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6. Prenatal prediction in families with autosomal recessive proximal spinal muscular atrophy (5q11.2-q13.3): molecular genetics and clinical experience in 109 cases. Wirth B; Rudnik-Schöneborn S; Hahnen E; Röhrig D; Zerres K Prenat Diagn; 1995 May; 15(5):407-17. PubMed ID: 7644431 [TBL] [Abstract][Full Text] [Related]
7. 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]
8. Linkage and apparent heterogeneity in proximal spinal muscular atrophies. Cobben JM; Scheffer H; De Visser M; Osinga J; Frants R; van der Steege G; Wijmenga C; ten Kate LP; van Ommen GJ; Buys CH Neuromuscul Disord; 1993 Jul; 3(4):327-33. PubMed ID: 8268730 [TBL] [Abstract][Full Text] [Related]
9. 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]
10. 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]
11. Isolation of microsatellites from the spinal muscular atrophy (SMA) candidate region on chromosome 5q and linkage analysis in Spanish SMA families. Velasco E; Valero C; García E; de la Puente A; Cruces J; San Millán JL; del Castillo I; Coloma A; Moreno F; Hernández-Chico C Eur J Hum Genet; 1995; 3(2):96-101. PubMed ID: 7552147 [TBL] [Abstract][Full Text] [Related]
12. Linkage analysis of spinal muscular atrophy. Daniels RJ; Thomas NH; MacKinnon RN; Lehner T; Ott J; Flint TJ; Dubowitz V; Ignatius J; Donner M; Zerres K Genomics; 1992 Feb; 12(2):335-9. PubMed ID: 1346777 [TBL] [Abstract][Full Text] [Related]
14. Distal infantile spinal muscular atrophy associated with paralysis of the diaphragm: a variant of infantile spinal muscular atrophy. Bertini E; Gadisseux JL; Palmieri G; Ricci E; Di Capua M; Ferriere G; Lyon G Am J Med Genet; 1989 Jul; 33(3):328-35. PubMed ID: 2801766 [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. Molecular analysis of candidate genes on chromosome 5q13 in autosomal recessive spinal muscular atrophy: evidence of homozygous deletions of the SMN gene in unaffected individuals. Hahnen E; Forkert R; Marke C; Rudnik-Schöneborn S; Schönling J; Zerres K; Wirth B Hum Mol Genet; 1995 Oct; 4(10):1927-33. PubMed ID: 8595417 [TBL] [Abstract][Full Text] [Related]
17. Molecular diagnosis of spinal muscular atrophy in Egyptians. Shawky RM; Abd el-Aleem K; Rifaat MM; Moustafa A East Mediterr Health J; 2001; 7(1-2):229-37. PubMed ID: 12596974 [TBL] [Abstract][Full Text] [Related]
18. Association between Ag1-CA alleles and severity of autosomal recessive proximal spinal muscular atrophy. DiDonato CJ; Morgan K; Carpten JD; Fuerst P; Ingraham SE; Prescott G; McPherson JD; Wirth B; Zerres K; Hurko O Am J Hum Genet; 1994 Dec; 55(6):1218-29. PubMed ID: 7977383 [TBL] [Abstract][Full Text] [Related]
20. 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] [Next] [New Search]