Detection of a subtle rearrangement of chromosome 22 using molecular techniques

American Journal of Medical Genetics

Volumn 58, Issue 4, 1995, Pages 389-394

  Biesecker, L G ^a   Rosenberg, M ^a   Dziadzio, L ^a   Ledbetter, D H ^a   Ning, Y ^a   Sarneso, C ^a   Rosenbaum, K ^a  

^a NATIONAL HUMAN GENOME RESEARCH INSTITUTE   (United States)

Author keywords

chromosome 22; dinucleotide repeat polymorphisms; multiple abnormalities; pericentric inversion

Indexed keywords

DNA;

ARTICLE; CASE REPORT; CHILD; CHROMOSOME 22Q; CHROMOSOME DUPLICATION; CHROMOSOME MARKER; CHROMOSOME REARRANGEMENT; CHROMOSOME SATELLITE; CHROMOSOME TRANSLOCATION; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; HUMAN CELL; MULTIPLE MALFORMATION SYNDROME; PRIORITY JOURNAL; TELOMERE; TRISOMY;

ABNORMALITIES, MULTIPLE; BRAIN; CASE REPORT; CHILD; CHROMOSOME ABERRATIONS; CHROMOSOME DISORDERS; CHROMOSOMES, HUMAN, PAIR 22; CLEFT LIP; CLEFT PALATE; FEMALE; GROWTH DISORDERS; HUMAN; HYPERTELORISM; IN SITU HYBRIDIZATION, FLUORESCENCE; MENTAL RETARDATION; MICROSATELLITE REPEATS; MUSCLE HYPOTONIA; SEIZURES; TRANSLOCATION (GENETICS); TRISOMY;

EID: 0029068708     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.1320580426     Document Type: Article

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