Silver-Russell syndrome

Best Practice and Research: Clinical Endocrinology and Metabolism

Volumn 25, Issue 1, 2011, Pages 153-160

  Binder, Gerhard ^a   Begemann, Matthias ^b   Eggermann, Thomas ^b   Kannenberg, Kai ^a  

^a UNIVERSITY HOSPITAL TÜBINGEN   (Germany)

^b RWTH AACHEN UNIVERSITY   (Germany)

Author keywords

asymmetry; epigenetic; H19; hypomethylation; IGF II; imprinting control region; relative macrocephaly

Indexed keywords

POTASSIUM CHANNEL KCNQ1; RNA H19; SOMATOMEDIN B;

ARTICLE; CHROMOSOME 7P; CHROMOSOME 7Q; CLINODACTYLY; CPG ISLAND; DIFFERENTIAL DIAGNOSIS; DNA METHYLATION; GENE CONTROL; GENE DELETION; GENE EXPRESSION; GENE LOCUS; GENETIC ASSOCIATION; GENETIC COUNSELING; GENETIC PREDISPOSITION; GENETIC SCREENING; GENOME IMPRINTING; HUMAN; HYPOSPADIAS; INTRAUTERINE GROWTH RETARDATION; MACROCEPHALY; MICROSATELLITE MARKER; MULTIPLEX LIGATION DEPENDENT PROBE AMPLIFICATION; POLYMERASE CHAIN REACTION; RECURRENCE RISK; SHORT STATURE; SILVER RUSSELL SYNDROME; UNDERWEIGHT; UNIPARENTAL DISOMY;

EID: 79952492925     PISSN: 1521690X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.beem.2010.06.005     Document Type: Review

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