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2. An integrated approach to management of Marfan syndrome caused by an FBN1 exon 18 mutation in an Australian Aboriginal family. Summers KM; Xu D; West JA; McGill JJ; Galbraith A; Whight CM; Brocque SL; Nataatmadja M; Kong LK; Dondey J; Stark D; West MJ Clin Genet; 2004 Jan; 65(1):66-9. PubMed ID: 15032979 [No Abstract] [Full Text] [Related]
3. Rheumatoid arthritis and Australian aboriginals. Roberts-Thomson PJ; Hedger S; Bossingham D Med J Aust; 1998 Jan; 168(2):92. PubMed ID: 9469191 [No Abstract] [Full Text] [Related]
4. Use of the arm-span to height ratio as a criterion for Marfan syndrome in Aboriginal Australians: Diagnostically challenging. McInerney-Leo AM; West JA; McGill JJ; Brown MA; Duncan EL; West MJ Am J Med Genet A; 2020 Apr; 182(4):829-830. PubMed ID: 31943716 [No Abstract] [Full Text] [Related]
5. First report of the genetic background of Marfan syndrome in Polish patients. Wypasek E; Potaczek DP; Stąpor R; Coucke PJ; De Backer J; De Paepe AM; Undas A Pol Arch Med Wewn; 2013; 123(11):646-7. PubMed ID: 24296667 [No Abstract] [Full Text] [Related]
7. Segregation of all four major fibrillar collagen genes in the Marfan syndrome. Ogilvie DJ; Wordsworth BP; Priestley LM; Dalgleish R; Schmidtke J; Zoll B; Sykes BC Am J Hum Genet; 1987 Dec; 41(6):1071-82. PubMed ID: 3479900 [TBL] [Abstract][Full Text] [Related]
8. A suggestion of linkage between the Marfan syndrome and the rhesus blood group. Mace M Clin Genet; 1979 Aug; 16(2):96-102. PubMed ID: 113151 [TBL] [Abstract][Full Text] [Related]
9. Co-occurrence of Marfan syndrome and schizophrenia: what can be learned? Van Den Bossche MJ; Van Wallendael KL; Strazisar M; Sabbe B; Del-Favero J Eur J Med Genet; 2012 Apr; 55(4):252-5. PubMed ID: 22406088 [TBL] [Abstract][Full Text] [Related]
10. Clinical variability in the Marfan syndrome(s). Pyeritz RE; Murphy EA; McKusick VA Birth Defects Orig Artic Ser; 1979; 15(5B):155-78. PubMed ID: 526577 [No Abstract] [Full Text] [Related]
11. Marfan syndrome affecting four generations of a family without ocular involvement. Bridges AB; Faed M; Boxer M; Haining WM; Pringle TH; McNeill GP Postgrad Med J; 1991 Jun; 67(788):538-42. PubMed ID: 1924022 [TBL] [Abstract][Full Text] [Related]
12. Congenital contractural arachnodactyly, keratoconus, and probable Marfan syndrome in the same pedigree. Bass HN; Sparkes RS; Crandall BF; Marcy SM J Pediatr; 1981 Apr; 98(4):591-3. PubMed ID: 7205489 [No Abstract] [Full Text] [Related]
13. [A pedigree with Marfan syndrome]. Geng Y Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2015 Apr; 32(2):299. PubMed ID: 25863106 [No Abstract] [Full Text] [Related]
15. [Current genetic information on Marfan's syndrome]. Fazekas A; Vigváry L Orv Hetil; 1971 May; 112(22):1277-80. PubMed ID: 5566466 [No Abstract] [Full Text] [Related]
16. [Marfan syndrome--a case report]. Weh M; Gudowski G; Adrian B Kinderarztl Prax; 1985 Apr; 53(4):185-91. PubMed ID: 4010158 [No Abstract] [Full Text] [Related]
17. Novel FBN1 mutation in a family with inherited Marfan Syndrome: p.Cys2672Arg. Cetinkaya A; Karaman A; Mutlu MB; Yavuz T Congenit Anom (Kyoto); 2018 Jan; 58(1):41-43. PubMed ID: 28321935 [No Abstract] [Full Text] [Related]
18. Coronavirus-like particles in Aboriginals and non-Aboriginals in Western Australia. Schnagl RD; Holmes IH; Mackay-Scollay EM Med J Aust; 1978 Mar; 1(6):307-9. PubMed ID: 661689 [TBL] [Abstract][Full Text] [Related]
19. Exclusion of the alpha 2(I) and alpha 1(III) collagen genes as the mutant loci in a Marfan syndrome family. Dalgleish R; Hawkins JR; Keston M J Med Genet; 1987 Mar; 24(3):148-51. PubMed ID: 2883320 [TBL] [Abstract][Full Text] [Related]