Neonatal hyperinsulinemic hypoglycemia in a patient with 9p deletion syndrome
Author:
Funder
Wellcome Trust
Publisher
Elsevier BV
Subject
Genetics(clinical),Genetics,General Medicine
Reference23 articles.
1. Deletion of the short arm of chromosome no.9 (46,9p-): a new deletion syndrome;Alfi;Ann. Genet.,1973
2. Case report. Familial balanced translocation leading to an offspring with phenotypic manifestations of 9p syndrome;Abreu;Genet. Mol. Res.,2014
3. Prevalence and predictors of perinatal hemorrhagic stroke: results from the kaiser pediatric stroke study;Armstrong-Wells;Pediatrics,2009
4. Maternal and infant characteristics associated with perinatal arterial stroke in the preterm infant;Benders;Stroke,2007
5. Nonketotic hyperglycinemia in a patient with the 9p- syndrome;Burton;Am. J. Med. Genet.,1989
Cited by 4 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Insights into the Cardiac Phenotype in 9p Deletion Syndrome: A Multicenter Italian Experience and Literature Review;Genes;2023-01-05
2. Chromosome 9p terminal deletion in nine Egyptian patients and narrowing of the critical region for trigonocephaly;Molecular Genetics & Genomic Medicine;2021-10-05
3. Refinement of the critical genomic region for congenital hyperinsulinism in the Chromosome 9p deletion syndrome;Wellcome Open Research;2020-08-04
4. Refinement of the critical genomic region for hypoglycaemia in the Chromosome 9p deletion syndrome;Wellcome Open Research;2019-10-08
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