Functional mosaic trisomy of 1q12→1q21 resulting from X-autosome insertion translocation with random inactivation

Clinical Genetics

Volumn 54, Issue 1, 1998, Pages 70-73

  Vust, A ^a   Riordan, D ^a   Wickstrom, D ^a   Chudley, A E ^a   Dawson, A J ^a,b  

^a UNIVERSITY OF MANITOBA   (Canada)

^b Cytogenetics Laboratory   (Canada)

Author keywords

FISH; Functional mosaic; Random X inactivation; Trisomy 1q12 1q21

Indexed keywords

ADOLESCENT; ARTICLE; CASE REPORT; CHROMOSOME 1Q; CHROMOSOME MOSAICISM; CHROMOSOME REPLICATION; CHROMOSOME XQ; EUCHROMATIN; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HETEROCHROMATIN; HUMAN; HUMAN CELL; INSERTIONAL CHROMOSOME TRANSLOCATION; KARYOTYPE; PRIORITY JOURNAL; TRISOMY; X CHROMOSOME INACTIVATION;

EID: 0031927901     PISSN: 00099163     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1399-0004.1998.tb03697.x     Document Type: Article

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