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Array Comparative Genomic Hybridization (Array CGH) for Detection of Genomic Copy Number Variants
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Second reported patient with del(1)(p32.1p32.3) and similar clinical features suggesting a recognizable chromosomal

Samuel H Zinner1, Jacqueline R Batanian

  • 1Department of Pediatrics, Division of Developmental Pediatrics, Saint Louis University, St. Louis, Missouri, USA. SZinner@u.washington.edu

American Journal of Medical Genetics. Part A
|September 5, 2003
PubMed

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