Bronchiectasis and immune deficiency in an adult patient with deletion 2q37 due to an unbalanced translocation t(2;10)
Author:
Publisher
Elsevier BV
Subject
Genetics(clinical),Genetics,General Medicine
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1. Prenatal diagnosis of partial monosomy 2q (2q37.3→qter) and partial trisomy 10q (10q24.31→qter) of paternal origin associated with increased nuchal translucency and abnormal maternal serum screening results;Taiwanese Journal of Obstetrics and Gynecology;2020-09
2. Genetic syndromes with evidence of immune deficiency;Stiehm's Immune Deficiencies;2020
3. Primary immunodeficiency associated with chromosomal aberration – an ESID survey;Orphanet Journal of Rare Diseases;2016-08-02
4. Unbalanced Translocations Involving Chromosome Region 10q25.3q26.3 in Patients with Intellectual Disability and Complex Phenotypes;Cytogenetic and Genome Research;2014
5. Genetic Syndromes with Evidence of Immune Deficiency;Stiehm's Immune Deficiencies;2014
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