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1.
Molecular basis of type I antithrombin deficiency in two women with recurrent venous thromboembolism in the first trimester of pregnancy.
Blood Cells Mol Dis
; 48(4): 254-9, 2012 Apr 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-22424603
2.
[Phenotype and genotype analysis of two Chinese pedigrees with type 3 von Willebrand diseases].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 29(5): 524-8, 2012 Oct.
Artículo
en Zh
| MEDLINE | ID: mdl-23042386
3.
[The phenotypic and genotypic diagnosis of three Chinese patients with von Willebrand disease].
Zhonghua Nei Ke Za Zhi
; 51(10): 788-92, 2012 Oct.
Artículo
en Zh
| MEDLINE | ID: mdl-23290978
4.
Hereditary protein C deficiency caused by compound heterozygous mutants in two independent Chinese families.
Pathology
; 46(7): 630-5, 2014 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-25393254
5.
[The binding mechanisms of F VIII Trp1707Ser mutation-associated inhibitor].
Zhonghua Xue Ye Xue Za Zhi
; 34(8): 691-5, 2013 Aug.
Artículo
en Zh
| MEDLINE | ID: mdl-23978021
6.
[Functional study of abnormal fibrinogen caused by Arg275His mutation in fibrinogen γ chain].
Zhonghua Xue Ye Xue Za Zhi
; 34(3): 190-4, 2013 Mar.
Artículo
en Zh
| MEDLINE | ID: mdl-23683413
7.
[The molecular mechanism of haemophilia B caused by the Arg327Ile novel mutation in FIX gene in vitro expression].
Zhonghua Xue Ye Xue Za Zhi
; 33(8): 642-7, 2012 Aug.
Artículo
en Zh
| MEDLINE | ID: mdl-23134860
8.
[Genotype and function analyses of four inherited dysfibrinogenemia pedigree caused by Arg16 amino acid substitution in fibrinogen Aα chain].
Zhonghua Xue Ye Xue Za Zhi
; 33(6): 475-9, 2012 Jun.
Artículo
en Zh
| MEDLINE | ID: mdl-22967385
9.
[Molecular analysis of a patient with hemophilia A caused by FVIII His99Arg mutation].
Zhonghua Xue Ye Xue Za Zhi
; 32(9): 587-91, 2011 Sep.
Artículo
en Zh
| MEDLINE | ID: mdl-22338150
10.
[Two novel mutations in one pedigree with hereditary Factor VII deficiency].
Zhonghua Xue Ye Xue Za Zhi
; 32(3): 158-62, 2011 Mar.
Artículo
en Zh
| MEDLINE | ID: mdl-21535952
11.
[Molecular mechanisms of recurrent venous thrombosis in two pedigrees with type I antithrombin deficiency].
Zhonghua Xue Ye Xue Za Zhi
; 32(12): 848-53, 2011 Dec.
Artículo
en Zh
| MEDLINE | ID: mdl-22339960
12.
[Phenotype and genotype analysis of three Chinese pedigrees with von Willebrand disease].
Zhonghua Xue Ye Xue Za Zhi
; 32(2): 99-102, 2011 Feb.
Artículo
en Zh
| MEDLINE | ID: mdl-21429375
13.
[Analysis of phenotype and genotype in three Chinese pedigrees with inherited dysfibrinogenemia].
Zhonghua Xue Ye Xue Za Zhi
; 32(3): 153-7, 2011 Mar.
Artículo
en Zh
| MEDLINE | ID: mdl-21535951
14.
[Two new mutations of AT gene in type I inherited antithrombin deficiency.].
Zhonghua Xue Ye Xue Za Zhi
; 31(3): 145-8, 2010 Mar.
Artículo
en Zh
| MEDLINE | ID: mdl-20510100
15.
[Analysis of phenotype and genotype in four Chinese pedigrees with inherited coagulation factor V deficiency.].
Zhonghua Xue Ye Xue Za Zhi
; 31(3): 149-53, 2010 Mar.
Artículo
en Zh
| MEDLINE | ID: mdl-20510101
16.
[Detection of factor IX gene mutation in patients with hemophilia B by DNA sequencing].
Zhongguo Shi Yan Xue Ye Xue Za Zhi
; 17(2): 476-8, 2009 Apr.
Artículo
en Zh
| MEDLINE | ID: mdl-19379592
17.
[Gene diagnosis of 3 haemophilia B families].
Zhonghua Xue Ye Xue Za Zhi
; 29(3): 179-82, 2008 Mar.
Artículo
en Zh
| MEDLINE | ID: mdl-18788618
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