Molecular characterization of a ring chromosome 16 from a patient with bilateral cataracts

American Journal of Medical Genetics

Volumn 107, Issue 1, 2002, Pages 12-17

  He, W ^a   Tuck Muller, C M ^a   Martinez J E ^a   Li, S ^a   Rowley, E R ^a   Wertelecki, W ^a  

^a UNIVERSITY OF OKLAHOMA COLLEGE OF MEDICINE   (United States)

Author keywords

Cataracts; Fluorescence in situ hybridization (FISH); Polymerase chain reaction (PCR); Ring chromosome 16

Indexed keywords

ARTICLE; CASE REPORT; CATARACT; CHROMOSOME 16; CHROMOSOME BREAKAGE; CHROMOSOME DELETION; CHROMOSOME DELETION 16; CLINICAL FEATURE; CYTOGENETICS; DEVELOPMENTAL DISORDER; DISEASE COURSE; EXTRACHROMOSOMAL INHERITANCE; FACE DYSMORPHIA; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE LOCUS; GENETIC ASSOCIATION; HUMAN; INFANT; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; RING CHROMOSOME;

CATARACT; CHROMOSOMES, HUMAN, PAIR 16; CYTOGENETIC ANALYSIS; FEMALE; GENETIC MARKERS; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT; RING CHROMOSOMES;

EID: 0036134797     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.10091     Document Type: Article

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