List of bibliographic references
Number of relevant bibliographic references: 4.
List of associated KwdEn.i
Nombre de
documents | Descripteur |
|---|
| 4 | Humans |
| 4 | Male |
| 3 | Adult |
| 3 | Female |
| 3 | Nervous system diseases |
| 3 | Nuclear Proteins (genetics) |
| 2 | Chorea |
| 2 | Chorea (genetics) |
| 2 | DNA Mutational Analysis |
| 2 | Family Health |
| 2 | Lung |
| 2 | Lung Diseases (etiology) |
| 2 | Mutation |
| 2 | Phenotype |
| 2 | Thyroid gland |
| 2 | Transcription Factors (genetics) |
| 2 | benign hereditary chorea |
| 1 | Aged |
| 1 | Apoptosis Regulatory Proteins (genetics) |
| 1 | CAG repeat |
| 1 | Caucasoid |
| 1 | Child |
| 1 | Child, Preschool |
| 1 | Chorea (complications) |
| 1 | Chorea (physiopathology) |
| 1 | Chromosomes, Human, Pair 14 |
| 1 | Codon, Terminator (genetics) |
| 1 | DNA-Binding Proteins (genetics) |
| 1 | Deletion |
| 1 | Dementia (genetics) |
| 1 | Dentatorubral |
| 1 | Dentatorubropallidoluysian atrophy |
| 1 | Diagnosis, Differential |
| 1 | Dystonia Musculorum Deformans (genetics) |
| 1 | Dystonia Musculorum Deformans (physiopathology) |
| 1 | Encephalon |
| 1 | Exons (genetics) |
| 1 | Family study |
| 1 | Frameshift Mutation (genetics) |
| 1 | Frameshift mutation |
| 1 | France |
| 1 | French |
| 1 | Gene Deletion |
| 1 | Gene penetrance |
| 1 | Genetic determinism |
| 1 | Genotype |
| 1 | Growth retardation |
| 1 | Huntington Disease (genetics) |
| 1 | In Situ Hybridization, Fluorescence (methods) |
| 1 | Incomplete penetrance |
| 1 | Lung Diseases (genetics) |
| 1 | Mental Disorders (etiology) |
| 1 | Mental Disorders (genetics) |
| 1 | Microsatellite Repeats (genetics) |
| 1 | Middle Aged |
| 1 | Molecular biology |
| 1 | Movement Disorders (genetics) |
| 1 | Mutation (genetics) |
| 1 | Myoclonic Epilepsies, Progressive (complications) |
| 1 | Myoclonic Epilepsies, Progressive (diagnosis) |
| 1 | Myoclonic Epilepsies, Progressive (ethnology) |
| 1 | Myoclonic Epilepsies, Progressive (genetics) |
| 1 | PAX gene |
| 1 | PAX9 Transcription Factor (genetics) |
| 1 | Pallidoluysian atrophy |
| 1 | Pedigree |
| 1 | Psychosis |
| 1 | TITF‐1 |
| 1 | TITF‐1 gene |
| 1 | Thyroid Diseases (etiology) |
| 1 | Tooth Diseases (etiology) |
| 1 | Trinucleotide Repeat Expansion (genetics) |
| 1 | brain‐thyroid‐lung |
| 1 | brain–thyroid–lung syndrome |
| 1 | chorea |
| 1 | movement disorders |
| 1 | thyroid |
Pour manipuler ce document sous Unix (Dilib)
EXPLOR_STEP=$WICRI_ROOT/Wicri/Santé/explor/MovDisordV3/Data/France/Analysis
HfdIndexSelect -h $EXPLOR_AREA/Data/France/Analysis/Author.i -k "Isabelle Vuillaume"
HfdIndexSelect -h $EXPLOR_AREA/Data/France/Analysis/Author.i \
-Sk "Isabelle Vuillaume" \
| HfdSelect -Kh $EXPLOR_AREA/Data/France/Analysis/biblio.hfd
Pour mettre un lien sur cette page dans le réseau Wicri
{{Explor lien
|wiki= Wicri/Santé
|area= MovDisordV3
|flux= France
|étape= Analysis
|type= indexItem
|index= Author.i
|clé= Isabelle Vuillaume
}}
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Data generation: Sun Jul 3 12:29:32 2016. Site generation: Wed Feb 14 10:52:30 2024 |  |
