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Analysis
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Serveur d'exploration sur le lymphœdème - Analysis (UK)

Index « Auteurs » - entrée « R. Bell »
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R. Beard < R. Bell < R. Best  Facettes :

List of bibliographic references

Number of relevant bibliographic references: 5.
Ident.Authors (with country if any)Title
000B59 (2005) G. Brice [Royaume-Uni] ; A H Child [Royaume-Uni] ; A. Evans [Royaume-Uni] ; R. Bell [Royaume-Uni] ; S. Mansour [Royaume-Uni] ; K. Burnand [Royaume-Uni] ; M. Sarfarazi [États-Unis] ; S. Jeffery [Royaume-Uni] ; Peter Mortimer (dermatologue)‎ [Royaume-Uni]Milroy disease and the VEGFR-3 mutation phenotype
000C91 (2003) A L Evans [Royaume-Uni] ; R. Bell ; G. Brice [Royaume-Uni] ; P. Comeglio [Royaume-Uni] ; C. Lipede ; S. Jeffery ; Peter Mortimer (dermatologue)‎ [Royaume-Uni] ; M. Sarfarazi [États-Unis] ; A H Child [Royaume-Uni]Identification of eight novel VEGFR-3 mutations in families with primary congenital lymphoedema
000D65 (2002) G. Brice [Royaume-Uni] ; S. Mansour [Royaume-Uni] ; R. Bell [Royaume-Uni] ; J R O. Collin [Royaume-Uni] ; A H Child [Royaume-Uni] ; A F Brady [Royaume-Uni] ; M. Sarfarazi [États-Unis] ; K G Burnand [Royaume-Uni] ; S. Jeffery [Royaume-Uni] ; Peter Mortimer (dermatologue)‎ [Royaume-Uni] ; V A Murday [Royaume-Uni]Analysis of the phenotypic abnormalities in lymphoedema-distichiasis syndrome in 74 patients with FOXC2 mutations or linkage to 16q24
000E70 (2001) R. Bell [Royaume-Uni] ; G. Brice [Royaume-Uni] ; A. H. Child [Royaume-Uni] ; V. A. Murday [Royaume-Uni] ; S. Mansour [Royaume-Uni] ; C. J. Sandy [Royaume-Uni] ; J. R. O. Collin [Royaume-Uni] ; A. F. Brady [Royaume-Uni] ; D. F. Callen [Australie] ; K. Burnand [Royaume-Uni] ; Peter Mortimer (dermatologue)‎ [Royaume-Uni] ; S. Jeffery [Royaume-Uni]Analysis of lymphoedema-distichiasis families for FOXC2 mutations reveals small insertions and deletions throughout the gene
000F09 (2000) R. Bell ; G. Brice ; A H Child ; V A Murday ; S. Mansour ; C J Sandy ; J R O. Collin ; Peter Mortimer (dermatologue)‎ [Royaume-Uni] ; D F Callen ; K. Burnand ; S. JefferyReduction of the genetic interval for lymphoedema-distichiasis to below 2 Mb

List of associated KwdEn.i

Nombre de
documents		Descripteur
5Female
5Humans
5Lymphedema (genetics)
5Male
4Mutation
3DNA (genetics)
3Family Health
3Family study
3Lymphedema
3Pedigree
3Phenotype
2Adult
2Chromosomes, Human, Pair 16 (genetics)
2DNA (chemistry)
2DNA Mutational Analysis
2DNA-Binding Proteins (genetics)
2Distichiasis
2Eyelashes (abnormalities)
2Eyelid Diseases (genetics)
2Eyelid Diseases (pathology)
2Forkhead Transcription Factors
2Haplotypes
2Human
2Lymphedema (pathology)
2Sequence Deletion
2Transcription Factors (genetics)
2VEGFR-3
2Vascular Endothelial Growth Factor Receptor-3 (genetics)
1Abnormalities, Multiple (diagnostic imaging)
1Abnormalities, Multiple (genetics)
1Adolescent
1Age of Onset
1Child
1Child, Preschool
1Chromosome E16
1Congenital
1Deletion
1Eyelashes (diagnostic imaging)
1FOXC2
1Gene
1Genetic Linkage (genetics)
1Genetic determinism
1Genotype
1Heterozygote Detection
1Identification
1Infant
1Insertion
1Linkage
1Lymphedema (congenital)
1Lymphedema (diagnosis)
1Lymphedema (diagnostic imaging)
1Lymphedema (epidemiology)
1Lymphography (methods)
1Microsatellite Repeats
1Milroy disease
1Mutagenesis, Insertional
1Mutation, Missense
1Nails, Malformed
1Papilloma (pathology)
1Pathogenesis
1Puberty (genetics)
1Radionuclide Imaging
1Saphenous Vein (pathology)
1Syndrome
1Transcription factor
1Urogenital Abnormalities (diagnosis)
1VEGFR-3, vascular endothelial growth factor receptor 3
1Varicose Veins (diagnosis)
1distichiasis
1hydrocoele
1lymphoedema
1primary congenital lymphoedema
1primary lymphoedema
1varicose veins

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EXPLOR_STEP=$WICRI_ROOT/Wicri/Sante/explor/LymphedemaV1/Data/UK/Analysis

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HfdIndexSelect -h $EXPLOR_AREA/Data/UK/Analysis/Author.i  \
                -Sk "R. Bell" \
         | HfdSelect -Kh $EXPLOR_AREA/Data/UK/Analysis/biblio.hfd

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