(Q51914961)

English

Complete trisomy 17p syndrome in a girl with der(14)t(14;17)(p11.2;p11.2).

scientific article published in August 2006

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scholarly article

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Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/16835929

Complete trisomy 17p syndrome in a girl with der(14)t(14;17)(p11.2;p11.2). (English)

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/16835929

1 reference

based on heuristic

inferred from title

Ludwine Messiaen

4

object named as

Ludwine Messiaen

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/16835929

author name string

Fady M Mikhail

1

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/16835929

Dawn McIlvried

2

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/16835929

R Lynn Holt

3

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/16835929

Maria D Descartes

5

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/16835929

Andrew J Carroll

6

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/16835929

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publication date

1 August 2006

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/16835929

American Journal of Medical Genetics

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Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/16835929

140

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/16835929

15

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/16835929

1647-1654

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/16835929

Trisomy 17p associated with Charcot-Marie-Tooth neuropathy type 1A phenotype: evidence for gene dosage as a mechanism in CMT1A

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.31330

21 January 2018

Identifiers

10.1002/AJMG.A.31330

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/16835929

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/16835929

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