Partial trisomy 13q identified by sequential fluorescence in situ hybridization
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference8 articles.
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5. Neurological aspects of del(1q) syndrome
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1. Identification of partial trisomy 13q in two unrelated patients using single-nucleotide polymorphism array and literature overview;Molecular Cytogenetics;2022-07-28
2. Prenatal diagnosis and molecular cytogenetic characterization of a mosaic derivative Y chromosome derived from a de novo unbalanced reciprocal Yq;13q translocation;Taiwanese Journal of Obstetrics and Gynecology;2011-09
3. Primary Massage Using One-Finger Twining Manipulation for Treatment of Infantile Muscular Torticollis;The Journal of Alternative and Complementary Medicine;2011-03
4. Prenatal diagnosis of a partial trisomy 13q (q14→qter): phenotype, cytogenetics and molecular characterization by spectral karyotyping and array comparative genomic hybridization;Genetics and Molecular Research;2010
5. A 14-Year Follow-Up of a Case Detected Prenatally of Partial Trisomy 13q21.32-qter and Monosomy 18q22.3-qter as a Result of a Maternal Complex Chromosome Rearrangement Involving Chromosomes 6, 13, and 18;Genetic Testing and Molecular Biomarkers;2009-06
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