Phenotype-karyotype correlations in dup(18q): Report of a case and review
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Reference14 articles.
1. Familial mental retardation in a family with an inherited chromosome rearrangement
2. Partial trisomy 18q in a newborn with typical 18 trisomy phenotype
3. Partial trisomy 18q12, due to intrachromosomal duplication, is not associated with typical 18 trisomy phenotype
4. (1971) “Human Cytogenetics.” New York: Academic Press Inc., Vol. II, pp 276-292.
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1. Prenatal molecular cytogenetic analysis of a mild dysmorphic fetus with a huge unbalance karyotype involving partial 9p deletion and partial 18q duplication;Genes & Genomics;2015-10-12
2. Genetic and molecular analysis of a new unbalanced X;18 rearrangement: localization of the diminished ovarian reserve disease locus in the distal Xq POF1 region;Human Reproduction;2011-08-22
3. Prenatal detection of short arm deletion and isochromosome 18 formation investigated by molecular techniques.;Journal of Medical Genetics;1995-12-01
4. Congenital Polyvalvular Cardiac Disease Without Chromosomal Abnormalities;Pediatric Pathology & Laboratory Medicine;1995-01
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