Reciprocal translocation associated with multiple exostoses in seven members of a three generation family and discovered through an infertile male
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference31 articles.
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1. Hereditary multiple exostoses caused by a chromosomal inversion removing part of EXT1 gene;Molecular Cytogenetics;2023-05-22
2. Olfactory Receptor-Related Duplicons Mediate a Microdeletion at 11q13.2q13.4 Associated with a Syndromic Phenotype;Molecular Syndromology;2010
3. Cryptic deletions are a common finding in "balanced" reciprocal and complex chromosome rearrangements: a study of 59 patients;Journal of Medical Genetics;2007-09-14
4. Familial Robertsonian 13;14 Translocation With Mental Retardation and Epilepsy;Journal of Child Neurology;2006-06
5. Two-color multiplex ligation-dependent probe amplification: Detecting genomic rearrangements in hereditary multiple exostoses;Human Mutation;2004
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