Coinheritance of Rotor Syndrome, G‐6‐PD Deficiency, and Heterozygous β Thalassemia: A Possible Genetic Interaction-Reference-Cited by-同舟云学术

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Coinheritance of Rotor Syndrome, G‐6‐PD Deficiency, and Heterozygous β Thalassemia: A Possible Genetic Interaction

Published:2001-08 Issue:2 Volume:33 Page:211-213
ISSN:0277-2116
Container-title:Journal of Pediatric Gastroenterology and Nutrition
language:en
Short-container-title:J. pediatr. gastroenterol. nutr.

Author:

Fretzayas Andrew¹,Koukoutsakis Petros¹,Moustaki Maria²,Stavrinadis Christodoulos¹,Karpathios Themistocles¹

Affiliation:

1. Second Department of Pediatrics University of Athens Athens Greece

2. “P & A Kyriakou” Children's Hospital Athens Greece

Publisher

Wiley

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/j.1536-4801.2001.tb07440.x

Reference21 articles.

1. Studies of chronic familial non-hemolytic jaundice with conjugated bilirubin in the serum with and without an unidentified pigment in the liver cells

2. Rotor's syndrome

3. Homozygous haemoglobin O disease and conjugated hyperbilirubinaemia in a Sudanese family.

4. Severe Jaundice in a Gunshot Casualty due to the Coexistence of Dubin-Johnson and Glucose-6-Phosphate Dehydrogenase Deficiency

5. Gilbert's syndrome and jaundice in glucose‐6‐phosphate dehydrogenase deficient neonates;Iolascon A;Haematologica,1999

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