18p deletion syndrome with a 45, XY, t (14; 18) (p11;q11.2), -18, karyotype
Author:
Publisher
Elsevier BV
Subject
Genetics
Reference8 articles.
1. Characterization of denove unbalanced translocation t (14q 18q) using microdissection and fluorescence insitu hybridization;Engleen;Am J Med. Genet.,1986
2. The 18p syndrome. Report of four cases;Faust;Europ. J. P,1976
3. 18p- syndrome in mother and daughter;Fryns;Europ. J. P,1979
4. 18p- syndrome resulting from 14q / 18q dicentric fusion tranlocation;Funderbank;Hum Genet,1977
5. The phenotype of a 45,X male with a Y/18 translocation;Gimelli;Clin. Genet,1996
Cited by 5 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. 18p Deletion Syndrome With a 45, XY, t (14;18) (p11.1; p11.1), Karyotype;Cureus;2024-03-05
2. A case of de novo 18p deletion syndrome with panhypopituitarism;Annals of Pediatric Endocrinology & Metabolism;2019-03-31
3. Genotype-Phenotype Analysis, Neuropsychological Assessment, and Growth Hormone Response in a Patient with 18p Deletion Syndrome;Cytogenetic and Genome Research;2018
4. Epilepsy and chromosome 18 abnormalities: A review;Seizure;2015-11
5. Chromosome 18 aberrations and epilepsy: A review;American Journal of Medical Genetics Part A;2005
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