedreference | Gibson, W. T., Hood, R. L., Zhan, S. H., Bulman, D. E., Fejes, A. P., Moore, R. …., Jones, S. J. ( 2012 ). Mutations in EZH2 cause Weaver Syndrome. American Journal of Human Genetics, 90, 110 – 118. | |
dc.identifier.citedreference | Kolehmainen, J., Black, G. C. M., Saarinen, A., Chandler, K., Clayton‐Smith, J., Träskelin, A.‐L., … Lehesjoki, A.‐E. ( 2003 ). Cohen syndrome is caused by mutations in a novel gene, COH1, encoding a transmembrane protein with a presumed role in vesicle‐mediated sorting and intracellular protein transport. American Journal of Human Genetics, 72 ( 6 ), 1359 – 1369. | |
dc.identifier.citedreference | Weaver, D. D., Graham, C. B., Thomas, I. T., & Smith, D. W. ( 1974 ). A new overgrowth syndrome with accelerated skeletal maturation, unusual facies, and camptodactyly. The Journal of Pediatrics, 84 ( 4 ), 547 – 552. | |
dc.identifier.citedreference | Wiedemann, H. R., Burgio, G. R., Aldenhoff, P., Kunze, J., Kaufmann, H. J., & Schirg, E. ( 1983 ). The Proteus syndrome: Partial gigantism of the hands and feet, nevi, hemihypertrophy, subcutaneous tumors, macrocephaly or other skull anomalies and possible accelerated growth and visceral affections. European Journal of Pediatrics, 140, 5 – 12. | |
dc.owningcollname | Interdisciplinary and Peer-Reviewed |
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