150 related articles for article (PubMed ID: 9345093)
1. A gene for arthrogryposis multiplex congenita neuropathic type is linked to D5S394 on chromosome 5qter.
Shohat M; Lotan R; Magal N; Shohat T; Fischel-Ghodsian N; Rotter JI; Jaber L
Am J Hum Genet; 1997 Nov; 61(5):1139-43. PubMed ID: 9345093
[TBL] [Abstract][Full Text] [Related]
2. Fine mapping places the gene for arthrogryposis multiplex congenita neuropathic type between D5S394 and D5S2069 on chromosome 5qter.
Tanamy MG; Magal N; Halpern GJ; Jaber L; Shohat M
Am J Med Genet; 2001 Nov; 104(2):152-6. PubMed ID: 11746047
[TBL] [Abstract][Full Text] [Related]
3. Mutations in ERGIC1 cause Arthrogryposis multiplex congenita, neuropathic type.
Reinstein E; Drasinover V; Lotan R; Gal-Tanamy M; Bolocan Nachman I; Eyal E; Jaber L; Magal N; Shohat M
Clin Genet; 2018 Jan; 93(1):160-163. PubMed ID: 28317099
[TBL] [Abstract][Full Text] [Related]
4. Arthrogryposis multiplex congenita (AMC), a hereditary disease in swine, maps to chromosome 5 by linkage analysis.
Genini S; Malek M; Spilar S; Nguyen TT; Ménétrey F; Gebert S; Hagger C; Neuenschwander S; Kadarmideen HN; Stranzinger G; Vögeli P
Mamm Genome; 2004 Nov; 15(11):935-41. PubMed ID: 15672597
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Expanding the MYBPC1 phenotypic spectrum: a novel homozygous mutation causes arthrogryposis multiplex congenita.
Ekhilevitch N; Kurolap A; Oz-Levi D; Mory A; Hershkovitz T; Ast G; Mandel H; Baris HN
Clin Genet; 2016 Jul; 90(1):84-9. PubMed ID: 26661508
[TBL] [Abstract][Full Text] [Related]
7. Newly described form of X-linked arthrogryposis maps to the long arm of the human X chromosome.
Zori RT; Gardner JL; Zhang J; Mullan MJ; Shah R; Osborn AR; Houlden H; Wallace MR; Roberts S; Yang TP
Am J Med Genet; 1998 Aug; 78(5):450-4. PubMed ID: 9714012
[TBL] [Abstract][Full Text] [Related]
8. Autozygosity mapping, to chromosome 11q25, of a rare autosomal recessive syndrome causing histiocytosis, joint contractures, and sensorineural deafness.
Moynihan LM; Bundey SE; Heath D; Jones EL; McHale DP; Mueller RF; Markham AF; Lench NJ
Am J Hum Genet; 1998 May; 62(5):1123-8. PubMed ID: 9545394
[TBL] [Abstract][Full Text] [Related]
9. Genome-wide linkage scan, fine mapping, and haplotype analysis in a large, inbred, Arab Israeli pedigree suggest a schizophrenia susceptibility locus on chromosome 20p13.
Teltsh O; Kanyas K; Karni O; Levi A; Korner M; Ben-Asher E; Lancet D; Hamdan A; Lerer B; Kohn Y
Am J Med Genet B Neuropsychiatr Genet; 2008 Mar; 147B(2):209-15. PubMed ID: 17823922
[TBL] [Abstract][Full Text] [Related]
10. Linkage mapping of the locus for inherited ovine arthrogryposis (IOA) to sheep chromosome 5.
Murphy AM; MacHugh DE; Park SD; Scraggs E; Haley CS; Lynn DJ; Boland MP; Doherty ML
Mamm Genome; 2007 Jan; 18(1):43-52. PubMed ID: 17242863
[TBL] [Abstract][Full Text] [Related]
11. Genetics of arthrogryposis: linkage analysis approach.
Narkis G; Landau D; Manor E; Ofir R; Birk OS
Clin Orthop Relat Res; 2007 Mar; 456():30-5. PubMed ID: 17195815
[TBL] [Abstract][Full Text] [Related]
12. Mutation of SYNE-1, encoding an essential component of the nuclear lamina, is responsible for autosomal recessive arthrogryposis.
