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14. Domain-specific mutations in TGFB1 result in Camurati-Engelmann disease. Kinoshita A; Saito T; Tomita H; Makita Y; Yoshida K; Ghadami M; Yamada K; Kondo S; Ikegawa S; Nishimura G; Fukushima Y; Nakagomi T; Saito H; Sugimoto T; Kamegaya M; Hisa K; Murray JC; Taniguchi N; Niikawa N; Yoshiura K Nat Genet; 2000 Sep; 26(1):19-20. PubMed ID: 10973241 [TBL] [Abstract][Full Text] [Related]
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16. [Transitory myelofibrosis in a case of diaphyseal dysplasia (Camurati-Engelmann's disease) (author's transl)]. Emons D; Hussel D; Bechrakis G; Födisch HJ Rofo; 1978 Jan; 128(1):70-4. PubMed ID: 146665 [TBL] [Abstract][Full Text] [Related]
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19. Camurati-Engelmann disease type II: progressive diaphyseal dysplasia with striations of the bones. Nishimura G; Nishimura H; Tanaka Y; Makita Y; Ikegawa S; Ghadami M; Kinoshita A; Niikawa N Am J Med Genet; 2002 Jan; 107(1):5-11. PubMed ID: 11807860 [TBL] [Abstract][Full Text] [Related]
20. Localisation of the gene causing diaphyseal dysplasia Camurati-Engelmann to chromosome 19q13. Janssens K; Gershoni-Baruch R; Van Hul E; Brik R; Guañabens N; Migone N; Verbruggen LA; Ralston SH; Bonduelle M; Van Maldergem L; Vanhoenacker F; Van Hul W J Med Genet; 2000 Apr; 37(4):245-9. PubMed ID: 10745041 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]