marfanoid Pages on BioPortfolio:

BioPortfolio - marfanoid
The Lujan-Fryns syndrome or X-linked mental retardation with marfanoid habitus syndrome is a ... Perrault syndrome with Marfanoid habitus in two siblings. ...
http://www.bioportfolio.com/search/marfanoid.html...

BioPortfolio - ZDHHC9
Mutations in ZDHHC9 have also been reported in XLMR with marfanoid habitus and in one .... Mutations in ZDHHC9, a palmitoyltransferase of NRAS and HRAS, . ...
http://www.bioportfolio.com/search/ZDHHC9.html...

BioPortfolio - Cutis Laxa
CLK4 CDC-like kinase 4 · CLM cutis laxa with marfanoid phenotype · CLMN calmin ( calponin-like, ... http://www.bioportfolio.com/search/marfanoid.html. ...
http://www.bioportfolio.com/search/Cutis_Laxa.html...

BioPortfolio - wandering spleen
Wandering Spleen - BioPortfolio - Indepth. ... Marfanoid hypermobility syndrome and skeletal abnormalities in a rare case of torsion of wandering spleen. ...
http://www.bioportfolio.com/search/wandering_spleen.html...

BioPortfolio - ectopia lentis
The roles of two novel FBN1 gene mutations in the genotype-phenotype correlations of Marfan syndrome and ectopia lentis patients with marfanoid
habitus. ...
http://www.bioportfolio.com/search/ectopia_lentis.html...

BioPortfolio - CBLC
Marfanoid features in a child with combined methylmalonic aciduria and homocystinuria (CblC type). ... http://www.bioportfolio.com/search/marfanoid.
html. ...
http://www.bioportfolio.com/search/CBLC.html...

BioPortfolio - Shprintzen
Shprintzen-Goldberg syndrome is one of a group of disorders characterized by craniosynostosis and marfanoid habitus. Eleven cases were reported previously.
...
http://www.bioportfolio.com/search/Shprintzen.html...

BioPortfolio - CUTIS LAXA
BioPortfolio "cutis laxa with marfanoid phenotype" Antibody Antibody Search Find antibodies and immune reagents from over 200 suppliers. ...
http://www.bioportfolio.com/search/CUTIS_LAXA.html...

BioPortfolio - Arachnodactyly research
Perrault syndrome with Marfanoid habitus in two siblings. ... Marfanoid features in a child with combined methylmalonic aciduria and homocystinuria (CblC ...
http://www.bioportfolio.com/indepth/Arachnodactyly/research....

Results from other life science and pharmaceutical sites:

Mental retardation with marfanoid syndrome: presen...[Brain Dev ...
X-linked mental retardation with marfanoid habitus. [Am J Med Genet. 1987]; A form of X-linked mental retardation with marfanoid habitus. [Am J Med Genet. ...
http://www.ncbi.nlm.nih.gov/pubmed/8250152...

Mutation in fibrillin-1 and the Marfanoid-craniosynostosis ...
Mutation in fibrillin-1 and the Marfanoid-craniosynostosis (Shprintzen-Goldberg) syndrome. Sumesh Sood1, Zayz A. Eldadah1, Wilma L. Krause2, Iain Mclntosh1, ...
http://www.nature.com/ng/journal/v12/n2/abs/ng0296-209.html...

Lujan-Fryns syndrome (mental retardation, X-linked, marfanoid habitus)
The Lujan-Fryns syndrome or X-linked mental retardation with marfanoid habitus syndrome is a syndromal X-linked form of mental retardation, ...
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=15...

Marfanoid Habitus, Dysmorphic Features, and Web Neck
Bilateral pneumothoraces and aortic dilatation developed in a 25-year-old white man with marfanoid habitus, dysmorphic features, web neck, and intellectual ...
http://www.medscape.com/viewarticle/410686...

Marfanoid hypermobility syndrome associated with coarctation of ...
The condition is labelled as Marfanoid hypermobility syndrome. In the patient described here, the Marfanoid hypermobility syndrome was associated with ...
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=48...

Marfanoid Habitus, Dysmorphic Features, and Web Neck
Marfan syndrome, SGS, LFS, and CCA are all associated with marfanoid habitus, yet individually they can usually be separated by characteristic clinical ...
http://www.medscape.com/viewarticle/410686_3...

Marfanoid features in a child with combined methyl...[J Inherit ...
The girl presented at the age of 13 years with macrocytic anaemia, cognitive regression and Marfanoid features such as increased arm-span, arachnodactyly,
...
http://www.ncbi.nlm.nih.gov/pubmed/17768669...

Unusual complications in siblings with marfanoid phenotype.
Visceral diverticula have been described only once in four adults with marfanoid features of recessive inheritance. Two siblings of a consanguineous ...
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=15...

X-linked mental retardation with marfanoid habitus. [Am J Med ...
[Chromosome X-linked mental retardation and marfanoid syndrome] [J Genet Hum. ... 1991]; Mental retardation with marfanoid syndrome: presentation of a ...
http://www.ncbi.nlm.nih.gov/pubmed/3322000...

BioMed Central | Full text | Necrotic gangrenous intrathoracic ...
In this case report, we aim to demonstrate a congenital diaphragmatic hernia in an adult marfanoid patient which required emergency treatment ...
http://www.biomedcentral.com/1471-2482/5/4...

Home Marketing Services News Reports Company Profiles InDepth Drug Discovery Careers Conferences Videos Search Contact
	Nothing in this website should be used in place of personal medical advice from your own qualified medical practitioner. See User Agreement Send comments and feedback to: Peter Barfoot Managing Director, BioPortfolio Ltd. UK Tel: (+44) 1300 321501 USA Voicemail and Fax: (+1) 415 680 2472	All rights reserved. All other trademarks recognized. BioPortfolio Limited is registered in England & Wales at Wessex Barn, Dorchester Road, Frampton, Dorset, DT2 9NB, UK. No.3312883 VAT No. GB 744 6483 10 Copyright 1997-2008 - BioPortfolio Limited.