A modified MS-PCR approach to diagnose patients with Prader-Willi and Angelman syndrome

Screening of UBE3A gene in patients referred for Angelman Syndrome

(2013) Evmorfia Tzagkaraki et al.   EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY

A new approach to touch down method using betaine as co-solvent for increased specificity and intensity of GC rich gene amplification

(2012) Daliparthy D. Pratyush et al.   GENE

Prader-Willi syndrome

(2012) Suzanne B. Cassidy et al.   GENETICS IN MEDICINE

Practice guidelines for the molecular analysis of Prader-Willi and Angelman syndromes

(2010) Simon C Ramsden et al.   BMC Medical Genetics

A Unified Rapid PCR Method for Detection of Normal and Expanded Trinucleotide Alleles of CAG Repeats in Huntington Chorea and CGG Repeats in Fragile X Syndrome

(2010) Tihomir Todorov et al.   MOLECULAR BIOTECHNOLOGY

A Rapid Polymerase Chain Reaction-Based Screening Method for Identification of All Expanded Alleles of the Fragile X (FMR1) Gene in Newborn and High-Risk Populations

(2007) Flora Tassone et al.   JOURNAL OF MOLECULAR DIAGNOSTICS