Search Results - "Pihko, S. Helena"

18q− Syndrome: Brain MRI shows poor differentiation of gray and white matter on T2-weighted images by Linnankivi, Tarja T., Autti, Taina H., Pihko, S. Helena, Somer, Mirja S., Tienari, Pentti J., Wirtavuori, Kari O., Valanne, Leena K.

“…Purpose To study brain MRI findings in patients with 18q− syndrome and to correlate these findings with the results of the molecular breakpoint analysis…”
Get full text

Usefulness of chromosome 19 RFLP haplotypes in the diagnosis of myotonic dystrophy by Nokelainen, P T, Alanen-Kurki, L, Somer, H V, Pihko, S H, Peltonen, L

“…Three DNA probes (APOC2, PSC11, and LDR152) detecting RFLP polymorphisms were used to test the usefulness of the RFLP approach in myotonic dystrophy (MD)…”
Get more information