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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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Holiday Ornament-Related Injuries in Children
Pediatric Emergency Care, 12/17/09
Autistic Spectrum Disorders: Assessment and Intervention in Children and Adolescents
British Journal of Medical Practitioners, 12/17/09
Nipple Pain at Presentation Predicts Success of Tongue-Tie Division for Breastfeeding Problems
European Journal of Pediatric Surgery, 12/17/09
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