Clinical-etiologic correlation in children with Prader-Willi syndrome (PWS): An interdisciplinary study

American Journal of Medical Genetics, Part A

Volumn 143, Issue 5, 2007, Pages 460-468

  Torrado, Maria ^a   Araoz, Veronica ^a   Baialardo, Edgardo ^a   Abraldes, Karina ^a   Mazza, Carmen ^a   Krochik, Gabriela ^a   Ozuna, Blanca ^a   Leske, Vivian ^a   Caino, Silvia ^a   Fano, Virginia ^a   Chertkoff, Lilien ^a  

^a HOSPITAL DE PEDIATRÍA PROF DR JUAN P GARRAHAN   (Argentina)

Author keywords

Glucose metabolism; IQ; Phenotype genotype correlation; Polysomnography; Prader Willi syndrome

Indexed keywords

ARTICLE; CARBOHYDRATE METABOLISM; CAUSAL ATTRIBUTION; CHROMOSOME 15Q; CHROMOSOME DELETION; CLINICAL FEATURE; COGNITION; CONTROLLED STUDY; CORRELATION ANALYSIS; DISEASE ASSOCIATION; FATTY ACID DESATURATION; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; FOOD INTAKE; GENE EXPRESSION; GENETIC ASSOCIATION; GENOTYPE PHENOTYPE CORRELATION; HUMAN; HYPOPIGMENTATION; INTELLIGENCE QUOTIENT; INTERDISCIPLINARY RESEARCH; MAJOR CLINICAL STUDY; MALE; MICROSATELLITE MARKER; PHENOTYPIC VARIATION; POLYSOMNOGRAPHY; PRADER WILLI SYNDROME; PRESCHOOL CHILD; PRIORITY JOURNAL; SLEEP DISORDER; SOUTHERN BLOTTING; SPEECH ARTICULATION; UNIPARENTAL DISOMY;

ADOLESCENT; BODY WEIGHTS AND MEASURES; CARBOHYDRATE METABOLISM; CHILD; CHILD BEHAVIOR; CHILD, PRESCHOOL; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 15; FEMALE; GLUCOSE INTOLERANCE; HUMANS; INFANT; INFANT, NEWBORN; INSULIN RESISTANCE; MALE; PHENOTYPE; PRADER-WILLI SYNDROME; RESEARCH; SLEEP DISORDERS;

EID: 33847341593     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.31520     Document Type: Article

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