Application of three intragenic DNA polymorphisms for carrier detection in haemophilia B. - Wikidata - wikimedia - TriplyDB

Application of three intragenic DNA polymorphisms for carrier detection in haemophilia B.

Application of three intragenic DNA polymorphisms for carrier detection in haemophilia B.

http://www.wikidata.org/entity/Q33673323

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Linkage analysis using multiple Xq DNA polymorphisms in normal families, families with the fragile X syndrome, and other families with X linked conditions.

P2860

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P2860

Application of three intragenic DNA polymorphisms for carrier detection in haemophilia B.

http://www.wikidata.org/entity/Q33673323

description

1986 nî lūn-bûn

@nan

1986 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

@hyw

1986 թվականի օգոստոսին հրատարակված գիտական հոդված

@hy

1986年の論文

@ja

1986年論文

@yue

1986年論文

@zh-hant

1986年論文

@zh-hk

1986年論文

@zh-mo

1986年論文

@zh-tw

1986年论文

@wuu

name

Application of three intragenic DNA polymorphisms for carrier detection in haemophilia B.

@ast

Application of three intragenic DNA polymorphisms for carrier detection in haemophilia B.

@en

type

label

Application of three intragenic DNA polymorphisms for carrier detection in haemophilia B.

@ast

Application of three intragenic DNA polymorphisms for carrier detection in haemophilia B.

@en

prefLabel

Application of three intragenic DNA polymorphisms for carrier detection in haemophilia B.

@ast

Application of three intragenic DNA polymorphisms for carrier detection in haemophilia B.

@en

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P1433

Journal of Medical Genetics

P1476

Application of three intragenic DNA polymorphisms for carrier detection in haemophilia B.

@en

P2093

Connor JM

http://www.w3.org/2001/XMLSchema#string

Forbes CD

http://www.w3.org/2001/XMLSchema#string

Hann IM

http://www.w3.org/2001/XMLSchema#string

Lowe GD

http://www.w3.org/2001/XMLSchema#string

Pettigrew AF

http://www.w3.org/2001/XMLSchema#string

Shiach C

http://www.w3.org/2001/XMLSchema#string

P2860

Application of an intragenic genomic probe to genetic counselling for haemophilia B in the west of Scotland

Carrier detection of Hemophilia B by using a restriction site polymorphism associated with the coagulation Factor IX gene

Carrier detection in haemophilia B using two further intragenic restriction fragment length polymorphisms.

Identification of the molecular defect in factor IX Chapel Hill: substitution of histidine for arginine at position 145.

Polymorphism of DNA sequence adjacent to human beta-globin structural gene: relationship to sickle mutation

Population genetics of C4 with the use of complementary DNA probes.

Gene deletion in an Italian haemophilia B subject.

Characterisation and use of an intragenic polymorphic marker for detection of carriers of haemophilia B (factor IX deficiency).

Gene deletions in patients with haemophilia B and anti-factor IX antibodies.

Antenatal diagnosis and carrier detection of haemophilia A using factor VIII gene probe.

P304

300-309

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scholarly article

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P433

4

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P478

23

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P577

1986-08-01T00:00:00Z

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P698

3018248

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P921

P932

1049694

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