Ring chromosome 18q and jumping translocation 18p in an adult male with hypergonadotrophic hypogonadism
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference33 articles.
1. Growth hormone, suspected gonadotrophin deficiency, and ring 18 chromosome.
2. Meiotic origin of two ring chromosomes 18 in a girl with developmental delay
3. Prenatal diagnosis of a stable de novo centric fission: A case report
4. Centric fission of chromosome No. 4 in the mother of two patients with trisomy 4p
5. Familial centric fission of chromosome 4.
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1. Hypergonadotropic hypogonadism and chromosomal aberrations: clinical heterogeneity and implications on the health of elderly men, case series;BMC Endocrine Disorders;2023-05-17
2. The spectrum of chromosomal translocations in the Arab world: ethnic-specific chromosomal translocations and their relevance to diseases;Chromosoma;2022-07-30
3. De Novo ring chromosome 11 and non-reciprocal translocation of 11p15.3-pter to 21qter in a patient with congenital heart disease;Molecular Cytogenetics;2015-11-09
4. The conundrum of a jumping translocation (JT) in CVS from twins and review of JTs;American Journal of Medical Genetics Part A;2010-10-26
5. Constitutional telomeric dysfunction in an azoospermic male with extensive telomeric association;American Journal of Medical Genetics Part A;2010-08-20
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