The Prader-Willi-like phenotype in fragile X patients: a designation facilitating clinical (and molecular) differential diagnosis.
作者信息
De Vries B B, Niermeijer M F
出版信息
J Med Genet. 1994 Oct;31(10):820. doi: 10.1136/jmg.31.10.820.
Abstract
摘要
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The Prader-Willi-like phenotype in fragile X patients: a designation facilitating clinical (and molecular) differential diagnosis.脆性X综合征患者中的普拉德-威利样表型：一种有助于临床（及分子）鉴别诊断的命名。
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本文引用的文献
1
Clinical and molecular studies in fragile X patients with a Prader-Willi-like phenotype.具有普拉德-威利样表型的脆性X综合征患者的临床和分子研究。
J Med Genet. 1993 Sep;30(9):761-6. doi: 10.1136/jmg.30.9.761.
2
Clinical and molecular studies in fragile X patients with a Prader-Willi-like phenotype.具有普拉德-威利样表型的脆性X患者的临床和分子研究。
J Med Genet. 1994 Mar;31(3):260-1. doi: 10.1136/jmg.31.3.260-b.
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