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See Latest ArticlesFGFR3 Gene Mutations in Chinese Cases of Thanatophoric Dysplasia Type 1
Fetal Diagnosis and Therapy, 10/21/09
Yang Y et al. – The results suggest that the R248C mutation may serve as the primarily targeted one of the FGFR3 gene for rapid molecular diagnosis of TD 1.
Today in Basic Science/Genetics...keeping you current
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Neonatal seizures and Long QT Syndrome: A cardiocerebral channelopathy
Epilepsia, 11/10/09
Genetic forms of hypopituitarism and their manifestation in the neonatal period
Early Human Development, 10/30/09
BTNL2 gene polymorphisms may be associated with susceptibility to Kawasaki disease and formation of coronary artery lesions in Taiwanese children
European Journal of Pediatrics, 11/05/09
Today in Epidemiology...keeping you current
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Clinical Presentation of Rheumatic Fever in an Endemic Area
BMJ - Archives of Diseases in Childhood, 11/12/09
Pediatric Burn Injuries Treated in US Emergency Departments Between 1990 and 2006
Pediatrics, 10/30/09
Does BCG vaccination protect against the development of childhood asthma? A systematic review and meta-analysis of epidemiological studies
International Journal of Epidemiology, 10/14/09
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