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Plant Methods, ISSN 1746-4811, 11/2017, Volume 13, Issue 1, pp. 96 - 12
Background: In maize, silks are hundreds of filaments that simultaneously emerge from the ear for collecting pollen over a period of 1-7 days, which largely... 
Computer vision | Maize | Image-assisted phenotyping | Robot-assisted imaging | Water deficit | Machine learning | SYSTEM | PLANT | KERNEL SET | RECONSTRUCTION | LEAVES | BIOCHEMICAL RESEARCH METHODS | PLANT SCIENCES | TRANSPIRATION | IMAGES | LOWLAND TROPICAL MAIZE | ELONGATION | Phenotype | Usage | Growth | Corn | Physiological aspects | Research | Modeling and Simulation | Computer Science
Journal Article
European journal of human genetics : EJHG, ISSN 1018-4813, 06/2013, Volume 21, Issue 6, pp. 602 - 612
The 2q37 locus is one of the most commonly deleted subtelomeric regions. Such a deletion has been identified in 4100 patients by telomeric fluorescence in situ... 
brachydactyly | AHO-like syndrome | overweight | 2q37-deletion syndrome | intellectual disability | genotype-phenotype correlation | OSTEODYSTROPHY-LIKE PHENOTYPE | MOLECULAR CHARACTERIZATION | AUTISM | PROLACTIN-RELEASING PEPTIDE | BIOCHEMISTRY & MOLECULAR BIOLOGY | CANDIDATE REGION | 2Q37.3 DELETION | GENE | MENTAL-RETARDATION SYNDROME | ARRAY-CGH | GENETICS & HEREDITY | DUPLICATION | Overweight - complications | Humans | Child, Preschool | Intellectual Disability - complications | Male | Intellectual Disability - genetics | Fibrous Dysplasia, Polyostotic - genetics | Young Adult | Chromosomes, Human, Pair 2 - genetics | Adult | Female | Behavior | Fibrous Dysplasia, Polyostotic - complications | Child | Chromosome Deletion | Genetic Association Studies | Chromosome Disorders - complications | Overweight - genetics | Chromosome Mapping | DNA Copy Number Variations - genetics | Comparative Genomic Hybridization | Brachydactyly - genetics | Adolescent | Brachydactyly - complications | Chromosome Disorders - genetics | Intellectual disabilities | Body weight | Hybridization | Gene deletion | French language | Literature reviews | Genotype & phenotype | Databases | Language | Clonal deletion | Cell cycle | Fluorescence in situ hybridization | Genetics | Period 2 protein | Brachydactyly | Genotypes | Seizures | Obesity | Phenotypes | Calpain | Gene expression | Chromosome 2 | Autism | Osteodystrophy | Collaboration | Life Sciences | genotype–phenotype correlation
Journal Article
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