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Japanese founder duplications/triplications involving BHLHA9 are associated with split-hand/foot malformation with or without long bone deficiency and Gollop-Wolfgang complex.
Nagata E, Kano H, Kato F, Yamaguchi R, Nakashima S, Takayama S, Kosaki R, Tonoki H, Mizuno S, Watanabe S, Yoshiura K, Kosho T, Hasegawa T, Kimizuka M, Suzuki A, Shimizu K, Ohashi H, Haga N, Numabe H, Horii E, Nagai T, Yoshihashi H, Nishimura G, Toda T, Takada S, Yokoyama S, Asahara H, Sano S, Fukami M, Ikegawa S, Ogata T. Nagata E, et al. Among authors: haga n. Orphanet J Rare Dis. 2014 Oct 21;9:125. doi: 10.1186/s13023-014-0125-5. Orphanet J Rare Dis. 2014. PMID: 25351291 Free PMC article.
Syringohydromyelia in Hajdu-Cheney syndrome.
Nishimura G, Aoki K, Haga N, Hasegawa T. Nishimura G, et al. Among authors: haga n. Pediatr Radiol. 1996;26(1):59-61. doi: 10.1007/BF01403708. Pediatr Radiol. 1996. PMID: 8598999
Spondylar dysplasia in type X collagenopathy.
Nishimura G, Manabe N, Kosaki K, Haga N, Ohashi H, Nakamura K, Ikegawa S. Nishimura G, et al. Among authors: haga n. Pediatr Radiol. 2001 Feb;31(2):76-80. doi: 10.1007/s002470000394. Pediatr Radiol. 2001. PMID: 11214689
Association analysis of single nucleotide polymorphisms in cartilage-specific collagen genes with knee and hip osteoarthritis in the Japanese population.
Ikeda T, Mabuchi A, Fukuda A, Kawakami A, Ryo Y, Yamamoto S, Miyoshi K, Haga N, Hiraoka H, Takatori Y, Kawaguchi H, Nakamura K, Ikegawa S. Ikeda T, et al. Among authors: haga n. J Bone Miner Res. 2002 Jul;17(7):1290-6. doi: 10.1359/jbmr.2002.17.7.1290. J Bone Miner Res. 2002. PMID: 12096843 Free article.
462 results