126 related articles for article (PubMed ID: 1674891)
1. Rapid neonatal diagnosis of type IIB von Willebrand disease using the polymerase chain reaction.
Mannhalter C; Kyrle PA; Brenner B; Lechner K
Blood; 1991 Jun; 77(11):2539-40. PubMed ID: 1674891
[No Abstract] [Full Text] [Related]
2. Polymerase chain reaction amplification of two polymorphic simple repeat sequences within the von Willebrand factor gene: application to family studies in von Willebrand disease.
Cumming AM; Armstrong JG; Pendry K; Burn AM; Wensley RT
Hum Genet; 1992 May; 89(2):194-8. PubMed ID: 1587530
[TBL] [Abstract][Full Text] [Related]
3. Family studies and prenatal diagnosis in severe von Willebrand disease by polymerase chain reaction amplification of a variable number tandem repeat region of the von Willebrand factor gene.
Peake IR; Bowen D; Bignell P; Liddell MB; Sadler JE; Standen G; Bloom AL
Blood; 1990 Aug; 76(3):555-61. PubMed ID: 2378985
[TBL] [Abstract][Full Text] [Related]
4. A de novo mutation in exon 28 of the von Willebrand factor gene in a patient with type IIA von Willebrand's disease coincides with an MboI polymorphism in the von Willebrand factor pseudogene.
Pérez-Casal M; Daly M; Peake I
Hum Mol Genet; 1993 Dec; 2(12):2159-61. PubMed ID: 7906590
[No Abstract] [Full Text] [Related]
5. Family studies in von Willebrand's disease by analysis of restriction fragment length polymorphisms and an intragenic variable number tandem repeat (VNTR) sequence.
Standen GR; Bignell P; Bowen DJ; Peake IR; Bloom AL
Br J Haematol; 1990 Oct; 76(2):242-9. PubMed ID: 1982729
[TBL] [Abstract][Full Text] [Related]
6. Von Willebrand gene tracking by single-tube automated fluorescent analysis of four short tandem repeat polymorphisms.
Vidal F; Julià A; Altisent C; Puig L; Gallardo D
Thromb Haemost; 2005 May; 93(5):976-81. PubMed ID: 15886817
[TBL] [Abstract][Full Text] [Related]
7. Rapid neonatal diagnosis of von Willebrand's disease by use of the polymerase chain reaction.
Bignell P; Standen GR; Bowen DJ; Peake IR; Bloom AL
Lancet; 1990 Sep; 336(8715):638-9. PubMed ID: 1975417
[No Abstract] [Full Text] [Related]
8. von Willebrand disease family studies: comparison of three methods of analysis of the von Willebrand factor gene polymorphism related to a variable number tandem repeat sequence in intron 40.
Gaucher C; Mercier B; Mazurier C
Br J Haematol; 1992 Sep; 82(1):73-80. PubMed ID: 1419805
[TBL] [Abstract][Full Text] [Related]
9. Large deletions identified in patients with von Willebrand disease using multiple ligation-dependent probe amplification.
Yadegari H; Driesen J; Hass M; Budde U; Pavlova A; Oldenburg J
J Thromb Haemost; 2011 May; 9(5):1083-6. PubMed ID: 21410641
[No Abstract] [Full Text] [Related]
10. Expressed full-length von Willebrand factor containing missense mutations linked to type IIB von Willebrand disease shows enhanced binding to platelets.
Kroner PA; Kluessendorf ML; Scott JP; Montgomery RR
Blood; 1992 Apr; 79(8):2048-55. PubMed ID: 1373334
[TBL] [Abstract][Full Text] [Related]
11. Concentration of mRNA for von Willebrand factor in platelets of type I von Willebrand disease.
Takenaka T; Kuribayashi K; Tsukiyama M; Nakamine H; Fukuhara Y; Kuno T
Clin Chim Acta; 1996 Feb; 245(1):125-7. PubMed ID: 8646811
[No Abstract] [Full Text] [Related]
12. Re-evaluation of three Israeli families initially diagnosed with type 1 von Willebrand disease in light of the ISTH update on von Willebrand factor pathophysiology and classification.
Hashemi Soteh SM; Anson J; Inbal A; Peake IR; Goodeve AC
Haemophilia; 2008 May; 14(3):621-4. PubMed ID: 18384353
[No Abstract] [Full Text] [Related]
13. Instability of repeats of the von Willebrand factor gene variable number tandem repeat sequence in intron 40.
Eikenboom JC; Reitsma PH; van der Velden PA; Briët E
Br J Haematol; 1993 Jul; 84(3):533-5. PubMed ID: 8105872
[TBL] [Abstract][Full Text] [Related]
14. [Molecular genetic studies in the von Willebrand's syndrome].
Mannhalter C; Parzer S; Kyrle PA
Wien Klin Wochenschr; 1990 Sep; 102(17):491-6. PubMed ID: 1979896
[TBL] [Abstract][Full Text] [Related]
15. In-frame deletion of von Willebrand factor A domains in a dominant type of von Willebrand disease.
Bernardi F; Patracchini P; Gemmati D; Pinotti M; Schwienbacher C; Ballerini G; Marchetti G
Hum Mol Genet; 1993 May; 2(5):545-8. PubMed ID: 8518792
[TBL] [Abstract][Full Text] [Related]
16. Arg578Gln mutations in the von Willebrand factor gene in three unrelated cases of type IIB von Willebrand disease.
Piao YC; Lavergne JM; Boyer-Neumann C; Schandelong A; Alessi MC; Meyer D
Blood Coagul Fibrinolysis; 1993 Oct; 4(5):787-9. PubMed ID: 8292729
[TBL] [Abstract][Full Text] [Related]
17. The molecular biology of von Willebrand's disease.
Standen GR; Peake IR
Q J Med; 1991 May; 79(289):381-9. PubMed ID: 1681564
[No Abstract] [Full Text] [Related]
18. Germ-line mosaicism for a valine-to-methionine substitution at residue 553 in the glycoprotein Ib-binding domain of von Willebrand factor, causing type IIB von Willebrand disease.
Murray EW; Giles AR; Lillicrap D
Am J Hum Genet; 1992 Jan; 50(1):199-207. PubMed ID: 1729889
[TBL] [Abstract][Full Text] [Related]
19. [The application of molecular biology to thrombosis and hemostasis].
Niiya K; Ozawa T
Rinsho Byori; 1997 Apr; 45(4):305-9. PubMed ID: 9190431
[TBL] [Abstract][Full Text] [Related]
20. Cosegregation of von Willebrand factor gene polymorphisms and possible germinal mosaicism in type IIB von Willebrand disease.
Murray EW; Giles AR; Bridge PJ; Peake IR; Lillicrap DP
Blood; 1991 Apr; 77(7):1476-83. PubMed ID: 2009368
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]