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Items: 1 to 20 of 168

1.

[Molecular analysis of two pedigrees with inherited coagulation factor VII deficiency].

Liang WL, Wei HY, Lin FQ, Zhou JL.

Zhonghua Er Ke Za Zhi. 2012 Nov;50(11):817-20. Chinese.

PMID:
23302610
2.

[Genotype and phenotype analysis of congenital coagulator factor VII deficiency in four Chinese pedigrees].

Jiang MH, Wang ZY, Yu ZQ, Bai X, Cao LJ, Su J, Sun XH, Zhang W, Ruan CG.

Zhonghua Xue Ye Xue Za Zhi. 2011 Mar;32(3):147-52. Chinese.

PMID:
21535950
3.

[Novel double heterozygous mutations on Met306Val and Thr181Asn related to a hereditary coagulation factor VII deficiency].

Tu CQ, Deng CY, Wu JZ, Pan CY, Xie CY.

Zhonghua Yi Xue Za Zhi. 2006 Jan 10;86(2):124-7. Chinese.

PMID:
16620721
4.

[Studies on inherited coagulation factor VII deficiency and tissue factor abnormality in a pedigree].

Ding QL, Wang XF, Xu GQ, Huang XP, Hu YQ, Wu WM, Fu QH, Wang HL, Wang ZY.

Zhonghua Xue Ye Xue Za Zhi. 2006 Mar;27(3):150-3. Chinese.

PMID:
16792912
5.

[Gene analysis of a combined inherited factor VII and factor X deficiency pedigree].

Wang MS, Jin YH, Zheng FX, Xie HX, Xu PF, Niu ZZ.

Zhonghua Xue Ye Xue Za Zhi. 2011 Dec;32(12):854-7. Chinese.

PMID:
22339961
6.

[Molecular genetic analysis for a pedigree with severe hereditary coagulation factor VII deficiency].

Ding QL, Wang HL, Wang XF, Wang MS, Fu QH, Wu WM, Hu YQ, Wang ZY.

Zhonghua Nei Ke Za Zhi. 2003 Oct;42(10):692-6. Chinese.

PMID:
14633462
7.

[Analysis of an inherited FVII deficiency pedigree caused by homozygosity of Thr359Met].

Chu HY, Wang HL, Ding QL, Wang XF, Qu B, Wu F, Kang WY, Duan BH, Yin J, Fu QH, Wu WM, Wang ZY.

Zhonghua Xue Ye Xue Za Zhi. 2003 Mar;24(3):134-7. Chinese.

PMID:
12697124
8.

[Phenotype and genotype analysis for a consanguineous pedigree with combined coagulation factor VII and X deficiency].

Jin Y, Wang M, Wang Y, Yang X, Yang L, Xie Y, Xie H, Zhu L, Yu F.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014 Feb;31(1):16-20. doi: 10.3760/cma.j.issn.1003-9406.2014.01.004. Chinese.

PMID:
24510554
9.

[Two novel mutations in one pedigree with hereditary Factor VII deficiency].

Xing ZF, Wang XF, Dai J, Lu YL, Xu GQ, Xi XD, Wang HL.

Zhonghua Xue Ye Xue Za Zhi. 2011 Mar;32(3):158-62. Chinese.

PMID:
21535952
10.

[Molecular genetics and clinical features of nine patients with inherited coagulation factor VII deficiency].

Jin YH, Wang MS, Zheng FX, Xie YS, Xie HX, Xu PF.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012 Aug;29(4):404-7. doi: 10.3760/cma.j.issn.1003-9406.2012.04.006. Chinese.

PMID:
22875495
11.

Twenty two novel mutations of the factor VII gene in factor VII deficiency.

Wulff K, Herrmann FH.

Hum Mutat. 2000;15(6):489-96.

PMID:
10862079
12.

Hereditary factor VII deficiency in the Alaskan Klee Kai dog.

Kaae JA, Callan MB, Brooks MB.

J Vet Intern Med. 2007 Sep-Oct;21(5):976-81.

13.

Exclusion of the first EGF domain of factor VII by a splice site mutation causes lethal factor VII deficiency.

McVey JH, Boswell EJ, Takamiya O, Tamagnini G, Valente V, Fidalgo T, Layton M, Tuddenham EG.

Blood. 1998 Aug 1;92(3):920-6.

14.

[Genetic analysis of a pedigree with hereditary coagulation factor Ⅶ deficiency].

Jin Y, Wang Y, Hao X, Yang L, Xie H, Zhu L, Yu F, Yang X, Wang M.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2015 Apr;32(2):222-5. doi: 10.3760/cma.j.issn.1003-9406.2015.02.015. Chinese.

PMID:
25863091
15.

A novel missense mutation close to the charge-stabilizing system in a patient with congenital factor VII deficiency.

Jiang M, Wang Z, Yu Z, Bai X, Su J, Cao L, Zhang W, Ruan C.

Blood Coagul Fibrinolysis. 2011 Jun;22(4):264-70. doi: 10.1097/MBC.0b013e3283447388.

PMID:
21372693
16.

A novel missense mutation responsible for factor VII deficiency in research Beagle colonies.

Callan MB, Aljamali MN, Margaritis P, Griot-Wenk ME, Pollak ES, Werner P, Giger U, High KA.

J Thromb Haemost. 2006 Dec;4(12):2616-22. Epub 2006 Sep 8.

17.

Detection of missense mutations by single-strand conformational polymorphism (SSCP) analysis in five dysfunctional variants of coagulation factor VII.

Takamiya O, Kemball-Cook G, Martin DM, Cooper DN, von Felten A, Meili E, Hann I, Prangnell DR, Lumley H, Tuddenham EG, et al.

Hum Mol Genet. 1993 Sep;2(9):1355-9.

PMID:
8242057
18.

Two novel mutations in severe factor VII deficiency.

Gomez K, Laffan MA, Kemball-Cook G, Pasi J, Layton M, Singer JD, Tuddenham EG, McVey JH.

Br J Haematol. 2004 Jul;126(1):105-10.

PMID:
15198740
19.

Factor VII R110C: a novel missense mutation (Arg110Cys) in the second epidermal growth factor-like domain causing factor VII deficiency in members of a Japanese family.

Suto M, Uchiumi H, Tsukamoto N, Nojima Y, Tamura J, Naruse T.

Blood Coagul Fibrinolysis. 2000 Jul;11(5):415-9.

PMID:
10937801
20.

Japanese family with congenital factor VII deficiency.

Sakakibara K, Okayama Y, Fukushima K, Kaji S, Muraoka M, Arao Y, Shimada A.

Pediatr Int. 2015 Oct;57(5):1023-4. doi: 10.1111/ped.12696. Epub 2015 Aug 26.

PMID:
26310716

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