Cryptic familial t(11;18)(q25;q23) incidentally detected by interphase FISH

Clinical Genetics

Volumn 59, Issue 4, 2001, Pages 279-283

  Schultz, Ln ^a   Schmidt, P ^a   Tabor, A ^b   Bryndorf, T ^a   Christensen, B ^a   Lundsteen, C ^a  

^a Rigshospitalet   (Denmark)

^b HVIDOVRE HOSPITAL   (Denmark)

Author keywords

18qter probe; Cryptic translocation; FISH; Prenatal diagnosis

Indexed keywords

ADULT; ARTICLE; BODY DYSMORPHIC DISORDER; CASE REPORT; CHORION VILLUS SAMPLING; CHROMOSOME 11Q; CHROMOSOME 13; CHROMOSOME 18Q; CHROMOSOME 21; CHROMOSOME G BAND; CHROMOSOME TRANSLOCATION 11; CHROMOSOME TRANSLOCATION 18; CONTROLLED STUDY; CYTOGENETICS; FAMILIAL DISEASE; FAMILY; FEMALE; FETUS; FLUORESCENCE IN SITU HYBRIDIZATION; FOLLOW UP; GENE LOCUS; GENE PROBE; HUMAN; HUMAN CELL; HUMAN TISSUE; INTERPHASE; KARYOTYPE; KARYOTYPE 46,XX; MALE; MENTAL DEFICIENCY; MOLECULAR GENETICS; NUMERICAL CHROMOSOME ABERRATION; PEDIGREE; PRENATAL SCREENING; PRIORITY JOURNAL; PROSPECTIVE STUDY; TELOMERE; X CHROMOSOME; Y CHROMOSOME;

ABNORMALITIES, MULTIPLE; ADOLESCENT; CHROMOSOMES, HUMAN, PAIR 11; CHROMOSOMES, HUMAN, PAIR 18; FEMALE; HETEROZYGOTE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INTERPHASE; MALE; PEDIGREE; PROSPECTIVE STUDIES; TRANSLOCATION, GENETIC;

RAPHIA FRATER;

EID: 0035050576     PISSN: 00099163     EISSN: None     Source Type: Journal    
DOI: 10.1034/j.1399-0004.2001.590411.x     Document Type: Article

References (15)

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12. Detection of a cryptic translocation in a family with mental retardation using FISH and telomere region-specific probes
13. Prenatal diagnosis of a mosaic extra structurally abnormal chromosome by spectral karyotyping
14. Characterization of a de novo partial trisomy 22q13-qter in a patient by microFISH
15. Prenatal detection of chromosome aneuploidies in uncultured chorionic villus samples by FISH