Diagnostic and genetical aspects of tuberous sclerosis.
作者信息
Nevin N C, Pearce W G
出版信息
J Med Genet. 1968 Dec;5(4):273-80. doi: 10.1136/jmg.5.4.273.
Abstract
摘要
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本文引用的文献
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DEPIGMENTED NEVI: THE EARLIEST SIGN OF TUBEROUS SCLEROSIS.
Pediatrics. 1965 Jun;35:1003-5.
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Internal manifestations of tuberous sclerosis.
Arch Dermatol. 1963 Jun;87:715-28. doi: 10.1001/archderm.1963.01590180043009.
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Congenital neurocutaneous syndromes in childhood.
J Pediatr. 1959 Oct;55:447-59. doi: 10.1016/s0022-3476(59)80282-1.
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Apert's syndrome (a type of acrocephalosyndactyly)-observations on a British series of thirty-nine cases.阿佩尔综合征（一种尖头并指畸形）——对英国39例病例的观察
Ann Hum Genet. 1960 May;24:151-64. doi: 10.1111/j.1469-1809.1959.tb01728.x.
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Marfan's syndrome in Northern Ireland; an account of thirteen families.
Ann Hum Genet. 1958 Jul;22(4):289-309. doi: 10.1111/j.1469-1809.1958.tb01423.x.
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Achondroplasia: an account of the condition in Northern Ireland.软骨发育不全：北爱尔兰地区该病症的情况说明
Am J Hum Genet. 1957 Mar;9(1):81-91.
7
Frequency of epiloia in Northern Ireland.北爱尔兰结节性硬化症的发病率
Br J Prev Soc Med. 1956 Jul;10(3):134-5. doi: 10.1136/jech.10.3.134.
8
Glial tumors of the retina; in relation to tuberous sclerosis.
Am J Ophthalmol. 1956 Mar;41(3):428-32. doi: 10.1016/0002-9394(56)91258-2.
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Pulmonary tuberous sclerosis and its relationship to other forms of the disease.
Q J Med. 1954 Apr;23(90):113-45.
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Tuberous cerebral sclerosis of Bourneville.
Ophthalmologica. 1952 Dec;124(6):321-39. doi: 10.1159/000301320.
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