Allele-specific amplification for preimplantation genetic diagnosis (PGD) of spinal muscular atrophy

Author:

Moutou Céline,Gardes Nathalie,Rongières Catherine,Ohl Jeanine,Bettahar-Lebugle Karima,Wittemer Christiane,Gerlinger Pierre,Viville Stéphane

Funder

Association Française contre les Myopathies (AFM)

Association Française de Lutte contre la Mucoviscidose (AFLM-VLM)

Publisher

Wiley

Subject

Genetics(clinical),Obstetrics and Gynaecology

Reference27 articles.

1. Spinal muscular atrophy: untangling the knot?;Biros;J Med Genet,1999

2. Assessment of multiplex fluorescent PCR for screening single cells for trisomy 21 and single gene defects;Blake;Mol Hum Reprod,1999

3. Genetic mapping of chronic childhood-onset spinal muscular atrophy to chromosome 5q11.2-13.3;Brzustowicz;Nature,1990

4. Structure and organization of the human survival motor neurone (SMN) gene;Burglen;Genomics,1996

5. Deletions of the survival motor neuron gene in unaffected siblings of patients with spinal muscular atrophy;Cobben;Am J Hum Genet,1995

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