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11. Mapping of acute (type I) spinal muscular atrophy to chromosome 5q12-q14. The French Spinal Muscular Atrophy Investigators. Melki J; Sheth P; Abdelhak S; Burlet P; Bachelot MF; Lathrop MG; Frezal J; Munnich A Lancet; 1990 Aug; 336(8710):271-3. PubMed ID: 1973971 [TBL] [Abstract][Full Text] [Related]
12. An investigation of genetic heterogeneity and linkage disequilibrium in 161 families with spinal muscular atrophy. Mérette C; Brzustowicz LM; Daniels RJ; Davies KE; Gilliam TC; Melki J; Munnich A; Pericak-Vance MA; Siddique T; Voosen B Genomics; 1994 May; 21(1):27-33. PubMed ID: 8088801 [TBL] [Abstract][Full Text] [Related]
13. Fine mapping and narrowing of the genetic interval of the spinal muscular atrophy region by linkage studies. Wirth B; Voosen B; Röhrig D; Knapp M; Piechaczek B; Rudnik-Schöneborn S; Zerres K Genomics; 1993 Jan; 15(1):113-8. PubMed ID: 8432521 [TBL] [Abstract][Full Text] [Related]
14. The use of chromosome 5q markers for confirming the diagnosis of proximal spinal muscular atrophy. Whittle MR; Zatz M; Reinach FC Braz J Med Biol Res; 1993 Nov; 26(11):1157-73. PubMed ID: 7907903 [TBL] [Abstract][Full Text] [Related]
15. Linkage analysis in spinal muscular atrophy, by six closely flanking markers on chromosome 5. Sheth P; Abdelhak S; Bachelot MF; Burlet P; Masset M; Hillaire D; Clerget-Darpoux F; Frézal J; Lathrop GM; Munnich A Am J Hum Genet; 1991 Apr; 48(4):764-8. PubMed ID: 2014799 [TBL] [Abstract][Full Text] [Related]
16. Fine-mapping of the spinal muscular atrophy locus to a region flanked by MAP1B and D5S6. Brzustowicz LM; Kleyn PW; Boyce FM; Lien LL; Monaco AP; Penchaszadeh GK; Das K; Wang CH; Munsat TL; Ott J Genomics; 1992 Aug; 13(4):991-8. PubMed ID: 1505990 [TBL] [Abstract][Full Text] [Related]
17. De novo and inherited deletions of the 5q13 region in spinal muscular atrophies. Melki J; Lefebvre S; Burglen L; Burlet P; Clermont O; Millasseau P; Reboullet S; Bénichou B; Zeviani M; Le Paslier D Science; 1994 Jun; 264(5164):1474-7. PubMed ID: 7910982 [TBL] [Abstract][Full Text] [Related]
18. No evidence for linkage of autosomal dominant proximal spinal muscular atrophies to chromosome 5q markers. Kausch K; Müller CR; Grimm T; Ricker K; Rietschel M; Rudnik-Schöneborn S; Zerres K Hum Genet; 1991 Jan; 86(3):317-8. PubMed ID: 1997389 [TBL] [Abstract][Full Text] [Related]
19. Assessment of nonallelic genetic heterogeneity of chronic (type II and III) spinal muscular atrophy. Brzustowicz LM; Mérette C; Kleyn PW; Lehner T; Castilla LH; Penchaszadeh GK; Das K; Munsat TL; Ott J; Gilliam TC Hum Hered; 1993; 43(6):380-7. PubMed ID: 7904586 [TBL] [Abstract][Full Text] [Related]
20. Refinement of the spinal muscular atrophy locus by genetic and physical mapping. Wang CH; Kleyn PW; Vitale E; Ross BM; Lien L; Xu J; Carter TA; Brzustowicz LM; Obici S; Selig S Am J Hum Genet; 1995 Jan; 56(1):202-9. PubMed ID: 7825579 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]