49,XXXXY syndrome.
作者信息
Pallister P D
出版信息
Am J Med Genet. 1982 Nov;13(3):337-9. doi: 10.1002/ajmg.1320130320.
PMID:7180880
Abstract
摘要
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引用本文的文献
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First Report of Two Rare Entities in a Family: 49,XXXXY and 45,X.
J Pediatr Genet. 2017 Sep;6(3):174-176. doi: 10.1055/s-0037-1598027. Epub 2017 Jan 18.
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49,XXXXY: a distinct phenotype. Three new cases and review.
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Congenital knee dislocation in a 49,XXXXY boy.
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Brief report: a case study of an adolescent male with XXXXY Klinefelter's syndrome.
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