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American Journal of Medical Genetics

Volumn 93, Issue 5, 2000, Pages 393-398

Tetrasomy 15q25→qter: Cytogenetic and molecular characterization of an analphoid supernumerary marker chromosome

(5) Rowe, Amy G a Abrams, Liane a Qu, Yong b Chen, Emily a Cotter, Philip D a

a CHILDREN S HOSPITAL OAKLAND (United States)

b Chapman Inst of Medical Genetics (United States)

Author keywords

Centromere; Chromosome 15; Supernumerary marker chromosome; Tetrasomy

Indexed keywords

ARTICLE; CASE REPORT; CHROMOSOME 15Q; CHROMOSOME C BAND; CHROMOSOME MOSAICISM; CHROMOSOME PAINTING; CHROMOSOME POLYMORPHISM; CYTOGENETICS; DICENTRIC CHROMOSOME; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; HUMAN CELL; MARKER CHROMOSOME; MEIOSIS; MENTAL RETARDATION MALFORMATION SYNDROME; METAPHASE CHROMOSOME; MOLECULAR GENETICS; PRIORITY JOURNAL; SCHOOL CHILD; SUPERNUMERARY CHROMOSOME; TETRASOMY; ALLELE; CHILD; CHROMOSOME 15; CHROMOSOME ABERRATION; CHROMOSOME ANALYSIS; GENETIC MARKER; GENETICS; GENOTYPE; MALE; METHODOLOGY; MULTIPLE MALFORMATION SYNDROME;

ABNORMALITIES, MULTIPLE; ALLELES; CHILD; CHROMOSOME ABERRATIONS; CHROMOSOMES, HUMAN, PAIR 15; CYTOGENETIC ANALYSIS; FEMALE; GENETIC MARKERS; GENOTYPE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; MALE;

EID: 0034726166 PISSN: 01487299 EISSN: None Source Type: Journal
DOI: 10.1002/1096-8628(20000828)93:5<393::AID-AJMG9>3.0.CO;2-Z Document Type: Article

Times cited : (33)

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