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25. From enigmatic to problematic: the new molecular genetics of childhood spinal muscular atrophy. Crawford TO Neurology; 1996 Feb; 46(2):335-40. PubMed ID: 8614490 [No Abstract] [Full Text] [Related]
27. Transmission ratio distortion in the spinal muscular atrophy locus: data from 314 prenatal tests. Botta A; Tacconelli A; Bagni I; Giardina E; Bonifazi E; Pietropolli A; Clementi M; Novelli G Neurology; 2005 Nov; 65(10):1631-5. PubMed ID: 16301493 [TBL] [Abstract][Full Text] [Related]
28. 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]
29. Spinal muscular atrophy of childhood: genetics. Raymond FL Dev Med Child Neurol; 1997 Jun; 39(6):419-20. PubMed ID: 9233369 [No Abstract] [Full Text] [Related]
30. Controversy over Werdnig-Hoffmann disease and multiple system atrophy. Chou SM Curr Opin Neurol; 1993 Dec; 6(6):861-4. PubMed ID: 8293160 [No Abstract] [Full Text] [Related]
31. Two novel microsatellite markers for prenatal prediction of spinal muscular atrophy (SMA). Morrison KE; Daniels RJ; Suthers GK; Flynn GA; Francis MJ; Grewal PK; Dennis C; Buckle V; Ignatius J; Dubowitz V Hum Genet; 1993 Sep; 92(2):133-8. PubMed ID: 8370578 [TBL] [Abstract][Full Text] [Related]
32. A recombination event occurring within two complex 5q13.1 microsatellite repeat polymorphisms suggests a telomeric mapping of spinal muscular atrophy. Yaraghi Z; McLean MD; Roy N; Surh L; Ikeda JE; Korneluk RG; MacKenzie A Hum Genet; 1995 Sep; 96(3):330-4. PubMed ID: 7649551 [TBL] [Abstract][Full Text] [Related]
34. Exclusion of the gene locus for spinal muscular atrophy on chromosome 5q in a family with infantile olivopontocerebellar atrophy (OPCA) and anterior horn cell degeneration. Rudnik-Schöneborn S; Wirth B; Röhrig D; Saule H; Zerres K Neuromuscul Disord; 1995 Jan; 5(1):19-23. PubMed ID: 7719136 [TBL] [Abstract][Full Text] [Related]
37. [Genetic diagnosis of the hypotonic newborn]. Bauer MS Rev Neurol; 1997 May; 25(141):703-6. PubMed ID: 9206594 [TBL] [Abstract][Full Text] [Related]
38. High-resolution genetic map around the spinal muscular atrophy (SMA) locus on chromosome 5. Morrison KE; Daniels RJ; Suthers GK; Flynn GA; Francis MJ; Buckle VJ; Davies KE Am J Hum Genet; 1992 Mar; 50(3):520-7. PubMed ID: 1539593 [TBL] [Abstract][Full Text] [Related]
39. Pictorial essay of Werdnig-Hoffman disease. Poggiani C; Ferrari D; Parati S; Torresani P Minerva Pediatr; 2009 Apr; 61(2):237-8. PubMed ID: 19322128 [No Abstract] [Full Text] [Related]
40. [The spectrum of spinal muscular atrophies: a population study]. Rudenskaia GE; Mamedova RA Zh Nevrol Psikhiatr Im S S Korsakova; 1997; 97(8):22-5. PubMed ID: 9343477 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]