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Mutation Analysis of the ASPM Gene in 18 Pakistani Families With Autosomal Recessive Primary Microcephaly
Journal of Child Neurology, 10/14/09
Kousar R et al. – Three previously described mutations were also detected in 11 families. These identified mutations extended the body of evidence implicating the ASPM gene in the pathogenesis of human hereditary primary microcephaly.
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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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