Epigenetic anomalies in childhood growth disorders

Nestle Nutrition Institute Workshop Series

Volumn 71, Issue , 2013, Pages 65-73

  Netchine, Irène ^a   Rossignol, Sylvie ^a   Azzi, Salah ^a   Le Bouc, Yves ^a  

^a ASSISTANCE PUBLIQUE HÔPITAUX DE PARIS   (France)

Author keywords

[No Author keywords available]

Indexed keywords

MAMMALIA;

CDKN1C PROTEIN, HUMAN; CYCLIN DEPENDENT KINASE INHIBITOR 1C; KCNQ1 PROTEIN, HUMAN; POTASSIUM CHANNEL KCNQ1; SOMATOMEDIN B;

ALLELE; ARTICLE; BECKWITH WIEDEMANN SYNDROME; CHILD; CHROMOSOME 11; DNA METHYLATION; GENE LOCUS; GENETIC ASSOCIATION; GENETIC EPIGENESIS; GENETICS; GROWTH DISORDER; HUMAN; INFERTILITY THERAPY; INTRAUTERINE GROWTH RETARDATION; METABOLISM; MUTATION; NEWBORN; SILVER RUSSELL SYNDROME; SMALL FOR DATE INFANT;

ALLELES; BECKWITH-WIEDEMANN SYNDROME; CHILD; CHROMOSOMES, HUMAN, PAIR 11; CYCLIN-DEPENDENT KINASE INHIBITOR P57; DNA METHYLATION; EPIGENESIS, GENETIC; FETAL GROWTH RETARDATION; GENETIC ASSOCIATION STUDIES; GENETIC LOCI; GROWTH DISORDERS; HUMANS; INFANT, NEWBORN; INFANT, SMALL FOR GESTATIONAL AGE; INSULIN-LIKE GROWTH FACTOR II; KCNQ1 POTASSIUM CHANNEL; MUTATION; REPRODUCTIVE TECHNIQUES, ASSISTED; SILVER-RUSSELL SYNDROME;

EID: 84885993940     PISSN: 16642147     EISSN: 16642155     Source Type: Book Series    
DOI: 10.1159/000342568     Document Type: Conference Paper

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