Molecular cytogenetic characterization of a constitutional, highly complex intrachromosomal rearrangement of chromosome 1, with 14 breakpoints and a 0.5 Mb submicroscopic deletion
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
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2. Prenatal Diagnosis of 2q32 Deletion Syndrome Characterized by Multiple Segmental Deletions and Complex Chromosomal Rearrangement Involving Chromosomes 2, 5 and 7;Fetal Diagnosis and Therapy;2012
3. Characterizing complex structural variation in germline and somatic genomes;Trends in Genetics;2012-01
4. Complex X chromosome rearrangement delineated by array comparative genome hybridization in a woman with premature ovarian insufficiency;Fertility and Sterility;2011-06
5. Balanced Reciprocal Translocations Detected at Amniocentesis;Taiwanese Journal of Obstetrics and Gynecology;2010-12
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