Ontology highlight
ABSTRACT:
SUBMITTER: Lodder EM
PROVIDER: S-EPMC2759026 | biostudies-literature | 2009
REPOSITORIES: biostudies-literature
Lodder Elisabeth M EM Eussen Bert H BH van Hassel Daniëlla A C M DA Hoogeboom A Jeannette M AJ Poddighe Pino J PJ Coert J Henk JH Oostra Ben A BA de Klein Annelies A de Graaff Esther E
Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology 20090812 6
Apparently balanced chromosomal inversions may lead to disruption of developmentally important genes at the breakpoints of the inversion, causing congenital malformations. Characterization of such inversions may therefore lead to new insights in human development. Here, we report on a de novo inversion of chromosome 7 (p15.2q36.3) in a patient with postaxial polysyndactyly. The breakpoints do not disrupt likely candidate genes for the limb phenotype observed in the patient. However, on the p-arm ...[more]