X linked mental retardation.
作者信息
Glass I A
机构信息
West Midlands Regional Clinical Genetics Service, Birmingham Maternity Hospital, Edgbaston.
出版信息
J Med Genet. 1991 Jun;28(6):361-71. doi: 10.1136/jmg.28.6.361.
Abstract
摘要
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Evaluation of familial biochemically determined mental retardation in children, with special reference to aminoaciduria.儿童家族性生化测定智力迟钝的评估，特别提及氨基酸尿症。
N Engl J Med. 1960 Mar 31;262:658-65. doi: 10.1056/NEJM196003312621305.
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THE OCULO-CEREBRO-RENAL SYNDROME OF LOWE.
Am J Dis Child. 1965 Mar;109:185-203. doi: 10.1001/archpedi.1965.02090020187001.
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HEREDITARY PARTIAL AGENESIS OF CORPUS CALLOSUM; BIOCHEMICAL AND PATHOLOGICAL STUDIES.遗传性胼胝体部分发育不全；生物化学与病理学研究。
Arch Neurol. 1964 Aug;11:198-208. doi: 10.1001/archneur.1964.00460200094009.
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The syndrome of sex-linked hydrocephalus.性连锁脑积水综合征
Arch Dis Child. 1961 Oct;36(189):486-93. doi: 10.1136/adc.36.189.486.
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An X-linked, recessively inherited syndrome characterized by grave mental deficiency, epilepsy, and endocrine disorder.一种X连锁隐性遗传综合征，其特征为严重智力缺陷、癫痫和内分泌紊乱。
Acta Med Scand. 1962 Jan;171:13-21. doi: 10.1111/j.0954-6820.1962.tb04162.x.
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Aarskog's syndrome.
Arch Dis Child. 1980 Sep;55(9):706-10. doi: 10.1136/adc.55.9.706.
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Fragile X-linked mental retardation: the Martin-Bell syndrome.脆性X连锁智力障碍：马丁-贝尔综合征。
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