Prenatal diagnosis and carrier detection in primary immunodeficiency disorders.
作者信息
Lau Y L, Levinsky R J
机构信息
Department of Immunology, Institute of Child Health, London.
出版信息
Arch Dis Child. 1988 Jul;63(7 Spec No):758-64. doi: 10.1136/adc.63.7_spec_no.758.
Abstract
摘要
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1
Gene action in the X-chromosome of the mouse (Mus musculus L.).小鼠（小家鼠）X染色体上的基因作用。
Nature. 1961 Apr 22;190:372-3. doi: 10.1038/190372a0.
2
X-linked inheritance in females with chronic granulomatous disease.患有慢性肉芽肿病女性的X连锁遗传
J Clin Invest. 1980 Aug;66(2):332-40. doi: 10.1172/JCI109861.
3
Discoid lupus erythematosus-like lesions and stomatitis in female carriers of X-linked chronic granulomatous disease.X连锁慢性肉芽肿病女性携带者的盘状红斑狼疮样皮损和口腔炎
Br J Dermatol. 1981 May;104(5):495-505. doi: 10.1111/j.1365-2133.1981.tb08163.x.
4
Fungal infection in chronic granulomatous disease. The importance of the phagocyte in defense against fungi.慢性肉芽肿病中的真菌感染。吞噬细胞在抗真菌防御中的重要性。
Am J Med. 1981 Jul;71(1):59-66. doi: 10.1016/0002-9343(81)90259-x.
5
X-linked lymphoproliferative syndrome registry report.X连锁淋巴增殖性综合征登记报告。
J Pediatr. 1980 Apr;96(4):669-73. doi: 10.1016/s0022-3476(80)80735-9.
6
Prenatal diagnosis of ataxia telangiectasia.共济失调毛细血管扩张症的产前诊断
J Pediatr. 1982 Jan;100(1):134-7. doi: 10.1016/s0022-3476(82)80253-9.
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Phenotypic analysis of fetal blood leucocytes: potential for prenatal diagnosis of immunodeficiency disorders.胎儿血白细胞的表型分析：免疫缺陷疾病产前诊断的潜力
Prenat Diagn. 1982 Jul;2(3):211-8. doi: 10.1002/pd.1970020310.
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