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See Latest ArticlesImproving Accuracy of Tay Sachs Carrier Screening of the Non Jewish Population: Analysis of 34 Carriers and 6 late-onset Patients with HEXA Enzyme and DNA Sequence Analysis
Pediatric Research, 10/29/09
Park NJ et al. – Gene sequencing, is useful in identifying rare mutations in TSD patients and their families, in evaluating spouses of known carriers for TSD who have indeterminate enzyme analysis and negative for common mutation analysis, and in resolving ambiguous enzyme testing results.
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Why are some children with early onset of asthma getting better over the years? - Diagnostic failure or salutogenetic factors
International Journal of Medical Sciences , 12/04/09
Prevalence of Sexually Transmitted Infections Among Female Adolescents Aged 14 to 19 in the United States
Pediatrics, 12/04/09
Skin-to-Skin Contact and/or Oral 25% Dextrose for Procedural Pain Relief for Term Newborn Infants
Pediatrics, 12/04/09
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