These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
158 related articles for article (PubMed ID: 7633412)
1. Deletions in the survival motor neuron gene on 5q13 in autosomal recessive spinal muscular atrophy. Rodrigues NR; Owen N; Talbot K; Ignatius J; Dubowitz V; Davies KE Hum Mol Genet; 1995 Apr; 4(4):631-4. PubMed ID: 7633412 [TBL] [Abstract][Full Text] [Related]
2. 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]
3. Molecular analysis of the SMN and NAIP genes in Spanish spinal muscular atrophy (SMA) families and correlation between number of copies of cBCD541 and SMA phenotype. Velasco E; Valero C; Valero A; Moreno F; Hernández-Chico C Hum Mol Genet; 1996 Feb; 5(2):257-63. PubMed ID: 8824882 [TBL] [Abstract][Full Text] [Related]
4. An update of the mutation spectrum of the survival motor neuron gene (SMN1) in autosomal recessive spinal muscular atrophy (SMA). Wirth B Hum Mutat; 2000; 15(3):228-37. PubMed ID: 10679938 [TBL] [Abstract][Full Text] [Related]
5. Sequence of a 131-kb region of 5q13.1 containing the spinal muscular atrophy candidate genes SMN and NAIP. Chen Q; Baird SD; Mahadevan M; Besner-Johnston A; Farahani R; Xuan J; Kang X; Lefebvre C; Ikeda JE; Korneluk RG; MacKenzie AE Genomics; 1998 Feb; 48(1):121-7. PubMed ID: 9503025 [TBL] [Abstract][Full Text] [Related]
6. A frame-shift deletion in the survival motor neuron gene in Spanish spinal muscular atrophy patients. Bussaglia E; Clermont O; Tizzano E; Lefebvre S; Bürglen L; Cruaud C; Urtizberea JA; Colomer J; Munnich A; Baiget M Nat Genet; 1995 Nov; 11(3):335-7. PubMed ID: 7581461 [TBL] [Abstract][Full Text] [Related]
7. 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]
8. Allelic association and deletions in autosomal recessive proximal spinal muscular atrophy: association of marker genotype with disease severity and candidate cDNAs. Wirth B; Hahnen E; Morgan K; DiDonato CJ; Dadze A; Rudnik-Schöneborn S; Simard LR; Zerres K; Burghes AH Hum Mol Genet; 1995 Aug; 4(8):1273-84. PubMed ID: 7581364 [TBL] [Abstract][Full Text] [Related]
9. Gene conversion at the SMN locus in autosomal recessive spinal muscular atrophy does not predict a mild phenotype. Talbot K; Rodrigues NR; Ignatius J; Muntoni F; Davies KE Neuromuscul Disord; 1997 May; 7(3):198-201. PubMed ID: 9185185 [TBL] [Abstract][Full Text] [Related]
10. The mouse region syntenic for human spinal muscular atrophy lies within the Lgn1 critical interval and contains multiple copies of Naip exon 5. Scharf JM; Damron D; Frisella A; Bruno S; Beggs AH; Kunkel LM; Dietrich WF Genomics; 1996 Dec; 38(3):405-17. PubMed ID: 8975718 [TBL] [Abstract][Full Text] [Related]