(Q45861238)

17 December 2017

title

Exclusion of haemophilia B in male fetus by chorionic villus biopsy (English)

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17 December 2017

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T Tønnesen

1

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17 December 2017

F Søndergaard

2

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17 December 2017

F Güttler

3

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17 December 2017

I Oberlé

4

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17 December 2017

J P Moisan

5

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17 December 2017

J L Mandel

6

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17 December 2017

M Hauge

7

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17 December 2017

E M Damsgård

8

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17 December 2017

language of work or name

English

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publication date

1 October 1984

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17 December 2017

published in

The Lancet

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17 December 2017

volume

2

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17 December 2017

page(s)

932

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17 December 2017

issue

8408

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17 December 2017

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

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2884%2990690-1

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2884%2990690-1

7 January 2021

Close linkage of fragile X-mental retardation syndrome to haemophilia B and transmission through a normal male

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2884%2990690-1

7 January 2021

Prenatal Diagnosis of Sickle-Cell Anemia in the First Trimester of Pregnancy

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2884%2990690-1

7 January 2021

Differential nuclease sensitivity of the ovalbumin and β-globin chromatin regions in erythrocytes and oviduct cells of laying hen

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2884%2990690-1

7 January 2021

10.1016/S0140-6736(84)90690-1

Identifiers

DOI

1 reference

17 December 2017

PubMed ID

6148652

1 reference

17 December 2017