Adjacent-2 disjunction of a maternal t(9;22) leading to duplication 9pter→q22 and deficiency of 22pter→q11.2
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference20 articles.
1. Di George syndrome and 22q11 rearrangements
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3. Trisomy 9q?. A variant of the 9p trisomy syndrome
4. Prospective risk in reciprocal translocation heterozygotes at amniocentesis as determined by potential chromosome imbalance sizes. Data of the european collaborative prenatal diagnosis centres
5. A deletion in chromosome 22 can cause digeorge syndrome
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1. A Systematic Review of Reproductive Counseling in Cases of Parental Constitutional Reciprocal Translocation (9;22) Mimicking BCR-ABL1;Frontiers in Genetics;2022-08-04
2. De novo Unbalanced 1;22 Translocation with 22q11 Deletion Syndrome;Cytogenetic and Genome Research;2019
3. Constitutional chromosome rearrangements that mimic the 2017 world health organization “acute myeloid leukemia with recurrent genetic abnormalities”: A study of three cases and review of the literature;Cancer Genetics;2019-01
4. t(9;22)(q34;q11.2) is a recurrent constitutional non-Robertsonian translocation and a rare cytogenetic mimic of chronic myeloid leukemia;Cancer Genetics;2011-10
5. Paternal balanced reciprocal translocation t(9;22)(q34.3;q11.2) resulting in an lnfant with features of the 9q subtelomere and the 22q11 deletion syndromes due to 3:1 meiotic segregation and tertiary monosomy;American Journal of Medical Genetics Part A;2009-11
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