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

Index « Auteurs » - entrée « V. A. Murday »
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V. A. Hill < V. A. Murday < V. A. Varney  Facettes :

List of bibliographic references

Number of relevant bibliographic references: 3.
Ident.Authors (with country if any)Title
000E42 (2001) S. Mansour [Royaume-Uni] ; H. Woffendin [Royaume-Uni] ; S. Mitton [Royaume-Uni] ; I. Jeffery [Royaume-Uni] ; T. Jakins [Royaume-Uni] ; S. Kenwrick [Royaume-Uni] ; V. A. Murday [Royaume-Uni]Incontinentia pigmenti in a surviving male is accompanied by hypohidrotic ectodermal dysplasia and recurrent infection
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
001031 (1999) J. Mangion [Royaume-Uni] ; N. Rahman [Royaume-Uni] ; S. Mansour [Royaume-Uni] ; G. Brice [Royaume-Uni] ; J. Rosbotham [Royaume-Uni] ; A. H. Child [Royaume-Uni] ; V. A. Murday [Royaume-Uni] ; Peter Mortimer (dermatologue)‎ [Royaume-Uni] ; R. Barfoot [Royaume-Uni] ; A. Sigurdsson [Royaume-Uni] ; S. Edkins [Royaume-Uni] ; M. Sarfarazi ; K. Burnand [Royaume-Uni] ; A. L. Evans [Royaume-Uni] ; T. O. Nunan [Royaume-Uni] ; M. R. Stratton [Royaume-Uni] ; S. Jeffery [Royaume-Uni]A Gene for Lymphedema-Distichiasis Maps to 16q24.3

List of associated KwdEn.i

Nombre de
documents		Descripteur
3Family study
3Female
3Human
3Humans
3Lymphedema
3Male
2Distichiasis
2Genetic determinism
2Lymphedema (genetics)
2Mutation
2Pedigree
2Phenotype
1Anhidrotic ectodermal dysplasia
1Bullous dermatosis
1Case study
1Chromosome 16
1Chromosome E16
1Chromosomes, Human, Pair 16 (genetics)
1Codon, Terminator
1Concomitant disease
1DNA (chemistry)
1DNA (genetics)
1DNA Mutational Analysis
1DNA-Binding Proteins (genetics)
1Deletion
1Ectodermal Dysplasia (complications)
1Ectodermal Dysplasia (genetics)
1Ectodermal Dysplasia (physiopathology)
1Eyelid Diseases (genetics)
1Eyelid Diseases (pathology)
1Family Health
1Forkhead Transcription Factors
1Gene
1Genetic Linkage (genetics)
1Genetic Markers (genetics)
1Genetic mapping
1Genome
1Hair
1Hematologic Diseases (complications)
1Hemopathy
1Hypohidrosis (complications)
1Hypohidrosis (genetics)
1Hypohidrosis (physiopathology)
1I-kappa B Kinase
1Immune deficiency
1Incontinentia Pigmenti (complications)
1Incontinentia Pigmenti (genetics)
1Incontinentia Pigmenti (physiopathology)
1Incontinentia pigmenti
1Infant, Newborn
1Infection
1Infection (etiology)
1Insertion
1Intestinal Absorption
1Linkage
1Locus
1Long arm
1Lower limb
1Lymphedema (complications)
1Lymphedema (diagnosis)
1Lymphedema (pathology)
1Lymphedema-distichiasis
1Molecular Sequence Data
1Mutagenesis, Insertional
1Osteosclerosis
1Pathogenesis
1Physical Chromosome Mapping
1Protein-Serine-Threonine Kinases (genetics)
1Recurrence
1Recurrent
1Sequence Deletion
1Survival
1Survivors
1Symptomatology
1Transcription Factors (genetics)
1Transcription factor
1Transcription factor NFκB
1X Chromosome

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