View Item 

Show simple item record

M. Michael Cohen, Jr.: Author, diagnostician, geneticist, teacher, mentor, syndrome scholar extraordinaire (1937–2018)
dc.contributor.authorCarey, John C.
dc.contributor.authorHennekam, Raoul C. M.
dc.contributor.authorLin, Angela E.
dc.contributor.authorBarr, Mason
dc.date.accessioned2018-09-04T20:08:14Z
dc.date.available2019-09-04T20:15:40Zen
dc.date.issued2018-08
dc.identifier.citationCarey, 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.issn1552-4825
dc.identifier.issn1552-4833
dc.identifier.urihttps://hdl.handle.net/2027.42/145521
dc.publisherOxford University Press
dc.publisherWiley Periodicals, Inc.
dc.titleM. Michael Cohen, Jr.: Author, diagnostician, geneticist, teacher, mentor, syndrome scholar extraordinaire (1937–2018)
dc.typeArticleen_US
dc.rights.robotsIndexNoFollow
dc.subject.hlbsecondlevelGenetics
dc.subject.hlbtoplevelHealth Sciences
dc.description.peerreviewedPeer Reviewed
dc.description.bitstreamurlhttps://deepblue.lib.umich.edu/bitstream/2027.42/145521/1/ajmga38845.pdf
dc.description.bitstreamurlhttps://deepblue.lib.umich.edu/bitstream/2027.42/145521/2/ajmga38845_am.pdf
dc.identifier.doi10.1002/ajmg.a.38845
dc.identifier.sourceAmerican Journal of Medical Genetics Part A
dc.identifier.citedreferenceGorlin, 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.citedreferenceCarey, 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.citedreferenceCarey, J. C., & Hall, B. D. ( 1978 ). Confirmation of the Cohen syndrome. Journal of Pediatrics, 93 ( 2 ), 239 – 244.
dc.identifier.citedreferenceCohen, M. M. Jr. ( 1979 ). Craniofrontonasal dysplasia. Birth Defects Original Article Series, 15 ( 5B ), 85 – 89.
dc.identifier.citedreferenceCohen, M. M. Jr. ( 1988 ). Further diagnostic thoughts about the Elephant Man. American Journal of Medical Genetics, 29 ( 4 ), 777 – 782.
dc.identifier.citedreferenceCohen, M. M. Jr. ( 2006 ). Perspectives on the face. New York, NY: Oxford University Press.
dc.identifier.citedreferenceCohen, 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.citedreferenceCohen, M. M. Jr., & Hayden, P. W. ( 1979 ). A newly recognized hamartomatous syndrome. Birth Defects Original Article Series, 15 ( 5B ), 291 – 296.
dc.identifier.citedreferenceCohen, M. M. Jr. ( 1997 ). The child with multiple birth defects ( 2nd ed. ). New York, NY: Oxford University Press.
dc.identifier.citedreferenceCohen, M. M. Jr., Neri, G., & Weksberg, R. ( 2002 ). Overgrowth syndromes. New York, NY: Oxford University Press.
dc.identifier.citedreferenceGibson, 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.citedreferenceKolehmainen, 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.citedreferenceWeaver, 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.citedreferenceWiedemann, 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.owningcollnameInterdisciplinary and Peer-Reviewed


Files in this item

Name:
ajmga38845.pdf
Size:
2.965MB
Format:
PDF
View/Open
Name:
ajmga38845_am.pdf
Size:
185.2KB
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.