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MLPA
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Pitfalls in the detection of gross gene rearrangements using MLPA in Fabry disease.
A summary of molecular genetic findings in fructose-1,6-bisphosphatase deficiency with a focus on a …
Monitoring coal mine changes and their impact on landscape patterns in an alpine region: a case stud…
Major Contribution of Genomic Copy Number Variation in Syndromic Congenital Heart Disease: The Use o…
Assessment of MYCN amplification status in Tunisian neuroblastoma: CISH and MLPA combining approach.
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Markers of Inflammation in Hematopoietic Stem Cell Transplant
Studying Biomarkers in Samples From Younger Patients With Wilms Tumor
Gene Analysis in Studying Susceptibility to Wilms Tumor
Diagnosis of Prader-Willi Syndrome and Angelman Syndrome
Studying Chromosomes in Samples From Younger Patients With Neuroblastoma
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