Assessing implications between genotypic and phenotypic variables through lattice analysis

Behavior Genetics

Volumn 31, Issue 1, 2001, Pages 125-139

  Chabert, Caroline ^a   Cherfouh, Ameziane ^a   Delabar, Jean Maurice ^b   Duquenne, Vincent ^a  

^a CNRS   (France)

^b HÔPITAL NECKER ENFANTS MALADES   (France)

Author keywords

Chromosome 21; Down syndrome; Galois lattice; Implications; Molecular mapping

Indexed keywords

ARTICLE; CHROMOSOME 21; CYTOGENETICS; DOWN SYNDROME; GENE MAPPING; GENOTYPE; HUMAN; MENTAL DEFICIENCY; PHENOTYPE; TRISOMY 21;

CHROMOSOME BANDING; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 21; DOWN SYNDROME; GENOTYPE; HUMANS; MODELS, GENETIC; PHENOTYPE;

EID: 0034881757     PISSN: 00018244     EISSN: None     Source Type: Journal    
DOI: 10.1023/A:1010270211671     Document Type: Article

References (11)

1. Molecular mapping of twenty-four features of Down Syndrome on chromosome 21
2. Contextual implications between attributes and some representation properties for finite lattices
3. Lattice analysis and the representation of handicap association
4. Towards an intensional logic of features
5. Latticial structures in data analysis
6. Protocols to establish genotype-phenotype correlations in Down syndrome
7. Molecular definition of a region of chromosome 21 that causes features of the Down syndrome phenotype
8. Down syndrome: Molecular mapping of the congenital heart disease and duodenal stenosis
9. Down syndrome phenotypes: The consequence of chromosomal imbalance
10. Construction of a panel of transgenic mice containing a contiguous 2-Mb set of YACIPI clones from human chromosome 21q22.2