Startling mosaicism of the Y-chromosome and tandem duplication of the SRY and DAZ genes in patients with turner syndrome

PLoS ONE

Volumn 3, Issue 11, 2008, Pages

  Premi, Sanjay ^a   Srivastava, Jyoti ^a   Panneer, Ganesan ^a,b   Ali, Sher ^a  

^a NATIONAL INSTITUTE OF IMMUNOLOGY   (India)

^b UNIVERSITY OF LUCKNOW   (India)

Author keywords

[No Author keywords available]

Indexed keywords

PROTEIN DAZ; TESTIS DETERMINING FACTOR; TRANSCRIPTION FACTOR; UNCLASSIFIED DRUG; DAZ1 PROTEIN, HUMAN; RNA BINDING PROTEIN;

APLASIA; ARTICLE; CLINICAL ARTICLE; CLINICAL FEATURE; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE DUPLICATION; GENE MUTATION; GENE SEQUENCE; GENETIC POLYMORPHISM; GENOTYPE; HIGH MOBILITY GROUP BOX DOMAIN; HUMAN; KARYOTYPE 45,X; KARYOTYPE 46,XX; KARYOTYPE 46,XY; MALE; MOSAICISM; OVARY APLASIA; PHENOTYPE; REAL TIME POLYMERASE CHAIN REACTION; TURNER SYNDROME; UTERUS APLASIA; Y CHROMOSOME; ADOLESCENT; ADULT; CHROMOSOME ANALYSIS; GENETICS; PATHOLOGY; SEX CHROMOSOME ABERRATION; SRY GENE; TANDEM REPEAT; UTERUS;

ADOLESCENT; ADULT; CHROMOSOMES, HUMAN, Y; CYTOGENETIC ANALYSIS; FEMALE; GENES, SRY; HUMANS; MOSAICISM; PHENOTYPE; RNA-BINDING PROTEINS; SEX CHROMOSOME ABERRATIONS; TANDEM REPEAT SEQUENCES; TURNER SYNDROME; UTERUS; YOUNG ADULT;

EID: 57049113884     PISSN: None     EISSN: 19326203     Source Type: Journal    
DOI: 10.1371/journal.pone.0003796     Document Type: Article

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