Xq chromosome duplication in males: Clinical, cytogenetic and array CGH characterization of a new case and review
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Reference33 articles.
1. Two brothers with multiple congenital anomalies and mental retardation due to disomy (X)(q12 → q13.3) inherited from the mother
2. De novo dup(X)(q22.3q26) in a girl with evidence that functional disomy of X material is the cause of her abnormal phenotype
3. Dir dup(X) (q13→qter) in a girl with growth retardation, microcephaly, developmental delay, seizures, and minor anomalies
4. An interstitial duplication of the X chromosome in a male allows physical fine mapping of probes from the Xq13-q22 region
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3. Xq25 microduplication syndrome: a further contribution to its definition. A case report and review of the literature;Clinical Dysmorphology;2020-04
4. Integrated functional genomic analyses of Klinefelter and Turner syndromes reveal global network effects of altered X chromosome dosage;Proceedings of the National Academy of Sciences;2020-02-18
5. Prenatal Diagnosis of Sex Chromosome Abnormalities;Genetic Disorders and the Fetus;2015-11-23
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