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Updated: Aug 12, 2026

Array Comparative Genomic Hybridization (Array CGH) for Detection of Genomic Copy Number Variants
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Array Comparative Genomic Hybridization (Array CGH) for Detection of Genomic Copy Number Variants

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Frontonasal malformation with tetralogy of Fallot associated with a submicroscopic deletion of 22q11

R F Stratton1, R M Payne

  • 1South Texas Genetics Center, San Antonio 78205, USA.

American Journal of Medical Genetics
|March 31, 1997
PubMed

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