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Agnathia‐Holoprosencephaly: A midline malformation association

1990; Wiley; Volume: 36; Issue: 4 Linguagem: Inglês

10.1002/ajmg.1320360436

1096-8628

Raoul C. M. Hennekam,

Cleft Lip and Palate Research

American Journal of Medical GeneticsVolume 36, Issue 4 p. 525-525 Letter to the Editor Agnathia-Holoprosencephaly: A midline malformation association Raoul C. M. Hennekam M.D., Corresponding Author Raoul C. M. Hennekam M.D. Clinical Genetics Center Utrecht Utrecht The NetherlandsClinical Genetics Center Utrecht, P.O. Box 18009, 3501 CA Utrecht, The NetherlandsSearch for more papers by this author Raoul C. M. Hennekam M.D., Corresponding Author Raoul C. M. Hennekam M.D. Clinical Genetics Center Utrecht Utrecht The NetherlandsClinical Genetics Center Utrecht, P.O. Box 18009, 3501 CA Utrecht, The NetherlandsSearch for more papers by this author First published: August 1990 https://doi.org/10.1002/ajmg.1320360436Citations: 11AboutPDF 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 Cohen MM, Jr (1989): Perspectives on holoprosencephaly: Part III. Spectra, distinctions, continuities and discontinuities. Am J Med Genet 34: 271–288. Hersh JH, McChane RH, Rosenberg EM, Powers WH, Jr, Corrigan C, Pancratz L (1989): Brief clinical report: Otocephaly—midline malformation association. Am J Med Genet 34: 246–249. Krassikoff N, Sekhon GS (1989): Letter to the editor: Familial agnathia-holoprosencephaly caused by an inherited unbalanced translocation and not autosomal recessive inheritance. Am J Med Genet 34: 255–257. Pauli RM, Graham JM, Jr, Barr M (1981): Agnathia, situs inversus, and associated malformations. Teratology 23: 85–93. Robinson HB, Lenke R (1989): Letter to the editor: Agnathia, holoprosencephaly, and situs inversus. Am J Med Genet 34: 266–267. Sperber GH, Honoré LH, Johnson ES (1986): Acalvaria, holoprosencephaly, and facial dysmorphism syndrome. J Craniofac Genet Dev Biol [Suppl] 2: 319–329. Vrolik W (1849): “ De Vrucht van den Mensch en van de Zoogdieren.” Amsterdam: GMP London CK Citing Literature Volume36, Issue4August 1990Pages 525-525 ReferencesRelatedInformation