Variations in intelligence in phenylktonuria.
作者信息
PARTINGTON M W
出版信息
Can Med Assoc J. 1962 Apr 21;86(16):736-43.
Abstract
摘要
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Polysome immunoprecipitation of phenylalanine hydroxylase mRNA from rat liver and cloning of its cDNA.从大鼠肝脏中对苯丙氨酸羟化酶信使核糖核酸进行多核糖体免疫沉淀及其互补脱氧核糖核酸的克隆。
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本文引用的文献
1
An evaluation of the treatment of phenylketonuria with diets low in phenylalanine.低苯丙氨酸饮食治疗苯丙酮尿症的评估
Pediatrics. 1960 Jul;26:1-11.
2
Atypical phenylketonuria in sisters with normal offspring.
Lancet. 1961 Aug 26;2(7200):464-5. doi: 10.1016/s0140-6736(61)92434-5.
3
The early symptoms of phenylketonuria.苯丙酮尿症的早期症状。
Pediatrics. 1961 Mar;27:465-73.
4
A case of phenylketonuria in the Eta resulting from the mating of a homozygous father and a heterozygous mother.一例因纯合子父亲与杂合子母亲交配导致的埃塔型苯丙酮尿症病例。
Am J Hum Genet. 1961 Mar;13(1 Pt 1):64-8.
5
Results of treatment in phenylketonuria.苯丙酮尿症的治疗结果。
Br Med J. 1961 Mar 18;1(5228):767-71. doi: 10.1136/bmj.1.5228.767.
6
Phenylketonuria. II. Results of treatment of infants and young children. A report of 10 cases.
J Pediatr. 1961 Jul;59:102-18. doi: 10.1016/s0022-3476(61)80217-5.
7
Phenylketonuria with normal intelligence.
Am J Dis Child. 1961 Jul;102:115-22. doi: 10.1001/archpedi.1961.02080010117019.
8
Phenylketonuria treated from earliest infancy; report of three cases.
AMA J Dis Child. 1959 Mar;97(3):345-7. doi: 10.1001/archpedi.1959.02070010347014.
9
Phenylketonuria: the phenylalanine-tyrosine ratio in the detection of the heterozygous carrier.苯丙酮尿症：杂合子携带者检测中的苯丙氨酸 - 酪氨酸比率
J Ment Defic Res. 1958 Jun;2(1):8-16. doi: 10.1111/j.1365-2788.1958.tb00380.x.
10
A one-year, controlled study of the effect of low-phenylalanine diet on phenylketonuria.一项关于低苯丙氨酸饮食对苯丙酮尿症影响的为期一年的对照研究。
Pediatrics. 1958 Feb;21(2):178-202.
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