HIGHLIGHTS
- who: Manuel Alejandro Vu00e1squez Salguero et al. from the StudentUniversidad del Valle, Cali, Colombia have published the article: Abstracts, in the Journal: (JOURNAL)
SUMMARY
The phenotype of structural chromosome 18 mutations is highly heterogenous, clinical manifestations may range from mild to severe, they have been widely studied in the literature, however, there are few cases where two or more mutations are present in the same individual, reports where these alterations are caused by a maternal pericentric inversion and diagnosed prenatally are even rarer. Affected individuals are generally characterized by low birth weight, intellectual . . .
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