(Q72675759)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7909449%20AND%20SRC:MED&resulttype=core&format=json

28 October 2019

title

Seeming homozygosity in type-IIB von Willebrand's disease due to a polymorphism within the sequence of a commonly used primer (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7909449%20AND%20SRC:MED&resulttype=core&format=json

28 October 2019

main subject

von Willebrand's disease

1 reference

1 reference

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7909449%20AND%20SRC:MED&resulttype=core&format=json

28 October 2019

author name string

P H Reitsma

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7909449%20AND%20SRC:MED&resulttype=core&format=json

28 October 2019

E Briët

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7909449%20AND%20SRC:MED&resulttype=core&format=json

28 October 2019

publication date

1 March 1994

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7909449%20AND%20SRC:MED&resulttype=core&format=json

28 October 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7909449%20AND%20SRC:MED&resulttype=core&format=json

28 October 2019

volume

68

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7909449%20AND%20SRC:MED&resulttype=core&format=json

28 October 2019

issue

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7909449%20AND%20SRC:MED&resulttype=core&format=json

28 October 2019

page(s)

139-141

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7909449%20AND%20SRC:MED&resulttype=core&format=json

von Willebrand disease: a database of point mutations, insertions, and deletions. For the Consortium on von Willebrand Factor Mutations and Polymorphisms, and the Subcommittee on von Willebrand Factor of the Scientific and Standardization Committee

28 October 2019

cites work

1 reference

12 December 2020

Mutations in severe, type III von Willebrand's disease in the Dutch population: candidate missense and nonsense mutations associated with reduced levels of von Willebrand factor messenger RNA

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12 December 2020

von Willebrand factor and von Willebrand disease

1 reference

12 December 2020

Human von Willebrand factor gene and pseudogene: structural analysis and differentiation by polymerase chain reaction

1 reference

12 December 2020

Structure of the gene for human von Willebrand factor

1 reference

12 December 2020

Trinucleotide repeat polymorphism at the human intestinal fatty acid binding protein gene (FABP2)

1 reference

12 December 2020

Dinucleotide repeat polymorphism at the D4S174 locus

1 reference

12 December 2020

Molecular basis of von Willebrand disease type IIB. Candidate mutations cluster in one disulfide loop between proposed platelet glycoprotein Ib binding sequences

1 reference

12 December 2020

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

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF01727418

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7909449%20AND%20SRC:MED&resulttype=core&format=json

28 October 2019

1 reference