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- W1992163977 abstract "American Journal of Medical GeneticsVolume 30, Issue 4 p. 939-942 Invited Editorial Comment Chance vs. Causality in the association of Down syndrome and holoprosencephaly Dr. Charles J. Epstein, Corresponding Author Dr. Charles J. Epstein Department of Pediatrics, University of California, San Francisco, CaliforniaDepartment of Pediatrics, University of California, San Francisco, CA 94143-0106Search for more papers by this authorSusan Seto, Susan Seto Department of Pediatrics, University of California, San Francisco, CaliforniaSearch for more papers by this authorMahin Golabi, Mahin Golabi Department of Pediatrics, University of California, San Francisco, CaliforniaSearch for more papers by this author Dr. Charles J. Epstein, Corresponding Author Dr. Charles J. Epstein Department of Pediatrics, University of California, San Francisco, CaliforniaDepartment of Pediatrics, University of California, San Francisco, CA 94143-0106Search for more papers by this authorSusan Seto, Susan Seto Department of Pediatrics, University of California, San Francisco, CaliforniaSearch for more papers by this authorMahin Golabi, Mahin Golabi Department of Pediatrics, University of California, San Francisco, CaliforniaSearch for more papers by this author First published: August 1988 https://doi.org/10.1002/ajmg.1320300410Citations: 15AboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onEmailFacebookTwitterLinkedInRedditWechat References Aronson DC, Jansweijer MCE, Hoovers JMN, Barth PG (1987): A male infant with holoprosencephaly associated with ring chromosome 21. Clin Genet 31: 48–52. Barr M Jr, Hanson JW, Currey K, Sharp S, Toriello H, Schmickel RD, Wilson G (1983): Holoprosencephaly in infants of diabetic mothers. J Pediatr 102: 565–568. Epstein, CJ (1986): “ The Consequences of Chromosome Imbalance. Principles, Mechanisms, and Models.” New York: Cambridge University Press. Epstein, CJ (1988): Invited editorial comment: Specificity versus nonspecificity in the pathogenesis of aneuploid phenotypes. Am J Med Genet 29: 161–165. Estabrooks LL, Rao KW, Seeds JW, Donahue RP, Aylsworth AS (1987): Nonsyndromic holoprosencephaly in an infant with a minute deletion of chromosome 21(q22.3). Am J Hum Genet 41: A118. Opitz JM (1986): Editorial comment: Developmental field theory and observations—accidental progress? Am J Med Genet Suppl 2: 1–8. Pi S-Y, Fineman RM, Wing SD, Grunnet M, Chan G (1980): Holoprosencephaly in a Down syndrome child. Am J Med Genet 5: 201–206. Shapiro B (1970): Prental dental anomalies in mongolism: comments on the basis and implications of variability. Ann NY Acad Sci 171 (2): 562–577. Shapiro B (1983): Down syndrome—a disruption of homeostasis. Am J Med Genet 14: 241–270. Urioste M, Valcarcel E, Gomez MA, Pinel I, Garcia de León R, Diaz de Bustamante A, Tebar R, Martinez-Frias ML (1988): Holoprosencephaly and trisomy 21 in a child born to a nondiabetic mother. Am J Med Genet 30: 925–928. U. S. Bureau of the Census (1986): “ Statistical Abstract of the United States: 1987” (107th ed.). Washington, D. C. Citing Literature Volume30, Issue4August 1988Pages 939-942 ReferencesRelatedInformation" @default.
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- W1992163977 title "Chance vs. Causality in the association of Down syndrome and holoprosencephaly" @default.
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