Parental origin of normal X chromosomes in Turner syndrome patients with various karyotypes: Implications for the mechanism leading to generation of a 45,X karyotype

American Journal of Medical Genetics

Volumn 111, Issue 2, 2002, Pages 134-139

  Uematsu, Ayumi ^a   Yorifuji, Tohru ^a   Muroi, Junko ^a   Kawai, Masahiko ^a   Mamada, Mitsukazu ^a   Kaji, Masayuki ^b   Yamanaka, Chutaro ^c   Momoi, Toru ^d   Nakahata, Tatsutoshi ^a  

^a KYOTO UNIVERSITY HOSPITAL   (Japan)

^b SHIZUOKA CHILDREN'S HOSPITAL   (Japan)

^c TENRI HOSPITAL   (Japan)

^d JAPANESE RED CROSS WAKAYAMA MEDICAL CENTER   (Japan)

Author keywords

Abnormal sex chromosome; Mosaic karyotype; Parental origin; Turner syndrome

Indexed keywords

ARTICLE; CHROMOSOME XQ; CLINICAL ARTICLE; HUMAN; HUMAN TISSUE; ISOCHROMOSOME X; KARYOTYPE; KARYOTYPE 45,X; MEIOSIS; METHYLATION; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; TURNER SYNDROME; X CHROMOSOME; Y CHROMOSOME; CHEMISTRY; DNA METHYLATION; FEMALE; GENETIC MARKER; GENETIC POLYMORPHISM; GENETICS; HETEROZYGOTE; KARYOTYPING; MALE; MOSAICISM; RESTRICTION MAPPING; REVIEW; SEX CHROMOSOME ABERRATION;

CHROMOSOMES, HUMAN, X; CHROMOSOMES, HUMAN, Y; DNA METHYLATION; DNA PRIMERS; FEMALE; GENETIC MARKERS; HETEROZYGOTE; HUMAN; KARYOTYPING; MALE; MICROSATELLITE REPEATS; MOSAICISM; POLYMERASE CHAIN REACTION; POLYMORPHISM (GENETICS); RECEPTORS, ANDROGEN; RESTRICTION MAPPING; SEX CHROMOSOME ABERRATIONS; SUPPORT, NON-U.S. GOV'T; TURNER SYNDROME; HUMANS; POLYMORPHISM, GENETIC;

ANDROGEN RECEPTOR; MICROSATELLITE DNA; PRIMER DNA;

EID: 0037158472     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.10506     Document Type: Article

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