(Q41187736)

28 September 2017

Somatic origin of inherited haemophilia A. (English)

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28 September 2017

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A H Bröcker-Vriends

1

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28 September 2017

E Briët

2

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28 September 2017

J C Dreesen

3

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28 September 2017

B Bakker

4

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28 September 2017

P Reitsma

5

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28 September 2017

H Pannekoek

6

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28 September 2017

J J van de Kamp

7

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28 September 2017

P L Pearson

8

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28 September 2017

1 August 1990

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28 September 2017

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28 September 2017

85

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28 September 2017

288-292

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28 September 2017

3

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https://scigraph.springernature.com/pub.10.1007/bf00206748

28 September 2017

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cites work

Review and hypotheses: somatic mosaicism: observations related to clinical genetics

1 reference

12 December 2020

Genotype assignment of haemophilia A by use of intragenic and extragenic restriction fragment length polymorphisms

1 reference

12 December 2020

Half chromatid mutations: transmission in humans?

1 reference

12 December 2020

Genetic studies of germinal mosaicism in Drosophila melanogaster using the mutable wc gene

1 reference

12 December 2020

Germinal mosaicism increases the recurrence risk for 'new' Duchenne muscular dystrophy mutations

1 reference

12 December 2020

Inhibition of human coagulation factor VIII by monoclonal antibodies. Mapping of functional epitopes with the use of recombinant factor VIII fragments

1 reference

12 December 2020

Recurrent de novo interstitial deletion of 16q in two mentally retarded sisters.

1 reference

12 December 2020

Mosaicism and sporadic haemophilia: implications for carrier determination

1 reference

12 December 2020

Maternal duplication associated with gene deletion in sporadic hemophilia

1 reference

12 December 2020

Mosaicism for an intragenic deletion in a boy with mild ornithine transcarbamylase deficiency

1 reference

12 December 2020

Quantitative estimation of proteins by electrophoresis in agarose gel containing antibodies

1 reference

12 December 2020

The prezygotic origin of structural mosaicisms

1 reference

12 December 2020

Genetic mapping and diagnosis of haemophilia A achieved through a BclI polymorphism in the factor VIII gene

1 reference

12 December 2020

The genetics of Rett syndrome: the consequences of a disorder where every case is a new mutation.

1 reference

12 December 2020

A partial deletion of the muscular dystrophy gene transmitted twice by an unaffected male.

1 reference

12 December 2020

Characterization of the human factor VIII gene.

1 reference

12 December 2020

Recurrence risk in de novo 21q21q translocation Down syndrome

1 reference

12 December 2020

Germinal mosaicism in achondroplasia: a family with 3 affected siblings of normal parents

1 reference

12 December 2020

Genetic Analysis of Seven Newly Discovered Mutant Alleles at Locus T in the House Mouse

1 reference

12 December 2020

Detection of the carrier state in hereditary coagulation disorders. I

1 reference

12 December 2020

A somatic mosaic for haemophilia A detected at the DNA level.

1 reference

12 December 2020

Recurrence risks for germinal mosaics

1 reference

12 December 2020

Molecular genetics of hemophilia A in man (factor VIII deficiency).

1 reference

12 December 2020

Carrier detection in hemophilia A: a cooperative international study. II. The efficacy of a universal discriminant.

1 reference

12 December 2020

Gonadal mosaicism in pseudoachondroplasia.

1 reference

12 December 2020

Gonadal mosaicism and genetic counseling for X-linked recessive lethals

1 reference

12 December 2020

Genetic screening for hemophilia A (classic hemophilia) with a polymorphic DNA probe

1 reference

12 December 2020

Germline mosaicism and Duchenne muscular dystrophy mutations

1 reference

12 December 2020

Recurrence rate for de novo 21q21q translocation Down syndrome: A study of 112 families

1 reference

12 December 2020

Unusual scarcity of restriction site polymorphism in the human thyroglobulin gene. A linkage study suggesting autosomal dominance of a defective thyroglobulin allele

1 reference

12 December 2020

Isolation of probes detecting restriction fragment length polymorphisms from X chromosome-specific libraries: potential use for diagnosis of Duchenne muscular dystrophy

1 reference

12 December 2020

Germinal mosaicism in Apert syndrome

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00206748

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Dimensions Publication ID

28 September 2017

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1 reference