List of bibliographic references
Number of relevant bibliographic references: 1.
List of associated KwdEn.i
Nombre de
documents | Descripteur |
|---|
| 1 | Amplification |
| 1 | Array CGH |
| 1 | BAC, bacterial artificial chromosome |
| 1 | Browser |
| 1 | CGH, comparative genomic hybridisation |
| 1 | CNP, copy number polymorphism |
| 1 | Causative |
| 1 | Causative duplications |
| 1 | Chromosomal |
| 1 | Chromosomal aberrations |
| 1 | Chromosomal copy number changes |
| 1 | Chromosome |
| 1 | Clone |
| 1 | Cnps |
| 1 | Comparative genomic hybridisation |
| 1 | Copy number |
| 1 | Copy number changes |
| 1 | Copy number gain |
| 1 | Copy number polymorphisms |
| 1 | Deletion |
| 1 | Diagnostic tool |
| 1 | Duplication |
| 1 | Dysmorphic features |
| 1 | FISH, fluorescent in situ hybridisation |
| 1 | FSIQ, full scale intelligence quotient |
| 1 | Family members |
| 1 | Full coverage |
| 1 | Gene |
| 1 | Genet |
| 1 | Genetic disease |
| 1 | Genetics |
| 1 | Genome |
| 1 | Genomic |
| 1 | Genomic polymorphism |
| 1 | Genomic polymorphisms |
| 1 | High copy numbers |
| 1 | Human |
| 1 | Human genetics |
| 1 | Hybridisation |
| 1 | Index patient |
| 1 | Large duplication |
| 1 | Linkage |
| 1 | Linkage interval |
| 1 | Log2 |
| 1 | Log2 ratio |
| 1 | Lugtenberg |
| 1 | Lymphoblastoid cell lines |
| 1 | MLPA |
| 1 | MLPA, multiplex ligated probe amplification |
| 1 | MR, mental retardation |
| 1 | MRX, non-syndromic X linked mental retardation |
| 1 | MRXS, syndromic X linked mental retardation |
| 1 | Mecp2 |
| 1 | Mecp2 gene |
| 1 | Mental retardation |
| 1 | Mlpa |
| 1 | Mlpa analysis |
| 1 | Mlpa probes |
| 1 | More insight |
| 1 | Mutation |
| 1 | Normal copy numbers |
| 1 | Patient |
| 1 | Polymorphism |
| 1 | Probe |
| 1 | Rearrangement |
| 1 | Retardation |
| 1 | STS, sequence tagged site |
| 1 | Segmental |
| 1 | Segmental duplication |
| 1 | Segmental duplications |
| 1 | Sex linked character |
| 1 | T/R, test over reference |
| 1 | Ucsc |
| 1 | Ucsc genome browser |
| 1 | Variable regions |
| 1 | X-Chromosome |
| 1 | XLMR |
| 1 | XLMR, X linked mental retardation |
| 1 | Xlmr |
| 1 | Xlmr genes |
| 1 | copy number polymorphisms (CNPs) |
| 1 | duplications |
Pour manipuler ce document sous Unix (Dilib)
EXPLOR_STEP=$WICRI_ROOT/Wicri/Asie/explor/AustralieFrV1/Data/Allemagne/Analysis
HfdIndexSelect -h $EXPLOR_AREA/Data/Allemagne/Analysis/Author.i -k "C T R M. Schrander-Stumpel"
HfdIndexSelect -h $EXPLOR_AREA/Data/Allemagne/Analysis/Author.i \
-Sk "C T R M. Schrander-Stumpel" \
| HfdSelect -Kh $EXPLOR_AREA/Data/Allemagne/Analysis/biblio.hfd
Pour mettre un lien sur cette page dans le réseau Wicri
{{Explor lien
|wiki= Wicri/Asie
|area= AustralieFrV1
|flux= Allemagne
|étape= Analysis
|type= indexItem
|index= Author.i
|clé= C T R M. Schrander-Stumpel
}}
| This area was generated with Dilib version V0.6.33.
Data generation: Tue Dec 5 10:43:12 2017. Site generation: Tue Mar 5 14:07:20 2024 |  |
