相关参考文献
注意：仅列出部分参考文献，下载原文获取全部文献信息。Chromosome 19p13.3 deletion in a child with Peutz-Jeghers syndrome, congenital heart defect, high myopia, learning difficulties and dysmorphic features: Clinical and molecular characterization of a new contiguous gene syndrome
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G. Bermano et al.
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High proportion of large genomic STK11 deletions in Peutz-Jeghers syndrome
S Aretz et al.
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HL Archer et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2005)
Complete germline deletion of the STK11 gene in a family with Peutz-Jeghers syndrome
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EUROPEAN JOURNAL OF HUMAN GENETICS (2004)
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