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A 11.7-Mb Paracentric Inversion in Chromosome 1q Detected in Prenatal Diagnosis Associated with Familial Intellectual Disability.

作者信息

Rigola Maria A, Baena Neus, Català Vicenç, Lozano Iris, Gabau Elisabet, Guitart Miriam, Fuster Carmen

机构信息

Unitat de Biologia Cel∙lular i Genètica Mèdica, Departament de Biologia Cel∙lular, Fisiologia i Immunologia, Facultat de Medicina, Universitat Autònoma de Barcelona, Bellaterra, Spain.

出版信息

Cytogenet Genome Res. 2015;146(2):109-114. doi: 10.1159/000437127. Epub 2015 Jul 31.

Abstract

Most apparent balanced chromosomal inversions are usually clinically asymptomatic; however, infertility, miscarriages, and mental retardation have been reported in inversion carriers. We present a small family with a paracentric inversion 1q42.13q43 detected in routine prenatal diagnosis. Molecular cytogenetic methods defined the size of the inversion as 11.7 Mb and excluded other unbalanced chromosomal alterations in the patients. Our findings suggest that intellectual disability is caused by dysfunction, disruption, or position effects of genes located at or near the breakpoints involved in this inversion.

摘要

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