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Decreased bone mineral density in Prader-Willi syndrome: comparison with obese subjectsExpression of 4 genes between chromosome 15 breakpoints 1 and 2 and behavioral outcomes in Prader-Willi syndromeGhrelin, peptide YY and their receptors: gene expression in brain from subjects with and without Prader-Willi syndrome.Imprinting disorders: non-Mendelian mechanisms affecting growth.Plasma peptide YY and ghrelin levels in infants and children with Prader-Willi syndrome.Benefits and limitations of prenatal screening for Prader-Willi syndrome.Growth Charts for Prader-Willi Syndrome During Growth Hormone Treatment.Prader-Willi Syndrome due to an Unbalanced de novo Translocation t(15;19)(q12;p13.3).Energy expenditure and physical activity in Prader-Willi syndrome: comparison with obese subjects.X-chromosome inactivation patterns in females with Prader-Willi syndrome.Plasma obestatin and ghrelin levels in subjects with Prader-Willi syndrome.
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description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on July 2000
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Prader-Willi Syndrome: Clinical and Genetic Findings
@en
Prader-Willi Syndrome: Clinical and Genetic Findings.
@nl
type
label
Prader-Willi Syndrome: Clinical and Genetic Findings
@en
Prader-Willi Syndrome: Clinical and Genetic Findings.
@nl
prefLabel
Prader-Willi Syndrome: Clinical and Genetic Findings
@en
Prader-Willi Syndrome: Clinical and Genetic Findings.
@nl
P2860
P1433
P1476
Prader-Willi Syndrome: Clinical and Genetic Findings
@en
P2093
Merlin G Butler
Travis Thompson
P2860
P304
P356
10.1097/00019616-200010041-00002
P433
P577
2000-07-01T00:00:00Z