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REFERENCES

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  • Cohen MM Jr. 1979. Craniofrontonasal dysplasia. Birth Defects 15: 8589.
  • Cohen MM Jr. 1982. The child with multiple birth defects, 1st edition. New York: Raven Press.
  • Cohen MM Jr. 1987a. Noses nobody knows. Proc Greenwood Genet Ctr 6: 183184.
  • Cohen MM Jr. 1987b. The elephant man did not have neurofibromatosis (presented in 1986). Proc Greenwood Genet Ctr 6: 187192.
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  • Cohen MM Jr. 1988b. Understanding Proteus syndrome, unmasking the elephant man, and stemming elephant fever. Neurofibromatosis 1: 260280.
  • Cohen MM Jr. 1995. Letter to the Editor: Will the real ophthalmologist please stand up? Am J Med Genet 56: 425.
  • Cohen MM Jr. 1997. M. Michael Cohen Sr., 1905–1995: A remembrance. In: MM, CohenJr BaumBJ, editors. Studies in Stomatology and Craniofacial Biology. Amsterdam: IOS Press. pp. 716.
  • Cohen MM Jr. 2005. Proteus syndrome: An update. Am J Med Genet Part C Semin Med Genet 137C: 3852.
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  • Cohen MM Jr. 2007a. Robert J. Gorlin, 1923–2006: Evolution of his phenotype. Am J Hum Genet 80: 585587.
  • Cohen MM Jr. 2007b. Robert J. Gorlin as a humorist. Am J Med Genet Part A 143A: 11311134.
  • Cohen MM Jr, Hayden PW. 1979. A newly recognized hamartomatous syndrome. Birth Defects 15: 291296.
  • CohenMMJr, RollnickBR, editors. 1985. Craniofacial dysmorphology: Studies in honor of Samuel Pruzansky. New York: Alan R. Liss, Inc.
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  • Cohen MM Jr, Hall BD, Smith DW, Graham CB, Lampert KJ. 1973. A new syndrome with hypotonia, obesity, mental deficiency, and facial, oral, ocular, and limb anomalies. J Pediatr 83: 280284.
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  • Jirasek JE. In: CohenMMJr. 1971. Development of the Genital System and Male Pseudohermaphroditism. Baltimore: Johns Hopkins University Press.
  • Kolehmainen J, Black GCM, Saarinen A, Chandler K, Clayton-Smith J, Träskelin A-L, Perveen R, Kivitie-Kallio S, Norio R, Warburg M, Fryns J-P, de la Chapelle A, 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. Am J Hum Genet 72: 13591369.
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  • Mulliken JB. 1975. Samuel prescott: Physician-patriot. Arch Surg 110: 375376.
  • OMIM 608763. 2008. Ehlers-Danlos syndrome, Beasley-Cohen type.
  • OMIM 216550 607817. 2008. Cohen syndrome, COH1 gene.
  • Shepard TH, Lemire RJ. 2007. Catalog of Teratogenic Agents, 12th edition. Baltimore: John Hopkins University Press.
  • Siebert JR, Cohen MM Jr, Sulik KK, Shaw C-M, Lemire RJ. 1990. Holoprosencephaly: An Overview and Atlas of Cases. New York: Wiley-Liss.
  • Tibbles JAR, Cohen MM Jr. 1986. Proteus syndrome: The elephant man diagnosed (Cohen, corresponding author). Brit Med J 293: 683685.
  • Twigg SRF, Kan B, Babbs C, Bochukova EG, Robertson SP, Wall SA, Morriss-Kay GM, Wilkie AOM. 2004. Mutations of ephrin-B1 (EFNB1), a marker of tissue boundary formation, cause craniofrontonasal syndrome. Proc Natl Acad Sci 101: 86528657.
  • Vinay S, Andreas R, Bernhard ZW, Gerhardt S. 2000. Gorlin-Cohen syndrome. J Foot Ankle Surg 39: 131135.
  • Warkany J, Lemire RE, Cohen MM Jr. 1981. Mental Retardation and Congenital Malformations of the Central Nervous System. Chicago: Yearbook Medical Publishers, Inc.
  • Weinmann JP, Sicher H. 1955. Bones and Bones: Fundamentals of Bone Biology. St. Louis: C. V. Mosby Co.
  • Wiedemann H-R, Burgio GR, Aldenhoff P, Kunze J, Kaufman HJ, Schirg E. 1983. The Proteus syndrome, partial gigantism of the hands and/or feet, nevi, hemihypertrophy, subcutaneous tumors, macrocephaly, skull anomalies, possible accelerated growth and visceral affections. Eur J Pediatr 140: 512.
  • Willis RA. 1962. The Borderland between Embryology and Pathology. London: Butterworths.