Clinical and genetic heterogeneity of Seckel syndrome. (Q34528116)

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Language	Label	Description	Also known as
English	Clinical and genetic heterogeneity of Seckel syndrome.	scientific article

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scholarly article

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Europe PubMed Central

PubMed publication ID

12376940

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12376940%20AND%20SRC:MED&resulttype=core&format=json

retrieved

13 December 2019

title

Clinical and genetic heterogeneity of Seckel syndrome (English)

1 reference

stated in

Europe PubMed Central

PubMed publication ID

12376940

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12376940%20AND%20SRC:MED&resulttype=core&format=json

retrieved

13 December 2019

author

Stanislas Lyonnet

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3

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stated in

Europe PubMed Central

PubMed publication ID

12376940

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12376940%20AND%20SRC:MED&resulttype=core&format=json

retrieved

13 December 2019

Valérie Cormier-Daire

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10

1 reference

stated in

Europe PubMed Central

PubMed publication ID

12376940

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12376940%20AND%20SRC:MED&resulttype=core&format=json

retrieved

13 December 2019

Alain Verloes

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8

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Verloes A

1 reference

stated in

Europe PubMed Central

PubMed publication ID

12376940

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12376940%20AND%20SRC:MED&resulttype=core&format=json

retrieved

13 December 2019

author name string

Faivre L

series ordinal

1

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stated in

Europe PubMed Central

PubMed publication ID

12376940

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12376940%20AND%20SRC:MED&resulttype=core&format=json

retrieved

13 December 2019

Le Merrer M

series ordinal

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

12376940

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12376940%20AND%20SRC:MED&resulttype=core&format=json

retrieved

13 December 2019

Plauchu H

series ordinal

4

1 reference

stated in

Europe PubMed Central

PubMed publication ID

12376940

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12376940%20AND%20SRC:MED&resulttype=core&format=json

retrieved

13 December 2019

Dagoneau N

series ordinal

5

1 reference

stated in

Europe PubMed Central

PubMed publication ID

12376940

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12376940%20AND%20SRC:MED&resulttype=core&format=json

retrieved

13 December 2019

Campos-Xavier AB

series ordinal

6

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stated in

Europe PubMed Central

PubMed publication ID

12376940

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12376940%20AND%20SRC:MED&resulttype=core&format=json

retrieved

13 December 2019

Attia-Sobol J

series ordinal

7

1 reference

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Europe PubMed Central

PubMed publication ID

12376940

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12376940%20AND%20SRC:MED&resulttype=core&format=json

retrieved

13 December 2019

Munnich A

series ordinal

9

1 reference

stated in

Europe PubMed Central

PubMed publication ID

12376940

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12376940%20AND%20SRC:MED&resulttype=core&format=json

retrieved

13 December 2019

publication date

1 November 2002

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stated in

Europe PubMed Central

PubMed publication ID

12376940

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12376940%20AND%20SRC:MED&resulttype=core&format=json

retrieved

13 December 2019

published in

American Journal of Medical Genetics Part A

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stated in

Europe PubMed Central

PubMed publication ID

12376940

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12376940%20AND%20SRC:MED&resulttype=core&format=json

retrieved

13 December 2019

volume

112

1 reference

stated in

Europe PubMed Central

PubMed publication ID

12376940

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12376940%20AND%20SRC:MED&resulttype=core&format=json

retrieved

13 December 2019

issue

4

1 reference

stated in

Europe PubMed Central

PubMed publication ID

12376940

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12376940%20AND%20SRC:MED&resulttype=core&format=json

retrieved

13 December 2019

page(s)

379-383

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stated in

Europe PubMed Central

PubMed publication ID

12376940

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12376940%20AND%20SRC:MED&resulttype=core&format=json

retrieved

13 December 2019

cites work

SHOX mutations in dyschondrosteosis (Leri-Weill syndrome)

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2FAJMG.10677

retrieved

21 January 2018

A new locus for Seckel syndrome on chromosome 18p11.31-q11.2.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2FAJMG.10677

retrieved

21 January 2018

Do some patients with Seckel syndrome have hematological problems and/or chromosome breakage?

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2FAJMG.10677

retrieved

21 January 2018

A comprehensive genetic map of the human genome based on 5,264 microsatellites

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2FAJMG.10677

retrieved

21 January 2018

Autozygosity mapping of a seckel syndrome locus to chromosome 3q22. 1-q24.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2FAJMG.10677

retrieved

21 January 2018

Studies of microcephalic primordial dwarfism I: approach to a delineation of the Seckel syndrome

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2FAJMG.10677

retrieved

21 January 2018

Studies of microcephalic primordial dwarfism II: the osteodysplastic type II of primordial dwarfism

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2FAJMG.10677

retrieved

21 January 2018

Identifiers

DOI

10.1002/AJMG.10677

1 reference

stated in

Europe PubMed Central

PubMed publication ID

12376940

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12376940%20AND%20SRC:MED&resulttype=core&format=json

retrieved

13 December 2019

PubMed publication ID

12376940

1 reference

stated in

Europe PubMed Central

PubMed publication ID

12376940

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12376940%20AND%20SRC:MED&resulttype=core&format=json

retrieved

13 December 2019

ResearchGate publication ID

11083113

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