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

Index « Auteurs » - entrée « Fiona Connell »
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Fiona Chapman < Fiona Connell < Fiona Cooke  Facettes :

List of bibliographic references

Number of relevant bibliographic references: 5.
Ident.Authors (with country if any)Title
000385 (2013) Kristiana Gordon [Royaume-Uni] ; Dörte Schulte ; Glen Brice ; Michael A. Simpson ; M Guy Roukens ; Andreas Van Impel ; Fiona Connell ; Kamini Kalidas ; Steve Jeffery ; Peter S. Mortimer ; Sahar Mansour ; Stefan Schulte-Merker ; Pia OstergaardMutation in vascular endothelial growth factor-C, a ligand for vascular endothelial growth factor receptor-3, is associated with autosomal dominant milroy-like primary lymphedema.
000725 (2010) Fiona Connell [Royaume-Uni] ; Kamini Kalidas ; Pia Ostergaard ; Glen Brice ; Tessa Homfray ; Lesley Roberts ; David J. Bunyan ; Sally Mitton ; Sahar Mansour ; Peter Mortimer (dermatologue)‎ [Royaume-Uni] ; Steve JefferyLinkage and sequence analysis indicate that CCBE1 is mutated in recessively inherited generalised lymphatic dysplasia.
000774 (2010) Sahar Mansour [Royaume-Uni] ; Fiona Connell [Royaume-Uni] ; Colin Steward [Royaume-Uni] ; Pia Ostergaard [Royaume-Uni] ; Glen Brice [Royaume-Uni] ; Sarah Smithson [Royaume-Uni] ; Peter Lunt [Royaume-Uni] ; Steve Jeffery [Royaume-Uni] ; Inderjeet Dokal [Royaume-Uni] ; Tom Vulliamy [Royaume-Uni] ; Brenda Gibson [Royaume-Uni] ; Shirley Hodgson [Royaume-Uni] ; Sally Cottrell [Royaume-Uni] ; Louise Kiely [Royaume-Uni] ; Lorna Tinworth [Royaume-Uni] ; Kamini Kalidas [Royaume-Uni] ; Ghulam Mufti [Royaume-Uni] ; Jackie Cornish [Royaume-Uni] ; Russell Keenan [Royaume-Uni] ; Peter Mortimer (dermatologue)‎ [Royaume-Uni] ; Victoria Murday [Royaume-Uni]Emberger syndrome—Primary lymphedema with myelodysplasia: Report of seven new cases
000934 (2008) Fiona Connell ; Glen Brice ; Peter Mortimer (dermatologue)‎ [Royaume-Uni]Phenotypic Characterization of Primary Lymphedema
000947 (2008) Fiona Connell [Royaume-Uni] ; Tessa Homfray [Royaume-Uni] ; Baskaran Thilaganathan [Royaume-Uni] ; Amarnath Bhide [Royaume-Uni] ; Iona Jeffrey [Royaume-Uni] ; Renata Hutt [Royaume-Uni] ; Peter Mortimer (dermatologue)‎ [Royaume-Uni] ; Sahar Mansour [Royaume-Uni]Congenital vascular malformations: A series of five prenatally diagnosed cases

List of associated KwdEn.i

Nombre de
documents
Descripteur
4Humans
4Lymphedema (genetics)
3Female
3Male
2Adolescent
2Adult
2Child
2Infant
2Lymphedema (pathology)
2Pedigree
2Phenotype
2Young Adult
1Abnormalities, Multiple
1Acute myelogenous leukemia
1Animals
1Base Sequence
1Calcium-Binding Proteins (genetics)
1Case study
1Child, Preschool
1Chromosome Mapping
1Chromosomes, Human, Pair 18 (genetics)
1Chromosomes, Human, Pair 7
1DNA Mutational Analysis (methods)
1DNA-Binding Proteins (genetics)
1Eyelashes (abnormalities)
1Family Health
1Fatal Outcome
1Fetal Death
1Frameshift Mutation (genetics)
1Genes, Recessive
1Genetic Linkage
1Genetic Predisposition to Disease (genetics)
1Genitalia (abnormalities)
1Genotype
1Infant, Newborn
1Leukemia, Myeloid, Acute (complications)
1Leukemia, Myeloid, Acute (genetics)
1Lower Extremity Deformities, Congenital
1Lymphedema
1Lymphedema (complications)
1Lymphedema (congenital)
1Monosomy
1Mutation
1Myelodysplastic Syndromes (complications)
1Myelodysplastic Syndromes (genetics)
1Myelodysplastic syndrome
1Polymorphism, Single Nucleotide
1Transcription Factors (genetics)
1Tumor Suppressor Proteins (genetics)
1Vascular Endothelial Growth Factor C (genetics)
1Vascular Endothelial Growth Factor Receptor-3 (genetics)
1Zebrafish

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