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See Latest ArticlesMicrocephaly, sensorineural deafness and Currarino triad with duplication-deletion of distal 7q
European Journal of Pediatrics, 10/20/09
Pavone P et al. – The spectrum of associated anomalies in this newly recognised phenotype complex consists of growth failure, typical facial anomalies with additional nervous system abnormalities and somatomedin C deficiency.
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Autoinflammatory diseases in childhood
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Today in Basic Science/Genetics...keeping you current
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Examination of all type 2 diabetes GWAS loci reveals HHEX-IDE as a locus influencing pediatric BMI
Diabetes, 11/25/09
Axenfeld-Rieger ocular anomaly and retinoblastoma caused by constitutional chromosome 13q deletion
Pediatric Blood & Cancer, 11/25/09
The development and piloting of the ISPCAN Child Abuse Screening Tool-Parent version (ICAST-P)
Child Abuse and Neglect, 11/24/09
Today in Pediatric Otolaryngology...keeping you current
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New Patterns in the Otopathogens Causing Acute Otitis Media Six to Eight Years After Introduction of Pneumococcal Conjugate Vaccine
The Pediatric Infectious Disease Journal, 11/25/09
Increasing Importance of Multidrug-Resistant Serotype 6A Streptococcus pneumoniae Clones in Acute Otitis Media in Southern Israel
The Pediatric Infectious Disease Journal, 11/20/09
Vocal cord paralysis in children
Current Opinion in Otolaryngology and Head & Neck Surgery, 11/19/09
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