Recombinant chromosome 18 resulting from a maternal pericentric inversion
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference8 articles.
1. Partial 18q trisomy and 18p monosomy resulting from a maternal pericentric inversion, inv(18)(p11.2q21.3)
2. A cytogenetic survey of 11,680 newborn infants
3. Abnormalities resulting from a familial pericentric inversion of chromosome 18
4. Duplication-deficiency of chromosome 18, resulting from recombination of a paternal pericentric inversion, with a note for genetic counselling
Cited by 14 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. Cytogenetic, Molecular, and Phenotypic Characterization of a Patient with de novo Derivative Chromosome 18 and Review of the Literature;Cytogenetic and Genome Research;2019
2. A Peruvian Child with 18p-/18q+ Syndrome and Persistent Microscopic Hematuria;Journal of Pediatric Genetics;2017-07-06
3. A boy with partial dup(18q)/del(18p) due to a maternal pericentric inversion: Genotype-phenotype correlation and risk of recombinant chromosomes based on systematic review of the literature;American Journal of Medical Genetics Part A;2016-09-15
4. Recurrent proximal 18p monosomy and 18q trisomy in a family due to a pericentric inversion;American Journal of Medical Genetics Part A;2014-01-29
5. Pericentric inversion of chromosome 18 in parents leading to a phenotypically normal child with segmental uniparental disomy 18;European Journal of Human Genetics;2011-02-16
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