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134 related items for PubMed ID: 20447141
1. Stüve-Wiedemann syndrome: long-term follow-up and genetic heterogeneity. Jung C, Dagoneau N, Baujat G, Le Merrer M, David A, Di Rocco M, Hamel B, Mégarbané A, Superti-Furga A, Unger S, Munnich A, Cormier-Daire V. Clin Genet; 2010 Mar; 77(3):266-72. PubMed ID: 20447141 [Abstract] [Full Text] [Related]
3. Abnormal oral-pharyngeal swallowing as cause of morbidity and early death in Stüve-Wiedemann syndrome. Corona-Rivera JR, Cormier-Daire V, Dagoneau N, Coello-Ramírez P, López-Marure E, Romo-Huerta CO, Silva-Baez H, Aguirre-Salas LM, Estrada-Solorio MI. Eur J Med Genet; 2009 Mar; 52(4):242-6. PubMed ID: 19371797 [Abstract] [Full Text] [Related]
4. Long-term follow-up in Stuve-Wiedemann syndrome: a clinical report. Gaspar IM, Saldanha T, Cabral P, Vilhena MM, Tuna M, Costa C, Dagoneau N, Daire VC, Hennekam RC. Am J Med Genet A; 2008 Jul 01; 146A(13):1748-53. PubMed ID: 18546280 [Abstract] [Full Text] [Related]
17. Stuve-Wiedemann syndrome: a skeletal dysplasia characterized by bowed long bones. Begam MA, Alsafi W, Bekdache GN, Chedid F, Al-Gazali L, Mirghani HM. Ultrasound Obstet Gynecol; 2011 Nov 12; 38(5):553-8. PubMed ID: 21337444 [Abstract] [Full Text] [Related]
18. Stüve-Wiedemann syndrome and related bent bone dysplasias. Akawi NA, Ali BR, Al-Gazali L. Clin Genet; 2012 Jul 12; 82(1):12-21. PubMed ID: 22300393 [Abstract] [Full Text] [Related]