Mosaic trisomy 13: Understanding origin using SNP array

Journal of Medical Genetics

Volumn 48, Issue 5, 2011, Pages 323-326

  Jinawath, Natini ^a,b   Zambrano, Regina ^a,c   Wohler, Elizabeth ^d   Palmquist, Maria K ^a,e   Hoover Fong, Julie ^a   Hamosh, Ada ^a   Batista, Denise A S ^a,d  

^a DEPARTMENT OF PATHOLOGY   (United States)

^b MAHIDOL UNIVERSITY   (Thailand)

^c LOUISIANA STATE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^d KENNEDY KRIEGER INSTITUTE   (United States)

^e UNIVERSITY OF SOUTH DAKOTA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ANAPHASE; ANEUPLOIDY; ARTICLE; BIOINFORMATICS; CASE REPORT; CHROMOSOME 13; CROSSING OVER; DISOMY; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE FREQUENCY; GENETIC VARIABILITY; HUMAN; MALE; MEIOSIS; MITOSIS; MOSAICISM; PRIORITY JOURNAL; RISK ASSESSMENT; SINGLE NUCLEOTIDE POLYMORPHISM; TRISOMY 13;

ADULT; CHROMOSOME DISORDERS; CHROMOSOMES, HUMAN, PAIR 13; FEMALE; HUMANS; INFANT; MALE; MEIOSIS; MITOSIS; MOSAICISM; NONDISJUNCTION, GENETIC; OLIGONUCLEOTIDE ARRAY SEQUENCE ANALYSIS; PHENOTYPE; POLYMORPHISM, SINGLE NUCLEOTIDE; TRISOMY;

EID: 79955533966     PISSN: 00222593     EISSN: 14686244     Source Type: Journal    
DOI: 10.1136/jmg.2010.083931     Document Type: Article

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