Disclosing the mechanisms of origin of de novo short-arm duplications of chromosome 9

American Journal of Medical Genetics

Volumn 117 A, Issue 1, 2003, Pages 41-46

  Krepischi Santos, Ana Cristina V ^a   Vianna Morgante, Angela M ^a  

^a UNIVERSITY OF SÃO PAULO   (Brazil)

Author keywords

Chromatid rearrangement; Chromosome 9p duplication; De novo tandem duplication

Indexed keywords

MICROSATELLITE DNA; DNA;

ADOLESCENT; ALLELE; ARTICLE; CASE REPORT; CENTROMERE; CHILD; CHROMATID EXCHANGE; CHROMOSOME 9P; CHROMOSOME ARM; CHROMOSOME DUPLICATION; CHROMOSOME REARRANGEMENT; CLINICAL FEATURE; CLINODACTYLY; CRANIOFACIAL MALFORMATION; CRYPTORCHISM; EPICANTHUS; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; FRONTAL BOSSING; GENE LOCUS; GENE MAPPING; GENE SEQUENCE; GENETIC RECOMBINATION; GENITAL MALFORMATION; GENOTYPE; HIRSUTISM; HOMOZYGOSITY; HUMAN; HYPERTELORISM; KYPHOSIS; MALE; MENTAL DEFICIENCY; MICROCEPHALY; NAIL HYPOPLASIA; NUCLEOTIDE REPEAT; PHALANX HYPOPLASIA; PRIORITY JOURNAL; RETROGNATHIA; SCOLIOSIS; SEQUENCE ANALYSIS; SEQUENCE HOMOLOGY; SHORT STATURE; SYMPTOM; TELOMERE; ZYGOTE; CHROMOSOME 9; CHROMOSOME ABERRATION; CONTIG MAPPING; GENE DUPLICATION; GENETICS;

ADOLESCENT; CHILD; CHROMOSOME ABERRATIONS; CHROMOSOMES, HUMAN, PAIR 9; CONTIG MAPPING; DNA; FEMALE; GENE DUPLICATION; GENOTYPE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; MALE; MICROSATELLITE REPEATS;

EID: 0038074199     PISSN: 15524825     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.a.10634     Document Type: Article

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