Results: 1-3 |
Results: 3
SHH mutation is associated with solitary median maxillary central incisor:A study of 13 patients and review of the literature
Authors: Nanni, L Ming, JE Du, YZ Hall, RK Aldred, M Bankier, A Muenke, M
Citation: L. Nanni et al., SHH mutation is associated with solitary median maxillary central incisor:A study of 13 patients and review of the literature, AM J MED G, 102(1), 2001, pp. 1-10
Germline mutations in BMPR1A/ALK3 cause a subset of cases of juvenile polyposis syndrome and of Cowden and Bannayan-Riley-Ruvalcaba syndromes
Authors: Zhou, XP Woodford-Richens, K Lehtonen, R Kurose, K Aldred, M Hampel, H Launonen, V Virta, S Pilarski, R Salovaara, R Bodmer, WF Conrad, BA Dunlop, M Hodgson, SV Iwama, T Jarvinen, H Kellokumpu, I Kim, JC Leggett, B Markie, D Mecklin, JP Neale, K Phillips, R Piris, J Rozen, P Houlston, RS Aaltonen, LA Tomlinson, IPM Eng, C
Citation: Xp. Zhou et al., Germline mutations in BMPR1A/ALK3 cause a subset of cases of juvenile polyposis syndrome and of Cowden and Bannayan-Riley-Ruvalcaba syndromes, AM J HU GEN, 69(4), 2001, pp. 704-711
A physical and transcript map based upon refinement of the critical interval for PPH1, a gene for familial primary pulmonary hypertension
Authors: Machado, RD Pauciulo, MW Fretwell, N Veal, C Thomson, JR Guell, CV Aldred, M Brannon, CA Trembath, RC Nichols, WC
Citation: Rd. Machado et al., A physical and transcript map based upon refinement of the critical interval for PPH1, a gene for familial primary pulmonary hypertension, GENOMICS, 68(2), 2000, pp. 220-228
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