Congenital spherocytosis, B19 parvovirus infection and inherited interstitial deletion of the short arm of chromosome 8
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2141.1991.tb04425.x/fullpdf
Reference33 articles.
1. Inheritance Pattern and Clinical Response to Splenectomy as a Reflection of Erythrocyte Spectrin Deficiency in Hereditary Spherocytosis
2. Partial deficiency of erythrocyte spectrin in hereditary spherocytosis
3. Human Parvovirus Infection in Pregnancy and Hydrops Fetalis
4. Further Evidence for Location of the Spherocytosis Gene on Chromosome 8
5. E. Beutler (1975 )Red Cell Metabolism. A Manual of Biochemical Methods. 2nd edn , p.112 . Grune and Stratton, New York.
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1. Hereditary spherocytosis: review of cases and discussion of hematologic characteristics and updated diagnostic testing;Journal of Advanced Pediatrics and Child Health;2023-03-13
2. Novel 12 Mb interstitial deletion of chromosome 8p11.22-p21.2: a case report;BMC Medical Genomics;2022-06-06
3. Prevalence and Phenotypic Effects of Copy Number Variants in Isolated Hypogonadotropic Hypogonadism;The Journal of Clinical Endocrinology & Metabolism;2022-05-16
4. Global retardation and hereditary spherocytosis associated with a novel deletion of chromosome 8p11.21 encompassing KAT6A and ANK1;European Journal of Medical Genetics;2020-12
5. Human Parvoviruses;Clinical Microbiology Reviews;2017-01
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