Comment on

• Duplications and de novo deletions of the SMNt gene demonstrated by fluorescence-based carrier testing for spinal muscular atrophy.

  Chen KL, Wang YL, Rennert H, Joshi I, Mills JK, Leonard DG, Wilson RB. Chen KL, et al. Am J Med Genet. 1999 Aug 27;85(5):463-9. Am J Med Genet. 1999. PMID: 10405443
• SMN2-deletion in childhood-onset spinal muscular atrophy.

  Srivastava S, Mukherjee M, Panigrahi I, Shanker Pandey G, Pradhan S, Mittal B. Srivastava S, et al. Am J Med Genet. 2001 Jul 1;101(3):198-202. doi: 10.1002/ajmg.1386. Am J Med Genet. 2001. PMID: 11424133