Attali R; Warwar N; Israel A; Gurt I; McNally E; Puckelwartz M; Glick B; Nevo Y; Ben-Neriah Z; Melki J
Hum Mol Genet; 2009 Sep; 18(18):3462-9. PubMed ID: 19542096
[TBL] [Abstract][Full Text] [Related]
13. A CHRNB1 frameshift mutation is associated with familial arthrogryposis multiplex congenita in Red dairy cattle.
Agerholm JS; McEvoy FJ; Menzi F; Jagannathan V; Drögemüller C
BMC Genomics; 2016 Jun; 17():479. PubMed ID: 27364156
[TBL] [Abstract][Full Text] [Related]
14. A gene for distal arthrogryposis type I maps to the pericentromeric region of chromosome 9.
Bamshad M; Watkins WS; Zenger RK; Bohnsack JF; Carey JC; Otterud B; Krakowiak PA; Robertson M; Jorde LB
Am J Hum Genet; 1994 Dec; 55(6):1153-8. PubMed ID: 7977374
[TBL] [Abstract][Full Text] [Related]
15. A gene for a severe lethal form of X-linked arthrogryposis (X-linked infantile spinal muscular atrophy) maps to human chromosome Xp11.3-q11.2.
Kobayashi H; Baumbach L; Matise TC; Schiavi A; Greenberg F; Hoffman EP
Hum Mol Genet; 1995 Jul; 4(7):1213-6. PubMed ID: 8528211
[TBL] [Abstract][Full Text] [Related]
16. Novel mutations in TPM2 and PIEZO2 are responsible for distal arthrogryposis (DA) 2B and mild DA in two Chinese families.
Li S; You Y; Gao J; Mao B; Cao Y; Zhao X; Zhang X
BMC Med Genet; 2018 Oct; 19(1):179. PubMed ID: 30285720
[TBL] [Abstract][Full Text] [Related]
17. Localization of the gene for thiamine-responsive megaloblastic anemia syndrome, on the long arm of chromosome 1, by homozygosity mapping.
Neufeld EJ; Mandel H; Raz T; Szargel R; Yandava CN; Stagg A; Fauré S; Barrett T; Buist N; Cohen N
Am J Hum Genet; 1997 Dec; 61(6):1335-41. PubMed ID: 9399900
[TBL] [Abstract][Full Text] [Related]
18. A gene for pyridoxine-dependent epilepsy maps to chromosome 5q31.
Cormier-Daire V; Dagoneau N; Nabbout R; Burglen L; Penet C; Soufflet C; Desguerre I; Munnich A; Dulac O
Am J Hum Genet; 2000 Oct; 67(4):991-3. PubMed ID: 10978228
[TBL] [Abstract][Full Text] [Related]
19. Homozygosity mapping places the acrodermatitis enteropathica gene on chromosomal region 8q24.3.
Wang K; Pugh EW; Griffen S; Doheny KF; Mostafa WZ; al-Aboosi MM; el-Shanti H; Gitschier J
Am J Hum Genet; 2001 Apr; 68(4):1055-60. PubMed ID: 11254458
[TBL] [Abstract][Full Text] [Related]
20. Linkage analysis of candidate regions in Swedish nonsyndromic cleft lip with or without cleft palate families.
Wong FK; Hagberg C; Karsten A; Larson O; Gustavsson M; Huggare J; Larsson C; Teh BT; Linder-Aronson S
Cleft Palate Craniofac J; 2000 Jul; 37(4):357-62. PubMed ID: 10912714
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
