Preface

Cytogenetic and Genome Research

Volumn 135, Issue 3-4, 2011, Pages 171-173

  Poot, Martin ^a  

^a NONE

Author keywords

[No Author keywords available]

Indexed keywords

OLIGONUCLEOTIDE;

ATTENTION DEFICIT DISORDER; AUTISM; COMPARATIVE GENOMIC HYBRIDIZATION; CONGENITAL DISORDER; CONGENITAL HEART DISEASE; COPY NUMBER VARIATION; CYTOGENETICS; DIAGNOSTIC VALUE; EDITORIAL; EXOME; GENE INTERACTION; GENE SEQUENCE; GENERALIZED EPILEPSY; GENETIC ASSOCIATION; GENETIC VARIABILITY; GENOTYPE; GILLES DE LA TOURETTE SYNDROME; HEMATOLOGIC MALIGNANCY; HUMAN; KARYOTYPING; LEUKEMIA; MAJOR DEPRESSION; MENTAL DEFICIENCY; PHENOTYPE; PRIORITY JOURNAL; PSYCHOMOTOR RETARDATION; SCHIZOPHRENIA; SINGLE NUCLEOTIDE POLYMORPHISM; DNA MICROARRAY; GENETIC DISORDER; GENETICS; HUMAN GENOME; LITERATURE;

DNA COPY NUMBER VARIATIONS; GENETIC DISEASES, INBORN; GENETIC VARIATION; GENOME, HUMAN; GENOME-WIDE ASSOCIATION STUDY; HUMANS; OLIGONUCLEOTIDE ARRAY SEQUENCE ANALYSIS; POLYMORPHISM, SINGLE NUCLEOTIDE; REVIEW LITERATURE AS TOPIC;

EID: 83455246331     PISSN: 14248581     EISSN: 14219794     Source Type: Journal    
DOI: 10.1159/000334062     Document Type: Editorial

References (2)

1. Alkan C, Coe BP, Eichler EE: Genome structural variation discovery and genotyping. Nat Rev Genet 12: 363-376 (2011).
2. Vermeesch JR, Melotte C, Froyen G, Van Vooren S, Dutta B, et al: Molecular karyotyping: array CGH quality criteria for constitutional genetic diagnosis. J Histochem Cytochem 53: 413-422 (2005). (Pubitemid 40344086)