Additional case of an uncommon 22q11.2 reciprocal rearrangement in a phenotypically normal mother of children with 22q11.2 deletion and 22q11.2 duplication syndromes
- PMID: 22987734
- DOI: 10.1002/ajmg.a.35595
Additional case of an uncommon 22q11.2 reciprocal rearrangement in a phenotypically normal mother of children with 22q11.2 deletion and 22q11.2 duplication syndromes
Comment on
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Genetic dosage compensation in a family with velo-cardio-facial/DiGeorge/22q11.2 deletion syndrome.Am J Med Genet A. 2011 Mar;155A(3):548-54. doi: 10.1002/ajmg.a.33861. Epub 2011 Feb 18. Am J Med Genet A. 2011. PMID: 21337693 Free PMC article.
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