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• W2007294007 abstract "American Journal of Medical GeneticsVolume 47, Issue 5 p. 687-688 Editorial Comment Developmental field theory and the molecular analysis of morphogenesis: A comment on Dr. Slavkin's observations John M. Opitz, Corresponding Author John M. Opitz Shodair Hospital, Helena and Montana State University, Bozeman, Montana Universities of Washington/ Seattle and Wisconsin/MadisonShodair Hospital, Box 5539, Helena, MT 59604Search for more papers by this authorScott F. Gilbert, Scott F. Gilbert Martin Biological Labs, Department of Biology, Swarthmore College, Swarthmore, PennsylvaniaSearch for more papers by this author John M. Opitz, Corresponding Author John M. Opitz Shodair Hospital, Helena and Montana State University, Bozeman, Montana Universities of Washington/ Seattle and Wisconsin/MadisonShodair Hospital, Box 5539, Helena, MT 59604Search for more papers by this authorScott F. Gilbert, Scott F. Gilbert Martin Biological Labs, Department of Biology, Swarthmore College, Swarthmore, PennsylvaniaSearch for more papers by this author First published: 1 October 1993 https://doi.org/10.1002/ajmg.1320470520Citations: 9AboutPDF 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 No abstract is available for this article. References Arn PH, Mankinen C, Jabs EW (1993): Mild mandibulofacial dysost-osis in a child with a deletion of 3p. Am J Med Genet 46: 534–536. Coelho CND, Upholt WB, Kosher RA (1993): The expression pattern of the chicken homeobox-containing gene GHox-7 in developing poly-dactylous limb buds suggests its involvement in apical ectodermal ridge-directed outgrowth of limb mesoderm and in programmed cell death. Different 52: 129–137. De Robertis EM, Morita EA, Cho KWY (1991): Gradient fields and homeobox genes. Development 112: 669–678. Gilbert SF (1993): Cellular dialogues during organogenesis. Program and Abstracts, III Int. Workshop on Fetal Genetic Pathol., Perugia Bosco, June, 1993. Proceedings in preparation. Gorlin RJ, Cohen MM Jr, Levin LS (1990): “ Syndromes of the Head and Neck,” 3rd ed. New York: Oxford University Press, pp 859–861, Rieger syndrome. Graham A, Lumsden A (1993): The role of segmentation in the development of the branchial region of higher vertebrate embryos. In: JM Opitz (ed): “ Blastogenesis, Normal and Abnormal.” New York, Wiley-Liss/March of Dimes Birth Defects Foundation BD:OAS XXIX: 99–108, in press. Jowett AK, Vainio S, Ferguson MWJ, Sharpe PT, Thesleff I (1993): Epithelial-mesenchymal interactions are responsible for msx 1 and msx 2 gene expression in the developing murine molar tooth. Development 117: 461–470. Lowenstein EJ, Daly RJ, Batzer AG, Li W, Margolis B, Lammers R, Ullrich A, Skolnik EY, Bar-Sagi D, Schlessinger J (1992): The SH2 and SH3 domain-containing protein GRB2 links receptor tyrosine kinases to ras signaling. Cell 70: 431–442. MacKenzie A, Leening GL, Jowett AK, Ferguson MWJ, Sharpe PT (1991): The homeobox gene 7.1 has specific regional and temporal patterns during early murine craniofacial embryogenesis, especially tooth development in vivo and in vitro. Development 111: 269–285. Mann GB, Fowler KJ, Gabriel A, Nice EC, Williams RL, Dunn AR (1993): Mice with a null mutation of the TGFα gene have abnormal skin architecture, wavy hair, and curly whiskers and often develop corneal inflammation. Cell 73: 249–261. Monaghan AP, Hill RE, Bhattacharya SS, Graham EE, Davidson DR (1991): Msh-Mke homoebox genes in the developing vertebrate eye. Development 112: 1053–1061. Opitz JM (1993): Blastogenesis and the “primary field” in human development. In: JM Opitz (ed): “ Blastogenesis, Normal and Abnormal.” New York, Wiley-Liss/March of Dimes Birth Defects Foundation BD:OAS XXIX: 99–108, 1–34, in press. Opitz JM, Mollica F, Sorge G, Milana G, Cimino G (1993): Acrofacial dysostoses: Review and report of a previously undescribed condition: The autosomal or X-linked dominant Catania form of acrofacial dysostosis. Am J Med Genet 47: 660–678. Ritvos O, Tuuri T, Erämaa M, Sainio K, Hildén K, Saxén L, Gilbert SF (1993): Activin disrupts epithelial branching morphogenesis in developing glandular organs of the mouse. Manuscript submitted. Simon MA, Dodson GS, Rubin GM (1993): An SH3-SH2-SH3 protein is required for p21ras1 activation and binds to sevenless and Sos proteins in vitro. Cell 73: 169–177. Slavkin HD (1993): Rieger syndrome revisited: Experimental approaches using pharmacologic and antisense strategies to abrogate EGF and TGF-α functions resulting in dysmorphogenesis during embryonic mouse craniofacial morphogenesis. Am J Med Genet 47: 689–697. Vassar R, Fuchs E (1991): Transgenic mice provide new insights into the role of TGF-α during epidermal development and differentiation. Genes Dev 5: 714–727. Citing Literature Volume47, Issue51 October 1993Pages 687-688 ReferencesRelatedInformation" @default.
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