An 11 base pair duplication in exon 6 of the SMN gene produces a type I spinal muscular atrophy (SMA) phenotype: further evidence for SMN as the primary SMA …
DW Parsons, PE McAndrew, UR Monani… - Human molecular …, 1996 - academic.oup.com
The gene for autosomal recessive spinal muscular atrophy (SMA) has been mapped to 5q12
in a region that contains repeated markers and genes. Three cDNAs that detect deletions in …
in a region that contains repeated markers and genes. Three cDNAs that detect deletions in …
An 11 base pair duplication in exon 6 of the SMN gene produces a type I spinal muscular atrophy (SMA) phenotype: further evidence for SMN as the primary SMA …
DW Parsons, PE McAndrew… - Human molecular …, 1996 - pubmed.ncbi.nlm.nih.gov
The gene for autosomal recessive spinal muscular atrophy (SMA) has been mapped to 5q12
in a region that contains repeated markers and genes. Three cDNAs that detect deletions in …
in a region that contains repeated markers and genes. Three cDNAs that detect deletions in …
[PDF][PDF] An 11 base pair duplication in exon 6 of the SMN gene produces a type I spinal muscular atrophy (SMA) phenotype: further evidence for SMN as the primary …
DW Parsons, PE McAndrew, UR Monani… - Human Molecular …, 1996 - Citeseer
The gene for autosomal recessive spinal muscular atrophy (SMA) has been mapped to 5q12
in a region that contains repeated markers and genes. Three cDNAs that detect deletions in …
in a region that contains repeated markers and genes. Three cDNAs that detect deletions in …
[引用][C] An 11 base pair duplication in exon 6 of the SMN gene produces a type I spinal muscular atrophy (SMA) phenotype: further evidence for SMN as the primary …
DW Parsons, PE McAndrew, UR Monani… - Human Molecular …, 1996 - elibrary.ru
[PDF][PDF] An 11 base pair duplication in exon 6 of the SMN gene produces a type I spinal muscular atrophy (SMA) phenotype: further evidence for SMN as the primary …
DW Parsons, PE McAndrew, UR Monani… - Human Molecular …, 1996 - researchgate.net
The gene for autosomal recessive spinal muscular atrophy (SMA) has been mapped to 5q12
in a region that contains repeated markers and genes. Three cDNAs that detect deletions in …
in a region that contains repeated markers and genes. Three cDNAs that detect deletions in …
An 11 base pair duplication in exon 6 of the SMN gene produces a type I spinal muscular atrophy (SMA) phenotype: Further evidence for SMN as the primary SMA …
DW Parsons, PE McAndrew… - Human Molecular …, 1996 - ohiostate.elsevierpure.com
The gene for autosomal recessive spinal muscular atrophy (SMA) has been mapped to 5q12
in a region that contains repeated markers and genes. Three cDNAs that detect deletions in …
in a region that contains repeated markers and genes. Three cDNAs that detect deletions in …
[PDF][PDF] An 11 base pair duplication in exon 6 of the SMN gene produces a type I spinal muscular atrophy (SMA) phenotype: further evidence for SMN as the primary …
DW Parsons, PE McAndrew, UR Monani… - Human Molecular …, 1996 - scholar.archive.org
The gene for autosomal recessive spinal muscular atrophy (SMA) has been mapped to 5q12
in a region that contains repeated markers and genes. Three cDNAs that detect deletions in …
in a region that contains repeated markers and genes. Three cDNAs that detect deletions in …
An 11 base pair duplication in exon 6 of the SMN gene produces a type I spinal muscular atrophy (SMA) phenotype: Further evidence for SMN as the primary SMA …
DW Parsons, PE McAndrew… - Human molecular …, 1996 - pure.johnshopkins.edu
The gene for autosomal recessive spinal muscular atrophy (SMA) has been mapped to 5q12
in a region that contains repeated markers and genes. Three cDNAs that detect deletions in …
in a region that contains repeated markers and genes. Three cDNAs that detect deletions in …
[引用][C] An 11 base pair duplication in exon 6 of the SMN gene produces a type I spinal muscular atrophy (SMA) phenotype: further evidence for SMN as the primary …
DW PARSONS, PE MCANDREW… - Human molecular …, 1996 - pascal-francis.inist.fr
An 11 base pair duplication in exon 6 of the SMN gene produces a type I spinal muscular
atrophy (SMA) phenotype : further evidence for SMN as the primary SMA-determining gene …
atrophy (SMA) phenotype : further evidence for SMN as the primary SMA-determining gene …
An 11 base pair duplication in exon 6 of the SMN gene produces a type I spinal muscular atrophy (SMA) phenotype: further evidence for SMN as the primary SMA …
DW Parsons, PE McAndrew, UR Monani… - Human Molecular …, 1996 - europepmc.org
The gene for autosomal recessive spinal muscular atrophy (SMA) has been mapped to 5q12
in a region that contains repeated markers and genes. Three cDNAs that detect deletions in …
in a region that contains repeated markers and genes. Three cDNAs that detect deletions in …