Genetic Techniques (trends) < Genetic Testing < Genetic Testing (economics)

Facettes : Author.f AffPays.f AffRegion.f AffVille.f AffOrg.f KwdFr.f Mesh.f MeshFr.f

List of bibliographic references indexed by Genetic Testing

Number of relevant bibliographic references: 10.

Ident.	Authors (with country if any)	Title
002253 (2015)	Kelly L. Jones [États-Unis] ; Ulrike Schwarze [États-Unis] ; Margaret P. Adam [États-Unis] ; Peter H. Byers [États-Unis] ; Heather C. Mefford [États-Unis]	A Homozygous B3GAT3 Mutation Causes a Severe Syndrome with Multiple Fractures, Extending the Number of Linkeropathy Syndromes
003025 (2013)	Jill M. Krapf [États-Unis] ; Andrew T. Goldstein	Two case presentations of profound labial edema as a presenting symptom of hypermobility-type Ehlers-Danlos syndrome.
004E82 (2011)	Robert J. Pignolo [États-Unis] ; Eileen M. Shore [États-Unis] ; Frederick S. Kaplan [États-Unis]	Fibrodysplasia Ossificans Progressiva: Clinical and Genetic Aspects
005247 (2011)	John S. Ferguson [Royaume-Uni] ; Shymalar Gunatheesan [Royaume-Uni] ; Glen Brice [Royaume-Uni] ; Rob Hastings [Royaume-Uni] ; Ruth Newbury-Ecob [Royaume-Uni] ; Peter S. Mortimer [Royaume-Uni] ; Sahar Mansour [Royaume-Uni]	Primary lymphedema with coarctation of the aorta: Possible new syndrome or variant of Irons–Bianchi syndrome?
006020 (2009)	Arash Ghalamkarpour [Belgique] ; Christian Debauche ; Eric Haan ; Nicole Van Regemorter ; Yves Sznajer ; Dominique Thomas ; Nicole Revencu ; Yves Gillerot ; Laurence M. Boon ; Miikka Vikkula	Sporadic in utero generalized edema caused by mutations in the lymphangiogenic genes VEGFR3 and FOXC2.
006599 (2009)	Smadar Eventov-Friedman [Israël] ; Amihood Singer [Israël] ; Eric S. Shinwell [Israël]	Microcephaly, lymphedema, chorioretinopathy and atrial septal defect: a case report and review of the literature
006B92 (2008)	Robert E. Ferrell [États-Unis] ; Mark A. Kimak ; Elizabeth C. Lawrence ; David N. Finegold	Candidate gene analysis in primary lymphedema.
008315 (2005)	M Y M. Ng ; T. Andrew ; T D Spector ; S. Jeffery	Linkage to the FOXC2 region of chromosome 16 for varicose veins in otherwise healthy, unselected sibling pairs
012A65 (????)	Betty Smoot ; Kord M. Kober ; Steven M. Paul ; Jon D. Levine ; Gary Abrams ; Judy Mastick ; Kimberly Topp ; Yvette P. Conley ; Christine A. Miaskowski	Potassium Channel Candidate Genes Predict the Development of Secondary Lymphedema Following Breast Cancer Surgery.
012E00 (????)	Glen Brice	Diagnostic difficulties in lymphedema distichiasis.

---

Pour manipuler ce document sous Unix (Dilib)

EXPLOR_STEP=$WICRI_ROOT/Wicri/Sante/explor/LymphedemaV1/Data/Main/Exploration

HfdIndexSelect -h $EXPLOR_AREA/Data/Main/Exploration/KwdEn.i -k "Genetic Testing" 

HfdIndexSelect -h $EXPLOR_AREA/Data/Main/Exploration/KwdEn.i  \
                -Sk "Genetic Testing" \
         | HfdSelect -Kh $EXPLOR_AREA/Data/Main/Exploration/biblio.hfd 

Pour mettre un lien sur cette page dans le réseau Wicri

{{Explor lien
   |wiki=    Wicri/Sante
   |area=    LymphedemaV1
   |flux=    Main
   |étape=   Exploration
   |type=    indexItem
   |index=    KwdEn.i
   |clé=    Genetic Testing
}}

---

This area was generated with Dilib version V0.6.31. Data generation: Sat Nov 4 17:40:35 2017. Site generation: Tue Feb 13 16:42:16 2024