List of bibliographic references
Number of relevant bibliographic references: 10.
List of associated KwdEn.i
Nombre de documents | Descripteur |
1 | AML, acute myeloid leukaemia |
1 | Aicardi syndrome |
1 | Aortic Coarctation (complications) |
1 | Aortic Coarctation (genetics) |
1 | Aortic Coarctation (pathology) |
1 | CDKL5 early‐onset seizures |
1 | CMP, cardiomyopathy |
1 | CNS, central nervous system |
1 | Ectodermal Dysplasia (complications) |
1 | Ectodermal Dysplasia (genetics) |
1 | Ectodermal Dysplasia (pathology) |
1 | Female |
1 | Genetic Predisposition to Disease |
1 | Humans |
1 | Infant, Newborn |
1 | LEOPARD syndrome |
1 | LS, LEOPARD syndrome |
1 | MVP, mitral valve prolapse |
1 | NS, Noonan syndrome |
1 | Noonan syndrome |
1 | OFD 1 |
1 | OFD1 |
1 | OFD1, oral–facial–digital syndrome type 1 |
1 | PKD, polycystic kidney disease |
1 | PS, pulmonary stenosis |
1 | PTPN11 |
1 | Rett syndrome features |
1 | aortic coarctation |
1 | dominant X linked mode of inheritance |
1 | ectodermal dysplasia |
1 | encéphalopathie myoclonique précoce |
1 | epilepsy, myoclonus |
1 | glycine |
1 | gènes dominant |
1 | hyperglycinémie sans cétose |
1 | infant, newborn |
1 | infantile spasms |
1 | lentigines |
1 | neuroregulators |
1 | neurotransmetteurs |
1 | polyaplic kidney disease |
1 | scalp |
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EXPLOR_STEP=$WICRI_ROOT/Wicri/France/explor/LeHavreV1/Data/France/Analysis
HfdIndexSelect -h $EXPLOR_AREA/Data/France/Analysis/Author.i -k "V. Layet"
HfdIndexSelect -h $EXPLOR_AREA/Data/France/Analysis/Author.i \
-Sk "V. Layet" \
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|étape= Analysis
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|index= Author.i
|clé= V. Layet
}}
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