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November 6, 2006Human Mutation

Deletion mapping in Xp21 for patients with complex glycerol kinase deficiency using SNP mapping arrays

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CSChristopher M. StanczakZCZugen ChenYZYao‐Hua Zhang

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Stanczak et al. (2006) studied this question.

synapsesocial.com/papers/6aab3a250d4e9cc1daa53295https://doi.org/10.1002/humu.20424
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  1. 1Homozygous Deletions and Chromosome Amplifications in Human Lung Carcinomas Revealed by Single Nucleotide Polymorphism Array Analysis2005 · 339 citations
  2. 2Rapid detection of submicroscopic chromosomal rearrangements in children with multiple congenital anomalies using high density oligonucleotide arrays2006 · 47 citations