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Patterson-Stevenson-Fontaine syndrome: 30-year follow-up and clinical details of a further affected case

1997; Wiley; Volume: 69; Issue: 4 Linguagem: Inglês

10.1002/(sici)1096-8628(19970414)69

1096-8628

Andrew O.M. Wilkie, Tim Goodacre,

Genetic and rare skin diseases.

American Journal of Medical GeneticsVolume 69, Issue 4 p. 433-434 Letter to the Editor Patterson-Stevenson-Fontaine syndrome: 30-year follow-up and clinical details of a further affected case Andrew O. M. Wilkie, Corresponding Author Andrew O. M. Wilkie awilkie @molbiol.ox.ac.uk Institute of Molecular Medicine, John Radcliffe Hospital, Headington, Oxford, UKInstitute of Molecular Medicine, John Radcliffe Hospital, Headington, Oxford OX3 9DU, UK.Search for more papers by this authorTimothy E. E. Goodacre, Timothy E. E. Goodacre Department of Plastic & Reconstructive Surgery, The Radcliffe Infirmary NHS Trust, Oxford, UKSearch for more papers by this author Andrew O. M. Wilkie, Corresponding Author Andrew O. M. Wilkie awilkie @molbiol.ox.ac.uk Institute of Molecular Medicine, John Radcliffe Hospital, Headington, Oxford, UKInstitute of Molecular Medicine, John Radcliffe Hospital, Headington, Oxford OX3 9DU, UK.Search for more papers by this authorTimothy E. E. Goodacre, Timothy E. E. Goodacre Department of Plastic & Reconstructive Surgery, The Radcliffe Infirmary NHS Trust, Oxford, UKSearch for more papers by this author First published: 06 December 1998 https://doi.org/10.1002/(SICI)1096-8628(19970414)69:4 3.0.CO;2-NCitations: 6AboutPDF 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 Crackower MA, Scherer SW, Rommens JM, Hui C-C, Poorkaj P, Soder S, Cobben JM, Hudgins L, Evans JP, Tsui L-C (1996): Characterization of the split hand/split foot malformation locus SHFM1 at 7q21.3–q22.1 and analysis of a candidate gene for its expression during limb development. Hum Mol Genet 5: 571–579. 10.1093/hmg/5.5.571 CASPubMedWeb of Science®Google Scholar Fontaine G, Farriaux JP, Delattre P, Gidlecki Z, Poupard B, Durieux G, Piquet JJ (1974): Une observation familiale du syndrome ectrodactylie et dysostose mandibulo-faciale. J Génét Hum 22: 289–307. CASPubMedWeb of Science®Google Scholar Jarvik GP, Patton MA, Homfray T, Evans JP (1994): Non-Mendelian transmission in a human developmental disorder: split hand/split foot. Am J Hum Genet 55: 710–713. PubMedWeb of Science®Google Scholar Johnson KR, Lane PW, Ward-Bailey P, Davisson MT (1995): Mapping the mouse dactylaplasia mutation, Dac, and a second gene that controls its expression, mdac. Genomics 29: 457–464. 10.1006/geno.1995.9981 CASPubMedWeb of Science®Google Scholar Nunes ME, Schutt G, Kapur RP, Luthardt F, Kukolich M, Byers P, Evans JP: (1995): A second autosomal split hand/split foot locus maps to chromosome 10q24–q25. Hum Mol Genet 4: 2165–2170. 10.1093/hmg/4.11.2165 CASPubMedWeb of Science®Google Scholar Opitz JM, Mollica F, Sorge G, Milana G, Cimino G, Caltabiano M (1993): Acrofacial dysostoses: review and report of a previously undescribed condition: the autosomal or X-linked dominant Catania form of acro-facial dysostosis. Am J Med Genet 47: 660–678. 10.1002/ajmg.1320470517 CASPubMedWeb of Science®Google Scholar Patterson TJS, Stevenson AC (1964): Cranio-facial dysostosis and malformations of feet. J Med Genet 1: 112–114. 10.1136/jmg.1.2.112 CASPubMedGoogle Scholar Stevenson AC, Jennings LM (1960): Ectrodactyly—evidence in favour of a disturbed segregation in the offspring of affected males. Ann Hum Genet 24: 89–96. 10.1111/j.1469-1809.1959.tb01719.x CASPubMedWeb of Science®Google Scholar Citing Literature Volume69, Issue414 April 1997Pages 433-434 ReferencesRelatedInformation