Amplification of a pseudogene cassette underlies enchromatic variation of 16p at the cytogenetic level

Human Genetics

Volumn 104, Issue 3, 1999, Pages 211-218

  Barber, John C K ^a   Reed, Caroline J ^a   Dahoun, Sophie P ^b   Joyce, Christine A ^a  

^a SALISBURY DISTRICT HOSPITAL   (United Kingdom)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

CARRIER PROTEIN; IMMUNOGLOBULIN HEAVY CHAIN;

ADULT; ARTICLE; CASE REPORT; CHROMOSOME 16P; CONTROLLED STUDY; COSMID; CYTOGENETICS; EUCHROMATIN; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE AMPLIFICATION; GENE CASSETTE; GENETIC VARIABILITY; HETEROZYGOTE; HUMAN; IMMUNOGLOBULIN GENE; MALE; PRIORITY JOURNAL; PSEUDOGENE;

ADOLESCENT; ADULT; CHILD, PRESCHOOL; CHROMATIN; CHROMOSOME BANDING; CHROMOSOMES, HUMAN, PAIR 16; EUCHROMATIN; FEMALE; GENE AMPLIFICATION; HUMANS; IMMUNOGLOBULIN HEAVY CHAINS; IMMUNOGLOBULIN VARIABLE REGION; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT; INFANT, NEWBORN; KARYOTYPING; MALE; MIDDLE AGED; PSEUDOGENES; VARIATION (GENETICS);

EID: 0032908833     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004390050938     Document Type: Article

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