Interstitial deletion of 13q and a 13;X chromosome translocation results in partial trisomy 13 and bilateral retinoblastoma

Ophthalmic Genetics

Volumn 24, Issue 3, 2003, Pages 175-180

  Dries, David ^a   Baca, Katrina ^b   Truss, Lisa ^b   Dobin, Sheila ^b  

^a UNIVERSITY OF UTAH SCHOOL OF MEDICINE   (United States)

^b TEXAS A M COLLEGE OF MEDICINE   (United States)

Author keywords

Chromosome X; Retinoblastoma; Trisomy 13; Unbalanced translocation; X inactivation

Indexed keywords

ARTICLE; BONE MARROW; CALCIFICATION; CASE REPORT; CHROMOSOME 13Q; CHROMOSOME ABERRATION; CHROMOSOME DELETION 13; CHROMOSOME TRANSLOCATION X; DEVELOPMENTAL DISORDER; FACIES; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE EXPRESSION; GENE LOCUS; HETEROZYGOSITY LOSS; HUMAN; HUMAN CELL; INTERSTITIAL CHROMOSOME DELETION; KARYOTYPE; OPHTHALMOSCOPY; PARTIAL TRISOMY 13; PRESCHOOL CHILD; PRIORITY JOURNAL; RETINOBLASTOMA; SEIZURE; TUMOR SUPPRESSOR GENE; X CHROMOSOME INACTIVATION;

CHROMOSOME ABERRATIONS; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 13; CHROMOSOMES, HUMAN, X; FEMALE; GROWTH DISORDERS; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT; MALE; MENTAL RETARDATION; RETINAL NEOPLASMS; RETINOBLASTOMA; TRANSLOCATION, GENETIC; TRISOMY;

EID: 0041704756     PISSN: 13816810     EISSN: None     Source Type: Journal    
DOI: 10.1076/opge.24.3.175.15612     Document Type: Article

References (13)

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