Androgenetic/biparental mosaicism in a girl with Beckwith-Wiedemann syndrome-like and upd(14)pat-like phenotypes

Journal of Human Genetics

Volumn 56, Issue 1, 2011, Pages 91-93

  Yamazawa, Kazuki ^a,c   Nakabayashi, Kazuhiko ^a   Matsuoka, Kentaro ^b   Masubara, Keiko ^a   Hata, Kenichiro ^a   Horikawa, Reiko ^b   Ogata, Tsutomu ^a  

^a NATIONAL RESEARCH INSTITUTE FOR CHILD HEALTH AND DEVELOPMENT   (Japan)

^b NATIONAL CENTER FOR GLOBAL HEALTH AND MEDICINE   (Japan)

^c UNIVERSITY OF CAMBRIDGE   (United Kingdom)

Author keywords

androgenesis; Beckwith Wiedemann syndrome; mosaicism; upd(14)pat

Indexed keywords

MICROSATELLITE DNA;

ARTICLE; BECKWITH WIEDEMANN SYNDROME; BLASTOMERE; CASE REPORT; CELL DIVISION; CELL LINEAGE; CHILD; EPIGENETICS; FATHER; FEMALE; FERTILIZATION; GENE EXPRESSION; GENE FREQUENCY; GENE LOCUS; GENETIC ASSOCIATION; HUMAN; HUMAN TISSUE; LEUKOCYTE COUNT; MALE TYPE ALOPECIA; METHYLATION; MITOSIS; MOTHER; OOCYTE; PHENOTYPE; PRESCHOOL CHILD; PRONUCLEUS; SPERM; TONGUE; TONSIL; UNIPARENTAL DISOMY;

BECKWITH-WIEDEMANN SYNDROME; CHILD, PRESCHOOL; CHROMOSOMES, HUMAN, PAIR 14; FEMALE; HUMANS; MOSAICISM; PHENOTYPE; UNIPARENTAL DISOMY;

EID: 79251645149     PISSN: 14345161     EISSN: None     Source Type: Journal    
DOI: 10.1038/jhg.2010.142     Document Type: Article

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