Prader-willi syndrome: Obesity due to genomic imprinting

Current Genomics

Volumn 12, Issue 3, 2011, Pages 204-215

  Butler, Merlin G ^a  

^a UNIVERSITY OF KANSAS MEDICAL CENTER   (United States)

Author keywords

Angelman syndrome; Clinical presentation and differences; Deletion; Genetic subtypes; Genomic imprinting; Maternal disomy; Prader Willi syndrome

Indexed keywords

GROWTH HORMONE; MELANOCORTIN RECEPTOR; NECDIN; OREXIN; SEROTONIN AGONIST; SMALL NUCLEAR RIBONUCLEOPROTEIN; SMALL NUCLEOLAR RNA;

AGGRESSION; ANGER; ARTICLE; ASPHYXIA; AUTOMUTILATION; CHROMOSOME DELETION; COMPULSIVE PERSONALITY DISORDER; CRYPTORCHISM; DELAYED PUBERTY; DEPRESSION; DIET THERAPY; DIETARY INTAKE; DNA METHYLATION; EARLY DIAGNOSIS; EPIGENETICS; FETUS GROWTH; FORAGING BEHAVIOR; GENE; GENOME IMPRINTING; GROWTH DISORDER; HAPPY PUPPET SYNDROME; HORMONE SUBSTITUTION; HUMAN; HYPERPHAGIA; HYPOGONADISM; HYPOPIGMENTATION; HYPOREFLEXIA; HYPOTHERMIA; INFANTILE HYPOTONIA; INTELLIGENCE QUOTIENT; MACHIAVELLIANISM; MAGEL2 GENE; MKRN3 GENE; MYOPIA; OBESITY; PRADER WILLI SYNDROME; RESPIRATORY DISTRESS; SCOLIOSIS; SLEEP APNEA SYNDROME; SOMNOLENCE; SPEECH ARTICULATION; STRABISMUS; TOOTH MALFORMATION; UNIPARENTAL DISOMY; WEIGHT CONTROL; WEIGHT GAIN;

EID: 79956282385     PISSN: 13892029     EISSN: 18755488     Source Type: Journal    
DOI: 10.2174/138920211795677877     Document Type: Article

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