Prader-Willi Syndrome Research Today is a free monthly online journal that collates and summarizes the latest research about Prader-Willi Syndrome, including details on pws, symptoms, treatment, causes.

Volume 3 (2007), Issue 10 (October)

1. Albinism and developmental delay: the need to test for 15q11-q13 deletion.
   Pediatr Neurol, 37(4): 299-302. [Abstract] [Full-text]
2. Molecular genetic diagnostics of Prader-Willi Syndrome: a validation of linkage analysis for the Chinese population.
   J Genet Genomics, 34(10): 885-91. [Abstract] [Full-text]
3. Methylation-sensitive high-resolution melting-curve analysis of the SNRPN gene as a diagnostic screen for Prader-Willi and Angelman syndromes.
   Clin Chem, 53(11): 1960-2. [Abstract] [Full-text]
4. Inactivation of the mouse Magel2 gene results in growth abnormalities similar to Prader-Willi syndrome.
   Hum Mol Genet, 16(22): 2713-9. [Abstract] [Full-text]
5. Genotype/phenotype correlations in two patients with 12q subtelomere deletions.
   Am J Med Genet A, 143(22): 2700-5. [Abstract] [Full-text]

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