Produção Nacional
Revisado por pares
Single median maxillary central incisor, hypophyseal tumor, andSHH mutation
2005; Wiley; Volume: 136A; Issue: 4 Linguagem: Inglês
10.1002/ajmg.a.30625
ISSN1552-4833
AutoresLucilene Arilho Ribeiro, Antônio Richieri‐Costa,
Tópico(s)Cleft Lip and Palate Research
ResumoAmerican Journal of Medical Genetics Part AVolume 136A, Issue 4 p. 346-347 Correspondence Single median maxillary central incisor, hypophyseal tumor, and SHH mutation Lucilene Arilho Ribeiro, Lucilene Arilho Ribeiro Serviço de Genética Clínica, Hospital de Reabilitação de Anomalias Craniofaciais, Universidade de São Paulo, Bauru, SP, BrazilSearch for more papers by this authorAntonio Richieri-Costa, Corresponding Author Antonio Richieri-Costa Serviço de Genética Clínica, Hospital de Reabilitação de Anomalias Craniofaciais, Universidade de São Paulo, Bauru, SP, BrazilServiço de Genética Clínica, Hospital de Reabilitação de Anomalias Craniofaciais, Universidade de São Paulo, Bauru, São Paulo, Brazil.Search for more papers by this author Lucilene Arilho Ribeiro, Lucilene Arilho Ribeiro Serviço de Genética Clínica, Hospital de Reabilitação de Anomalias Craniofaciais, Universidade de São Paulo, Bauru, SP, BrazilSearch for more papers by this authorAntonio Richieri-Costa, Corresponding Author Antonio Richieri-Costa Serviço de Genética Clínica, Hospital de Reabilitação de Anomalias Craniofaciais, Universidade de São Paulo, Bauru, SP, BrazilServiço de Genética Clínica, Hospital de Reabilitação de Anomalias Craniofaciais, Universidade de São Paulo, Bauru, São Paulo, Brazil.Search for more papers by this author First published: 07 June 2005 https://doi.org/10.1002/ajmg.a.30625Citations: 11Read the full textAboutPDF 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. 2003. The hedgehog signaling network. Am J Med Genet 123: 5–28. Garavelli L, Zanacca C, Caselli G, Banchini G, Dubourg C, David V, Odent S, Gurrieri F, Neri G. 2004. Solitary median maxillary central incisor syndrome: Clinical case with a novel mutation of sonic hedgehog. Am J Med Genet 127: 93–95. Hehr U, Gross C, Diebold U, Wahl D, Beudt U, Heidemann P, Hehr A, Mueller D. 2004. Wide phenotypic variability in families with holoprosencephaly and a sonic hedgehog mutation. Eur J Pediatr 163: 347–352. Lazaro L, Dubourg C, Pasquier L, Le Duff F, Blayau M, Durou MR, de la Pintiere AT, Aguilella C, David V, Odent S. 2004. Phenotypic and molecular variability of the holoprosencephalic spectrum. Am J Med Genet 129: 21–24. Marini M, Cusano R, De Biasio P, Caroli F, Lerone M, Silengo M, Ravazzolo R, Seri M, Camera G. 2003. Previously undescribed nonsense mutation in SHH caused autosomal dominant holoprosencephaly with wide intrafamilial variability. Am J Med Genet 117: 112–115. Nanni L, Ming JE, Du Y, Hall RK, Aldred M, Bankier A, Muenke M. 2001. SHH mutation is associated with solitary median maxillary central incisor: A study of 13 patients and review of the literature. Am J Med Genet 102: 1–10. Treier M, O'Connell S, Gleiberman A, Price J, Szeto DP, Burgess R, Chuang PT, McMahon AP, Rosenfeld MG. 2001. Hedgehog signaling is required for pituitary gland development. Development 128: 377–386. Citing Literature Volume136A, Issue41 August 2005Pages 346-347 ReferencesRelatedInformation
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