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

Index « Auteurs » - entrée « Ps Mortimer »
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Prosper P. Chaki < Ps Mortimer < Pt Khaw  Facettes :

List of bibliographic references

Number of relevant bibliographic references: 3.
Ident.Authors (with country if any)Title
000440 (2013) Fc Connell [Royaume-Uni] ; K. Gordon [Royaume-Uni] ; G. Brice [Royaume-Uni] ; V. Keeley [Royaume-Uni] ; S. Jeffery [Royaume-Uni] ; Ps Mortimer [Royaume-Uni] ; S. Mansour [Royaume-Uni] ; P. Ostergaard [Royaume-Uni]The classification and diagnostic algorithm for primary lymphatic dysplasia: an update from 2010 to include molecular findings
000477 (2013) G. Brice [Royaume-Uni] ; P. Ostergaard ; S. Jeffery ; K. Gordon [Royaume-Uni] ; Ps Mortimer [Royaume-Uni] ; S. MansourA novel mutation in GJA1 causing oculodentodigital syndrome and primary lymphoedema in a three generation family
000582 (2012) Fc Connell [Royaume-Uni] ; K. Kalidas ; P. Ostergaard ; G. Brice [Royaume-Uni] ; V. Murday [Royaume-Uni] ; Ps Mortimer ; I. Jeffrey [Royaume-Uni] ; S. Jeffery ; Sahar Mansour [Royaume-Uni]CCBE1 mutations can cause a mild, atypical form of generalized lymphatic dysplasia but are not a common cause of non‐immune hydrops fetalis

List of associated KwdEn.i

Nombre de
documents
Descripteur
3Humans
3Lymphedema (diagnosis)
2Craniofacial Abnormalities (diagnosis)
2Craniofacial Abnormalities (genetics)
2Female
2Lymphedema (genetics)
2Mutation
1Abnormalities, Multiple (genetics)
1Adult
1Algorithms
1Calcium-Binding Proteins (genetics)
1Child
1Child, Preschool
1Connexin 43 (genetics)
1Diagnosis, Differential
1Exons
1Eye Abnormalities (diagnosis)
1Eye Abnormalities (genetics)
1Fetus
1Foot Deformities, Congenital (diagnosis)
1Foot Deformities, Congenital (genetics)
1Genetic Predisposition to Disease
1Genital Diseases, Male (diagnosis)
1Genital Diseases, Male (genetics)
1Hydrops Fetalis (diagnosis)
1Hydrops Fetalis (genetics)
1Infant
1Infant, Newborn
1Lymphangiectasis, Intestinal (diagnosis)
1Lymphangiectasis, Intestinal (genetics)
1Lymphatic Abnormalities (diagnosis)
1Lymphatic Abnormalities (genetics)
1Lymphedema (classification)
1Lymphoscintigraphy
1Male
1Pedigree
1Phenotype
1Syndactyly (diagnosis)
1Syndactyly (genetics)
1Tooth Abnormalities (diagnosis)
1Tooth Abnormalities (genetics)
1Tumor Suppressor Proteins (genetics)

Pour manipuler ce document sous Unix (Dilib)

EXPLOR_STEP=$WICRI_ROOT/Wicri/Sante/explor/LymphedemaV1/Data/UK/Analysis
HfdIndexSelect -h $EXPLOR_AREA/Data/UK/Analysis/Author.i -k "Ps Mortimer" 
HfdIndexSelect -h $EXPLOR_AREA/Data/UK/Analysis/Author.i  \
                -Sk "Ps Mortimer" \
         | HfdSelect -Kh $EXPLOR_AREA/Data/UK/Analysis/biblio.hfd 

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   |clé=    Ps Mortimer
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