Growth hormone insufficiency associated with haploinsufficiency at 18q23
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Reference25 articles.
1. Galanin—10 years with a neuroendocrine peptide
2. Familial growth hormone deficiency resulting from a 7.6 kb deletion within the growth hormone gene cluster
3. Preferential loss of the paternal alleles in the 18q- syndrome
4. A comprehensive genetic map of the human genome based on 5,264 microsatellites
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1. Genetic analysis and prenatal diagnosis of a pedigree with developmental retardation due to paternal 8q/18q translocation;Clinical Case Reports;2023-12
2. Case report: genetic analysis of a child with 18q deletion syndrome and developmental dysplasia of the hip;BMC Medical Genomics;2022-09-19
3. Clinical Characteristics and Long-Term Recombinant Human Growth Hormone Treatment of 18q- Syndrome: A Case Report and Literature Review;Frontiers in Endocrinology;2021-12-09
4. Subcutaneous immunoglobulin replacement therapy in a patient with 18q deletion syndrome, primary immune deficiency, and type 1 diabetes;International Journal of Immunopathology and Pharmacology;2021-01
5. Short stature in genetic syndromes: Selected issues;Advances in Clinical and Experimental Medicine;2018-03-31
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