Similar articles for PMID: 1351407

Year	Number of Results
1919	1
1921	1
1979	1
1986	4
1987	4
1988	9
1989	2
1990	10
1991	3
1992	6
1993	2
1994	2
1995	1
1996	1
1997	1
1998	4
1999	4
2001	3
2003	1
2004	4
2005	3
2006	4
2007	1
2008	2
2013	1
2014	1
2024	0

1

The inheritance of type I and type III von Willebrand's disease in Israel: linkage analysis, carrier detection and prenatal diagnosis using three intragenic restriction fragment length polymorphisms.

Inbal A, Kornbrot N, Zivelin A, Shaklai M, Seligsohn U. Inbal A, et al. Blood Coagul Fibrinolysis. 1992 Apr;3(2):167-77. Blood Coagul Fibrinolysis. 1992. PMID: 1351407

2

Germline de novo mutations and linkage markers vs. DNA sequencing for carrier detection in von Willebrand disease.

Ahmad F, Oyen F, Jan R, Budde U, Schneppenheim R, Saxena R. Ahmad F, et al. Haemophilia. 2014 Jul;20(4):e311-7. doi: 10.1111/hae.12441. Epub 2014 Apr 8. Haemophilia. 2014. PMID: 24712919

3

Prenatal diagnosis of β-thalassemia in twin pregnancies in Iran.

Kainimoghaddam Z, Valaei A, Bayat F, Taghavi Basmanj M, Navabmoghaddam F, Mortezazadeh M, Teimoori-Toolabi L, Ahmadi S, Sadegh S, Kordafshari A, Karimipoor M, Zeinali S. Kainimoghaddam Z, et al. Arch Iran Med. 2013 Oct;16(10):573-5. Arch Iran Med. 2013. PMID: 24093136

4

Use of Intron 40 VNTR I in vWD Gene Tracking.

Enayat MS, Surdhar GK. Enayat MS, et al. Methods Mol Med. 1999;31:179-86. doi: 10.1385/1-59259-248-1:179. Methods Mol Med. 1999. PMID: 21340994

5

The molecular analysis of von Willebrand disease: a guideline from the UK Haemophilia Centre Doctors' Organisation Haemophilia Genetics Laboratory Network.

Keeney S, Bowen D, Cumming A, Enayat S, Goodeve A, Hill M; UK Haemophilia Centre Doctors' Organisation (UKHCDO). Keeney S, et al. Haemophilia. 2008 Sep;14(5):1099-111. doi: 10.1111/j.1365-2516.2008.01813.x. Epub 2008 Jul 14. Haemophilia. 2008. PMID: 18637846

6

The use of DNA markers for carrier detection and prenatal diagnosis of haemophilia A in Egyptian families.

Hussein IR, El-Beshlawy A, Salem A, Mosaad R, Zaghloul N, Ragab L, Fayek H, Gaber K, El-Ekiabi M. Hussein IR, et al. Haemophilia. 2008 Sep;14(5):1082-7. doi: 10.1111/j.1365-2516.2008.01779.x. Epub 2008 Jun 28. Haemophilia. 2008. PMID: 18547262

7

A NEW TYPE OF INHERITANCE.

Castle WE. Castle WE. Science. 1921 Apr 8;53(1371):339-42. doi: 10.1126/science.53.1371.339. Science. 1921. PMID: 17783696 No abstract available.

8

Molecular analysis and prenatal prediction of spinal muscular atrophy in Chinese patients by the combination of restriction fragment length polymorphism analysis, denaturing high-performance liquid chromatography, and linkage analysis.

Chen WJ, Wu ZY, Lin MT, Su JF, Lin Y, Murong SX, Wang N. Chen WJ, et al. Arch Neurol. 2007 Feb;64(2):225-31. doi: 10.1001/archneur.64.2.225. Arch Neurol. 2007. PMID: 17296838

9

Studies on Inheritance in Pigeons. III. Description and Linkage Relations of Two Sex-Linked Characters.

Cole LJ, Kelley FJ. Cole LJ, et al. Genetics. 1919 Mar;4(2):183-203. doi: 10.1093/genetics/4.2.183. Genetics. 1919. PMID: 17245921 Free PMC article. No abstract available.

10

Diagnosis of inherited von Willebrand disease: a clinical perspective.

Federici AB. Federici AB. Semin Thromb Hemost. 2006 Sep;32(6):555-65. doi: 10.1055/s-2006-949661. Semin Thromb Hemost. 2006. PMID: 16977566 Free article. Review.

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