Pediatrics
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18 february 2019 21:01:57 |
| A de novo ANK1 mutation associated to hereditary spherocytosis: a case report (BMC Pediatrics) |
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Tweet Hereditary spherocytosis (HS) is a type of hemolytic anemia caused by abnormal red cell membrane skeletal proteins with few unique clinical manifestations in the neonate and infant. An ANK1 gene mutation is the m... |
| 66 viewsCategory: Pediatrics |
 Anthropometric and clinical correlates of fat mass in healthy term infants at 6 months of age (BMC Pediatrics)Hb Knossos (HBB: c.82G > T), ?-globin CD 5 (-CT) (HBB: c.17_18delCT) and ?-globin CD 59 (-a) (HBD: c.179delA) mutations in a Syrian patient with ?-thalassemia intermedia (BMC Pediatrics) 
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