These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
140 related articles for article (PubMed ID: 9354841)
21. OSTEOGENESIS IMPERFECTA WITH ARTHROGRYPOSIS MULTIPLEX CONGENITA. SHARMA NL; ANAND JS J Indian Med Assoc; 1964 Aug; 43():124-6. PubMed ID: 14197943 [No Abstract] [Full Text] [Related]
22. Phenotypic and molecular characterization of Bruck syndrome (osteogenesis imperfecta with contractures of the large joints) caused by a recessive mutation in PLOD2. Ha-Vinh R; Alanay Y; Bank RA; Campos-Xavier AB; Zankl A; Superti-Furga A; Bonafé L Am J Med Genet A; 2004 Dec; 131(2):115-20. PubMed ID: 15523624 [TBL] [Abstract][Full Text] [Related]
23. A Rare Case of Bruck Syndrome Type 2 in Siblings With Broad Phenotypic Variability. Luce L; Casale M; Waldron S Ochsner J; 2020; 20(2):204-208. PubMed ID: 32612477 [No Abstract] [Full Text] [Related]
24. Arthrogryposis multiplex congenita in an Arab kindred: update. Jaber L; Weitz R; Bu X; Fischel-Ghodsian N; Rotter JI; Shohat M Am J Med Genet; 1995 Jan; 55(3):331-4. PubMed ID: 7726232 [TBL] [Abstract][Full Text] [Related]
25. Expanding the Clinical Spectrum of Phenotypes Caused by Pathogenic Variants in PLOD2. Leal GF; Nishimura G; Voss U; Bertola DR; Åström E; Svensson J; Yamamoto GL; Hammarsjö A; Horemuzova E; Papadiogannakis N; Iwarsson E; Grigelioniene G; Tham E J Bone Miner Res; 2018 Apr; 33(4):753-760. PubMed ID: 29178448 [TBL] [Abstract][Full Text] [Related]
26. Bruck syndrome - a rare syndrome of bone fragility and joint contracture and novel homozygous FKBP10 mutation. Moravej H; Karamifar H; Karamizadeh Z; Amirhakimi G; Atashi S; Nasirabadi S Endokrynol Pol; 2015; 66(2):170-4. PubMed ID: 25931047 [TBL] [Abstract][Full Text] [Related]
28. [Problems with reference to genetic counseling in arthrogryposis multiplex congenits]. Gericke GS; Retief AE; Van Niekerk WA S Afr Med J; 1975 Mar; 49(14):573-6. PubMed ID: 1145379 [TBL] [Abstract][Full Text] [Related]
29. Lethal autosomal recessive arthrogryposis multiplex congenita with whistling face and calcifications of the nervous system. Illum N; Reske-Nielsen E; Skovby F; Askjaer SA; Bernsen A Neuropediatrics; 1988 Nov; 19(4):186-92. PubMed ID: 3205375 [TBL] [Abstract][Full Text] [Related]
30. New insights on the clinical variability of FKBP10 mutations. Essawi OH; Tapaneeyaphan P; Symoens S; Gistelinck C C; Malfait F; Eyre DR; Essawi T; Callewaert B; Coucke PJ Eur J Med Genet; 2020 Sep; 63(9):103980. PubMed ID: 32531462 [TBL] [Abstract][Full Text] [Related]
33. Presentation of Rare Phenotypes Associated with the Merkuryeva ES; Markova TV; Kenis VM; Agranovich OE; Dan IM; Kotalevskaya YY; Shchagina OA; Ryzhkova OP; Fomenko SS; Dadali EL; Kutsev SI Genes (Basel); 2024 May; 15(6):. PubMed ID: 38927610 [TBL] [Abstract][Full Text] [Related]
34. A dominantly inherited form of arthrogryposis multiplex congenita with unusual dermatoglyphics. Sack GH Clin Genet; 1978 Dec; 14(6):317-23. PubMed ID: 729196 [TBL] [Abstract][Full Text] [Related]
35. Mutation In Fkbp10 Gene Cause Bruck Syndrome 1 (Brks1) In A Pakistani Family Of Pashtun Origin. Tauseef U; Ibrahim M; Noor N; Hanif M J Ayub Med Coll Abbottabad; 2023; 35(2):341-347. PubMed ID: 37422836 [TBL] [Abstract][Full Text] [Related]
36. Novel mutations in FKBP10 and PLOD2 cause rare Bruck syndrome in Chinese patients. Zhou P; Liu Y; Lv F; Nie M; Jiang Y; Wang O; Xia W; Xing X; Li M PLoS One; 2014; 9(9):e107594. PubMed ID: 25238597 [TBL] [Abstract][Full Text] [Related]
37. The first case of Bruck syndrome associated with gastroschisis. Afşarlar ÇE; Peltek-Kendirci HN; Erdoğan D; Özgüner İF; Çavuşoğlu YH; Karaman A; Çetinkaya S Turk J Pediatr; 2013; 55(6):651-4. PubMed ID: 24577988 [TBL] [Abstract][Full Text] [Related]
38. The ocular form of osteogenesis imperfecta: a new autosomal recessive syndrome. Beighton P; Winship I; Behari D Clin Genet; 1985 Jul; 28(1):69-75. PubMed ID: 4028503 [TBL] [Abstract][Full Text] [Related]
39. Non-lethal arthrogryposis multiplex congenita presenting with cystic hygroma at 13 weeks gestational age. Scott H; Hunter A; Bédard B Prenat Diagn; 1999 Oct; 19(10):966-71. PubMed ID: 10521824 [TBL] [Abstract][Full Text] [Related]
40. Arthrogryposis multiplex congenita: twenty-three cases in an Arab kindred. Lebenthal E; Shochet SB; Adam A; Seelenfreund M; Fried A; Najenson T; Sandbank U; Matoth Y Pediatrics; 1970 Dec; 46(6):891-9. PubMed ID: 5491443 [No Abstract] [Full Text] [Related] [Previous] [Next] [New Search]