(Q35562055)

8 August 2017

1 reference

title

Further delineation of Hennekam syndrome (English)

1 reference

8 August 2017

L. I. Al-Gazali

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A14564208

22 March 2024

J. Hertecant

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A14564208

22 March 2024

R. Ahmed

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A14564208

22 March 2024

N. A. Khan

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A14564208

22 March 2024

R. Padmanabhan

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A14564208

22 March 2024

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=14564208

22 March 2024

publication date

1 October 2003

1 reference

full work available at URL

8 August 2017

http://journals.lww.com/00019605-200310000-00003

1 reference

https://api.crossref.org/works/10.1097/00019605-200310000-00003

22 March 2024

published in

Clinical Dysmorphology

1 reference

8 August 2017

12

1 reference

8 August 2017

4

1 reference

8 August 2017

227-232

1 reference

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

8 August 2017

1

1 reference

https://api.crossref.org/works/10.1097/00019605-200310000-00003

Craniosynostosis and kidney malformation in a case of Hennekam syndrome.

22 March 2024

2

1 reference

https://api.crossref.org/works/10.1097/00019605-200310000-00003

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

22 March 2024

3

1 reference

https://api.crossref.org/works/10.1097/00019605-200310000-00003

Prox1 is a master control gene in the program specifying lymphatic endothelial cell fate

22 March 2024

5

1 reference

https://api.crossref.org/works/10.1097/00019605-200310000-00003

Two brothers with Hennekam syndrome and cerebral abnormalities.

22 March 2024

6

1 reference

https://api.crossref.org/works/10.1097/00019605-200310000-00003

Lymphoscintigraphic manifestations of Hennekam syndrome--a case report.

22 March 2024

8

1 reference

https://api.crossref.org/works/10.1097/00019605-200310000-00003

Early death in two sisters with Hennekam syndrome

22 March 2024

9

1 reference

https://api.crossref.org/works/10.1097/00019605-200310000-00003

End-stage renal disease in a patient with congenital lymphangiectasia and lymphedema

22 March 2024

10

1 reference

https://api.crossref.org/works/10.1097/00019605-200310000-00003

Lymphedema-lymphangiectasia-mental retardation (Hennekam) syndrome: a review

22 March 2024

11

1 reference

https://api.crossref.org/works/10.1097/00019605-200310000-00003

Prox1 function is required for the development of the murine lymphatic system

22 March 2024

12

1 reference

https://api.crossref.org/works/10.1097/00019605-200310000-00003

22 March 2024

Identifiers

1 reference

8 August 2017

1 reference