Molecular definition of breakpoints associated with human Xq isochromosomes: Implications for mechanisms of formation

American Journal of Human Genetics

Volumn 58, Issue 1, 1996, Pages 154-160

  Wolff, Daynna J ^a   Miller, Andrew P ^a   Van Dyke, Daniel L ^b   Schwartz, Stuart ^a   Willard, Huntington F ^a,c  

^a UNIVERSITY HOSPITALS OF CLEVELAND   (United States)

^b HENRY FORD HOSPITAL   (United States)

^c CASE WESTERN RESERVE UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CELL LINE; CENTROMERE; CHROMOSOME BREAKAGE; CLINICAL ARTICLE; COSMID; DICENTRIC CHROMOSOME; FIBROBLAST CULTURE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE DUPLICATION; GENE LOCATION; HUMAN; ISOCHROMOSOME X; KARYOTYPE; PRIORITY JOURNAL; SISTER CHROMATID; TURNER SYNDROME;

EID: 0029656085     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (5)

1. Callen DF, Mulley JC, Baker EG, Sutherland GR (1987) Determining the origin of human X isochromosomes by use of DNA sequence polymorphisms and detection of an apparent i(Xq) with Xp sequences. Hum Genet 77:236-240
2. Darlington CD (1939) Misdivision and the genetics of the centromere. J Genet 37:341-364
3. de la Chapelle A, Stenstrand K (1974) Dicentric human X isochromosomes. Hereditas 76:259-268
4. de la Chapelle A, Wennstrom J, Horthing H, Ockey CH (1965) Isochromosome X in man. Part II. Hereditas 54:277-292
5. Earnshaw WC, Cooke CA (1989) Proteins of the inner and outer centromere of mitotic chromosomes. Genome 31:541-552