(Q51937296)

English

Classical West "syndrome" phenotype with a subtelomeric 4p trisomy.

scientific article published in October 2004

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/15378535

Classical West "syndrome" phenotype with a subtelomeric 4p trisomy. (English)

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/15378535

2

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/15378535

13

object named as

A Verloes

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/15378535

author name string

Marion Gérard-Blanluet

1

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/15378535

C Munier

3

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/15378535

M Le Lorc'h

4

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/15378535

S Kanafani

5

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/15378535

M Sinico

6

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/15378535

C Touboul

7

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Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/15378535

J M Levaillant

8

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/15378535

B Haddad

9

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Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/15378535

N Lopez

10

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/15378535

F Lelong

11

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/15378535

T Billette De Villemeur

12

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/15378535

E Borghi

14

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Europe PubMed Central

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17 April 2018

http://europepmc.org/abstract/MED/15378535

language of work or name

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publication date

1 October 2004

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Europe PubMed Central

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17 April 2018

http://europepmc.org/abstract/MED/15378535

American Journal of Medical Genetics

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PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/15378535

130A

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17 April 2018

http://europepmc.org/abstract/MED/15378535

3

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17 April 2018

http://europepmc.org/abstract/MED/15378535

299-302

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Europe PubMed Central

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17 April 2018

http://europepmc.org/abstract/MED/15378535

Disruption of the serine/threonine kinase 9 gene causes severe X-linked infantile spasms and mental retardation

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.30314

21 January 2018

Perfect endings: a review of subtelomeric probes and their use in clinical diagnosis

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.30314

21 January 2018

Interstitial deletion of chromosome 7q in a patient with Williams syndrome and infantile spasms.

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.30314

21 January 2018

WHSC1, a 90 kb SET domain-containing gene, expressed in early development and homologous to a Drosophila dysmorphy gene maps in the Wolf-Hirschhorn syndrome critical region and is fused to IgH in t(4;14) multiple myeloma

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.30314

21 January 2018

ON A PECULIAR FORM OF INFANTILE CONVULSIONS,

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.30314

21 January 2018

Identifiers

10.1002/AJMG.A.30314

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/15378535

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/15378535

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