Partial hexasomy for the Prader-Willi-Angelman syndrome critical region due to a maternally inherited large supernumerary marker chromosome

American Journal of Medical Genetics, Part A

Volumn 152, Issue 8, 2010, Pages 2034-2038

  Hoppman Chaney, Nicole L ^a   Dawson, D Brian ^a   Nguyen, Lai ^a   Sengupta, Sunanda ^a   Reynolds, Kara ^b   McPherson, Elizabeth ^b   Velagaleti, Gopalrao ^a  

^a MAYO CLINIC   (United States)

^b MARSHFIELD CLINIC   (United States)

Author keywords

Hexasomy; Prader Willi Angelman syndrome critical region; Supernumerary marker chromosome 15; Tricentric

Indexed keywords

ADOLESCENT; ARTICLE; C BANDING; CENTROMERE; CHROMOSOME 15; CHROMOSOME ABERRATION; CHROMOSOME BANDING PATTERN; DEVELOPMENTAL DISORDER; EXTRACHROMOSOMAL INHERITANCE; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENOTYPE; HAPPY PUPPET SYNDROME; HUMAN; INTERPHASE; MARKER CHROMOSOME; METHYLATION; MICROSATELLITE MARKER; MOSAICISM; MULTIPLEX LIGATION DEPENDENT PROBE AMPLIFICATION; NONHUMAN; PARTIAL HEXASOMY; PHENOTYPE; PRADER WILLI SYNDROME; PRIORITY JOURNAL; SEIZURE; SUPERNUMERARY CHROMOSOME;

ADOLESCENT; ANGELMAN SYNDROME; CHROMOSOME ABERRATIONS; CHROMOSOME DISORDERS; CHROMOSOMES, HUMAN, PAIR 15; DNA METHYLATION; FEMALE; GENOMIC IMPRINTING; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; MOSAICISM; MOTHERS; PHENOTYPE; PRADER-WILLI SYNDROME;

EID: 77955296124     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.33483     Document Type: Article

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