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7. Genetic linkage analysis of Canadian spinal muscular atrophy kindreds using flanking microsatellite 5q13 polymorphisms. MacKenzie A; Roy N; Besner A; Mettler G; Jacob P; Korneluk R; Surh L Hum Genet; 1993 Jan; 90(5):501-4. PubMed ID: 8094064 [TBL] [Abstract][Full Text] [Related]
8. Genetic homogeneity between acute and chronic forms of spinal muscular atrophy. Gilliam TC; Brzustowicz LM; Castilla LH; Lehner T; Penchaszadeh GK; Daniels RJ; Byth BC; Knowles J; Hislop JE; Shapira Y Nature; 1990 Jun; 345(6278):823-5. PubMed ID: 1972783 [TBL] [Abstract][Full Text] [Related]
9. Prenatal prediction of spinal muscular atrophy. Daniels RJ; Suthers GK; Morrison KE; Thomas NH; Francis MJ; Mathew CG; Loughlin S; Heiberg A; Wood D; Dubowitz V J Med Genet; 1992 Mar; 29(3):165-70. PubMed ID: 1348091 [TBL] [Abstract][Full Text] [Related]
10. Axonal neuropathy and predominance of type II myofibers in infantile spinal muscular atrophy. Omran H; Ketelsen UP; Heinen F; Sauer M; Rudnik-Schöneborn S; Wirth B; Zerres K; Kratzer W; Korinthenberg R J Child Neurol; 1998 Jul; 13(7):327-31. PubMed ID: 9701481 [TBL] [Abstract][Full Text] [Related]
11. Infantile spinal muscular atrophy variant with congenital fractures in a female neonate: evidence for autosomal recessive inheritance. Courtens W; Johansson AB; Dachy B; Avni F; Telerman-Toppet N; Scheffer H J Med Genet; 2002 Jan; 39(1):74-7. PubMed ID: 11826032 [No Abstract] [Full Text] [Related]
12. [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]
13. 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]
20. Proximal and distal spinal muscular atrophy in one family: molecular genetic studies provide further evidence for the non-allelic origin of both diseases. Spranger S; Rudnik-Schöneborn S; Spranger M; Schächtele M; Zerres K; Wirth B J Med Genet; 1997 Apr; 34(4):340-2. PubMed ID: 9138162 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]