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Volumn 4, Issue 2, 1996, Pages 88-100
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Clinical heterogeneity in 16 patients with inv dup 15 chromosome: Cytogenetic and molecular studies, search for an imprinting effect
a |
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Author keywords
Imprinting; inv dup (15) marker breakpoints; Methylation status; Parental origin
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Indexed keywords
ADOLESCENT;
ADULT;
ARTICLE;
CHILD;
CHROMOSOME 15;
CHROMOSOME DUPLICATION;
CHROMOSOME INVERSION;
CLINICAL ARTICLE;
CONTROLLED STUDY;
CYTOGENETICS;
DISEASE SEVERITY;
DNA METHYLATION;
EPILEPSY;
FEMALE;
GENETIC HETEROGENEITY;
GENOME IMPRINTING;
GENOTYPE;
HUMAN;
HUMAN CELL;
KARYOTYPE;
MALE;
MARKER GENE;
MEIOSIS;
MOLECULAR BIOLOGY;
PHENOTYPE;
PRIORITY JOURNAL;
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EID: 0029960187
PISSN: 10184813
EISSN: None
Source Type: Journal
DOI: 10.1159/000472176 Document Type: Article |
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Times cited : (67)
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References (1)
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