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1
Genetics of human blood coagulation.人类血液凝固的遗传学
J Med Genet. 1965 Dec;2(4):254-303. doi: 10.1136/jmg.2.4.254.
2
[BLOOD COAGULATION RESEARCH IN 3 CASES OF PTA HEMOPHILIA (CAUSED BY FACTOR XI DEFICIENCY) OF A MAJOR TYPE].3例重型PTA血友病（因子Ⅺ缺乏所致）的血液凝固研究
Haematologica. 1963;48:679-96.
3
[HEREDITARY COAGULOPATHIES].[遗传性凝血障碍]
Med Clin (Barc). 1963 Jul;41:20-3.
4
MACROTHROMBOCYTIC THROMBOPATHIA. CLINICAL, COAGULATION AND HEREDITARY ASPECTS.
Thromb Diath Haemorrh. 1963 Nov 1;10:88-100.
5
[THE BLOOD COAGULATION SYSTEM IN FEMALE CARRIERS OF HEMOPHILIA A AND B].[血友病A和B女性携带者的血液凝固系统]
Pol Arch Med Wewn. 1964;34:165-74.
6
ABNORMAL BLOOD COAGULATION IN CARRIERS OF HEMOPHILIA.血友病携带者的异常血液凝固
J Lab Clin Med. 1964 Apr;63:621-37.
7
BLEEDING DIATHESES IN SURGICAL PATIENTS.外科患者的出血素质
Monogr Surg Sci. 1964 Mar;1:3-57.
8
[STUDY OF NORMAL BLOOD COAGULATION IN TWINS WITH THE THROMBELASTOGRAPHIC METHOD].
Acta Genet Med Gemellol (Roma). 1964 Jan;13:1-19.
9
[PHYSIOLOGIC COAGULATION TESTS IN HETEROZYGOTIC FEMALE HEMOPHILIA CARRIERS].
Schweiz Med Wochenschr. 1965 Mar 6;95:320-5.
10
COAGULATION STUDIES IN HEMOPHILIOID DISEASES: THEIR IMPORTANCE IN TREATMENT PLANNING.血友病类疾病的凝血研究：其在治疗规划中的重要性。
J Oral Surg Anesth Hosp Dent Serv. 1964 Jul;22:324-31.

引用本文的文献

1
Demonstration of a double hereditary pattern for congenital afibrinogenemia.先天性无纤维蛋白原血症的双遗传模式证明。
Blut. 1981 Oct;43(4):249-56. doi: 10.1007/BF00320454.
2
Congenital dysprothrombinemia: an inherited structural disorder of human prothrombin.先天性凝血酶原血症：一种人类凝血酶原的遗传性结构紊乱。
J Clin Invest. 1969 Dec;48(12):2251-9. doi: 10.1172/JCI106191.
3
Heredity in haematology.血液学中的遗传因素。
Proc R Soc Med. 1967 May;60(5):439-48. doi: 10.1177/003591576706000502.
4
The genetic basis of variation in factor 8 levels among haemophiliacs.血友病患者中凝血因子8水平变异的遗传基础。
J Med Genet. 1971 Jun;8(2):136-9. doi: 10.1136/jmg.8.2.136.
5
A report of a case of congenital afibrinogenemia.
Blut. 1972 Jan;24(1):23-31. doi: 10.1007/BF01633139.
6
Variations in levels of blood clotting factors IX and X in a population of normal men: possible genetic polymorphisms.正常男性群体中凝血因子IX和X水平的变化：可能的基因多态性。
Am J Hum Genet. 1972 Mar;24(2):168-80.
7
Congenital combined factor V and factor VIII deficiency in a male born from a brother-sister incest.
Blut. 1974 Jan;28(1):33-42. doi: 10.1007/BF01630657.
8
Congenital factor VII deficiency. A case report.先天性因子VII缺乏症。病例报告。
Blut. 1973 Oct;27(4):236-42. doi: 10.1007/BF01637436.
9
Hemorrhagic varicella in parahemophilia.
Blut. 1972 Nov;25(5):293-301. doi: 10.1007/BF01631811.

本文引用的文献

1
Genetic Considerations in Familial Hemorrhagic Disease. I. The Sex-Linked Recessive Disorders, Hemophilia and PTC Deficiency.家族性出血性疾病的遗传学考量。I. 性连锁隐性疾病、血友病和血浆凝血活酶前体缺乏症。
Am J Hum Genet. 1963 Mar;15(1):53-61.
2
Sex Linkage in Man.人类的性连锁
Genetics. 1930 Sep;15(5):401-44. doi: 10.1093/genetics/15.5.401.
3
HEMOPHILIA. II. SOME PROPERTIES OF A SUBSTANCE OBTAINED FROM NORMAL HUMAN PLASMA EFFECTIVE IN ACCELERATING THE COAGULATION OF HEMOPHILIC BLOOD.血友病。二、从正常人血浆中提取的一种物质的某些特性，该物质能有效加速血友病患者血液的凝固。
J Clin Invest. 1937 Jan;16(1):113-24. doi: 10.1172/JCI100829.
4
[Phase contrast microscopy of the coagulocyte, coagulation islets and the coagulation of plasma in the blood of insects].[昆虫血液中凝血细胞、凝血小岛及血浆凝固的相差显微镜观察]
Experientia. 1950 Aug 15;6(8):297-8. doi: 10.1007/BF02170902.
5
Hemophilia in twins.双胞胎中的血友病
Am J Med. 1949 Dec;7(6):841-3, illust. doi: 10.1016/0002-9343(49)90424-6.
6
Plasma thromboplastin component (PTC) deficiency; a new disease resembling hemophilia.血浆凝血活酶成分（PTC）缺乏症；一种类似血友病的新疾病。
Proc Soc Exp Biol Med. 1952 Apr;79(4):692-4. doi: 10.3181/00379727-79-19488.
7
A familial disorder of blood coagulation due to deficiency of the labile factor.
Q J Med. 1952 Jan;21(81):19-31.
8
The influence of certain drugs on blood coagulation and related phenomena.某些药物对血液凝固及相关现象的影响。
Pharmacol Rev. 1951 Sep;3(3):278-344.
9
Assay of plasma antihemophilic activity in normal heterozygous (hemophilia) and prothrombinopenic dogs.正常杂合子（血友病）犬和凝血酶原缺乏症犬血浆抗血友病活性的测定
Proc Soc Exp Biol Med. 1951 Jun;77(2):294-6. doi: 10.3181/00379727-77-18755.
10
Congenital afibrinogenemia.先天性无纤维蛋白原血症
Br Med J. 1951 Jul 14;2(4723):86-8. doi: 10.1136/bmj.2.4723.86.

Genetics of human blood coagulation.

作者信息

Kerr C B

出版信息

J Med Genet. 1965 Dec;2(4):254-303. doi: 10.1136/jmg.2.4.254.

DOI:10.1136/jmg.2.4.254
PMID:5323610
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1012879/
Abstract
摘要