Deletions flanked by breakpoints 3 and 4 on 15p13 may contribute to abnormal phenotypes

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Bibliographic Details
Published inEuropean journal of human genetics : EJHG Vol. 19; no. 5; pp. 547 - 554
Main Authors ROSENFELD, Jill A, STEPHENS, Lindsey E, MERRION, Katrina, MENDOZA-LONDONO, Roberto, DUPUIS, Lucie, SCHULTZ, Roger, TORCHIA, Beth, SAHOO, Trilochan, BEJJANI, Bassem, WEAVER, David D, SHAFFER, Lisa G, COPPINGER, Justine, BALLIF, Blake C, HOO, Joe J, FRENCH, Beatrice N, BANKS, Valerie C, SMITH, Wendy E, MANCHESTER, David, TSAI, Anne Chun-Hui
Format Journal Article
LanguageEnglish
Published Basingstoke Nature Publishing Group 2011
Subjects
Biological and medical sciences
Chromosome aberrations
Fundamental and applied biological sciences. Psychology
General aspects. Genetic counseling
Genetics of eukaryotes. Biological and molecular evolution
Medical genetics
Medical sciences
Molecular and cellular biology
Chromosomal aberration
Breakpoint
Microdeletion
Typing
15q13
Genotype
Boundary value
Chromosome break
Phenotype
segmental duplication
Segmental
genotype―phenotype
Deletion
Abnormal chromosome
Genetics
Chromosome duplication
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ISSN:1018-4813
1476-5438