Genomic imprinting disorders in humans: A mini-review

Journal of Assisted Reproduction and Genetics

Volumn 26, Issue 9-10, 2009, Pages 477-486

  Butler, Merlin G ^a  

^a UNIVERSITY OF KANSAS MEDICAL CENTER   (United States)

Author keywords

Albright hereditary osteodystrophy; Angelman syndrome; Assisted reproductive technology; Beckwith wiedemann syndrome; Dna methylation; Genomic imprinting; Human disorders; Prader willi syndrome; Silverrussell syndrome; Uniparental disomy 14

Indexed keywords

ALBRIGHT SYNDROME; BECKWITH WIEDEMANN SYNDROME; CHROMOSOME 15; CHROMOSOME DELETION; CLINICAL FEATURE; CPG ISLAND; DNA METHYLATION; DNA SEQUENCE; GENE EXPRESSION; GENE LOCATION; GENE LOCUS; GENE MUTATION; GENETIC DISORDER; GENOME IMPRINTING; HAPPY PUPPET SYNDROME; HUMAN; INFERTILITY THERAPY; KARYOTYPE; MORBIDITY; OBESITY; PRADER WILLI SYNDROME; PRIORITY JOURNAL; PSEUDOHYPOPARATHYROIDISM; PSEUDOPSEUDOHYPOPARATHYROIDISM; SHORT SURVEY; SILVER RUSSELL SYNDROME; UNIPARENTAL DISOMY;

ANGELMAN SYNDROME; ANIMALS; BECKWITH-WIEDEMANN SYNDROME; CATTLE; FEMALE; FIBROUS DYSPLASIA, POLYOSTOTIC; GENOMIC IMPRINTING; HUMANS; MALE; PRADER-WILLI SYNDROME; SILVER-RUSSELL SYNDROME; UNIPARENTAL DISOMY;

MAMMALIA; VERTEBRATA;

EID: 77249087062     PISSN: 10580468     EISSN: None     Source Type: Journal    
DOI: 10.1007/s10815-009-9353-3     Document Type: Short Survey

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