(Q51955269)

English

Severe lymphedema, intestinal lymphangiectasia, seizures and mild mental retardation: further case of Hennekam syndrome with a severe phenotype.

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scholarly article

1 reference

Europe PubMed Central

18 April 2018

http://europepmc.org/abstract/MED/12124738

Severe lymphedema, intestinal lymphangiectasia, seizures and mild mental retardation: further case of Hennekam syndrome with a severe phenotype. (English)

1 reference

Europe PubMed Central

18 April 2018

http://europepmc.org/abstract/MED/12124738

Hennekam syndrome

1 reference

based on heuristic

inferred from title

intestinal lymphangiectasis

1 reference

based on heuristic

inferred from title

author name string

Forzano F

1

1 reference

Europe PubMed Central

18 April 2018

http://europepmc.org/abstract/MED/12124738

Faravelli F

2

1 reference

Europe PubMed Central

18 April 2018

http://europepmc.org/abstract/MED/12124738

Loy A

3

1 reference

Europe PubMed Central

18 April 2018

http://europepmc.org/abstract/MED/12124738

Di Rocco M

4

1 reference

Europe PubMed Central

18 April 2018

http://europepmc.org/abstract/MED/12124738

publication date

1 July 2002

1 reference

Europe PubMed Central

18 April 2018

http://europepmc.org/abstract/MED/12124738

American Journal of Medical Genetics Part A

1 reference

Europe PubMed Central

18 April 2018

http://europepmc.org/abstract/MED/12124738

111

1 reference

Europe PubMed Central

18 April 2018

http://europepmc.org/abstract/MED/12124738

1

1 reference

Europe PubMed Central

18 April 2018

http://europepmc.org/abstract/MED/12124738

68-70

1 reference

Europe PubMed Central

18 April 2018

http://europepmc.org/abstract/MED/12124738

Expansion of the phenotype in Hennekam syndrome: a case with new manifestations.

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10509

21 January 2018

Craniosynostosis and kidney malformation in a case of Hennekam syndrome.

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10509

21 January 2018

Hennekam syndrome

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10509

21 January 2018

Mutations in FOXC2 (MFH-1), a forkhead family transcription factor, are responsible for the hereditary lymphedema-distichiasis syndrome

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10509

21 January 2018

Truncating mutations in FOXC2 cause multiple lymphedema syndromes

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10509

21 January 2018

Intestinal lymphangiectasia, lymphedema, mental retardation, and typical face: confirmation of the Hennekam syndrome.

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10509

21 January 2018

Autosomal recessive intestinal lymphangiectasia and lymphedema, with facial anomalies and mental retardation

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10509

21 January 2018

Missense mutations interfere with VEGFR-3 signalling in primary lymphoedema

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10509

21 January 2018

Lymphoscintigraphic manifestations of Hennekam syndrome--a case report.

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10509

21 January 2018

Identifiers

10.1002/AJMG.10509

1 reference

Europe PubMed Central

18 April 2018

http://europepmc.org/abstract/MED/12124738

1 reference

Europe PubMed Central

18 April 2018

http://europepmc.org/abstract/MED/12124738

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