(Q33787390)

29 July 2017

1 reference

title

Molecular diagnostic testing in Charcot-Marie-Tooth disease and related disorders. Approaches and results (English)

1 reference

Christine Van Broeckhoven

29 July 2017

6

object named as

Van Broeckhoven C

1 reference

29 July 2017

De Jonghe P

1

1 reference

29 July 2017

Nelis E

2

1 reference

29 July 2017

Timmerman V

3

1 reference

29 July 2017

Löfgren A

4

1 reference

29 July 2017

Martin JJ

5

1 reference

29 July 2017

language of work or name

English

0 references

publication date

1 September 1999

1 reference

Annals of the New York Academy of Sciences

29 July 2017

1 reference

29 July 2017

883

1 reference

29 July 2017

389-396

1 reference

De-novo mutation in hereditary motor and sensory neuropathy type I.

29 July 2017

1 reference

Crossref

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1999.TB08600.X

Hereditary neuropathy with liability to pressure palsies. Phenotypic differences between patients with the common deletion and a PMP22 frame shift mutation.

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1999.TB08600.X

Pregnancy after preimplantation genetic diagnosis for Charcot-Marie-Tooth disease type 1A.

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1999.TB08600.X

10.1111/J.1749-6632.1999.TB08600.X

21 January 2018

Identifiers

DOI

1 reference

release_juvjtjqdavaghaxws54qo347ne

29 July 2017

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/juvjtjqdavaghaxws54qo347ne

mapped directly with Wikidata item

24 November 2022

based on heuristic

1 reference