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8. The protein kinase N (PKN) gene PRKCL1/Prkcl1 maps to human chromosome 19p12-p13.1 and mouse chromosome 8 with close linkage to the myodystrophy (myd) mutation. Bartsch JW; Mukai H; Takahashi N; Ronsiek M; Fuchs S; Jockusch H; Ono Y Genomics; 1998 Apr; 49(1):129-32. PubMed ID: 9570957 [TBL] [Abstract][Full Text] [Related]
9. Fish mapping of 250 cosmid and 26 YAC clones to chromosome 4 with special emphasis on the FSHD region at 4q35. Wijmenga C; Dauwerse HG; Padberg GW; Meyer N; Murray JC; Mills K; van Ommen GB; Hofker MH; Frants RR Muscle Nerve Suppl; 1995; 2():S14-8. PubMed ID: 7739620 [TBL] [Abstract][Full Text] [Related]
11. Towards the finer mapping of facioscapulohumeral muscular dystrophy at 4q35: construction of a laser microdissection library. Upadhyaya M; Osborn M; Maynard J; Altherr M; Ikeda J; Harper PS Am J Med Genet; 1995 Jun; 60(3):244-51. PubMed ID: 7573180 [TBL] [Abstract][Full Text] [Related]
12. The FSHD-linked locus D4F104S1 (p13E-11) on 4q35 has a homologue on 10qter. Bakker E; Wijmenga C; Vossen RH; Padberg GW; Hewitt J; van der Wielen M; Rasmussen K; Frants RR Muscle Nerve Suppl; 1995; 2():S39-44. PubMed ID: 7739624 [TBL] [Abstract][Full Text] [Related]
13. Genetic and physical mapping at the limb-girdle muscular dystrophy locus (LGMD2B) on chromosome 2p. Bashir R; Keers S; Strachan T; Passos-Bueno R; Zatz M; Weissenbach J; Le Paslier D; Meisler M; Bushby K Genomics; 1996 Apr; 33(1):46-52. PubMed ID: 8617508 [TBL] [Abstract][Full Text] [Related]
14. [Genetic analysis of facioscapulohumeral muscular dystrophy (FSHD)]. Goto K; Song MD; Lee JH; Arahata K Rinsho Shinkeigaku; 1995 Dec; 35(12):1416-8. PubMed ID: 8752415 [TBL] [Abstract][Full Text] [Related]
15. Characterization of a tandemly repeated 3.3-kb KpnI unit in the facioscapulohumeral muscular dystrophy (FSHD) gene region on chromosome 4q35. Lee JH; Goto K; Matsuda C; Arahata K Muscle Nerve Suppl; 1995; 2():S6-13. PubMed ID: 7739628 [TBL] [Abstract][Full Text] [Related]
16. Search for the FSHD gene using cDNA selection in a region spanning 100 kb on chromosome 4q35. van Deutekom JC; Hofker MH; Romberg S; van Geel M; Rommens J; Wright TJ; Hewitt JE; Padberg GW; Wijmenga C; Frants RR Muscle Nerve Suppl; 1995; 2():S19-26. PubMed ID: 7739621 [TBL] [Abstract][Full Text] [Related]
17. Localization of the region homologous to the Duchenne muscular dystrophy locus on the mouse X chromosome. Heilig R; Lemaire C; Mandel JL; Dandolo L; Amar L; Avner P Nature; 1987 Jul 9-15; 328(6126):168-70. PubMed ID: 3600794 [TBL] [Abstract][Full Text] [Related]
18. Cloning and mapping of a very short (10-kb) EcoRI fragment associated with facioscapulohumeral muscular dystrophy (FSHD). Lee JH; Goto K; Sahashi K; Nonaka I; Matsuda C; Arahata K Muscle Nerve Suppl; 1995; 2():S27-31. PubMed ID: 7739622 [TBL] [Abstract][Full Text] [Related]
19. [A family with facioscapulohumeral muscular dystrophy and hereditary long QT syndrome]. Kimura T; Moriwaki T; Sawada J; Naka T; Hazama T; Nakata T Rinsho Shinkeigaku; 1997 Aug; 37(8):690-2. PubMed ID: 9404145 [TBL] [Abstract][Full Text] [Related]
20. aku, a mutation of the mouse homologous to human alkaptonuria, maps to chromosome 16. Montagutelli X; Lalouette A; Coudé M; Kamoun P; Forest M; Guénet JL Genomics; 1994 Jan; 19(1):9-11. PubMed ID: 8188247 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]