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

Index « Auteurs » - entrée « A H Child »
Attention, ce site est en cours de développement !
Attention, site généré par des moyens informatiques à partir de corpus bruts.
Les informations ne sont donc pas validées.
A G Diamond < A H Child < A H Crosby  Facettes :

List of bibliographic references

Number of relevant bibliographic references: 4.
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
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
4Female
4Humans
4Lymphedema (genetics)
4Male
3Mutation
3Phenotype
2Adult
2Chromosomes, Human, Pair 16 (genetics)
2DNA (genetics)
2Eyelashes (abnormalities)
2Family Health
2Family study
2Haplotypes
2Lymphedema
2Pedigree
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
1DNA (chemistry)
1DNA Mutational Analysis
1DNA-Binding Proteins (genetics)
1Distichiasis
1Eyelashes (diagnostic imaging)
1Eyelid Diseases (genetics)
1Eyelid Diseases (pathology)
1FOXC2
1Forkhead Transcription Factors
1Gene
1Genetic Linkage (genetics)
1Genetic determinism
1Genotype
1Heterozygote Detection
1Human
1Identification
1Infant
1Linkage
1Lymphedema (congenital)
1Lymphedema (diagnosis)
1Lymphedema (diagnostic imaging)
1Lymphedema (epidemiology)
1Lymphedema (pathology)
1Lymphography (methods)
1Microsatellite Repeats
1Milroy disease
1Mutation, Missense
1Nails, Malformed
1Papilloma (pathology)
1Pathogenesis
1Puberty (genetics)
1Radionuclide Imaging
1Saphenous Vein (pathology)
1Sequence Deletion
1Syndrome
1Transcription Factors (genetics)
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

HfdIndexSelect -h $EXPLOR_AREA/Data/UK/Analysis/Author.i -k "A H Child" 

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

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   |index=    Author.i
   |clé=    A H Child
}}
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