Silver-Russell syndrome

Archives of Disease in Childhood

Volumn 96, Issue 12, 2011, Pages 1156-1161

  Wakeling, Emma L ^a  

^a NONE

Author keywords

[No Author keywords available]

Indexed keywords

EPSILON SARCOGLYCAN; RECOMBINANT GROWTH HORMONE; TRANSCRIPTION FACTOR FOXP2;

ARTHROGRYPOSIS; CAMPTODACTYLY; CHILD GROWTH; CHROMOSOME 7; CHROMOSOME DUPLICATION; CLINODACTYLY; COGNITIVE DEVELOPMENT; CONGENITAL MALFORMATION; DNA METHYLATION; FACE ASYMMETRY; FEEDING DISORDER; FOLLOW UP; FRONTAL BOSSING; GENE EXPRESSION; GENOTYPE PHENOTYPE CORRELATION; HUMAN; HYPOGLYCEMIA; IDIOPATHIC DISEASE; INSULIN RESISTANCE; INTRAUTERINE GROWTH RETARDATION; LEARNING DISORDER; MICROARRAY ANALYSIS; MICROGNATHIA; MOLECULAR PATHOLOGY; MYOCLONUS DYSTONIA; PRIORITY JOURNAL; PROTEIN EXPRESSION; PSYCHOMOTOR RETARDATION; RECURRENCE RISK; REGULATOR GENE; REVIEW; SILVER RUSSELL SYNDROME; SMALL FOR DATE INFANT; SPEECH DISORDER; SWEATING; UNIPARENTAL DISOMY;

DEVELOPMENTAL DISABILITIES; FACIES; FEEDING BEHAVIOR; GENOMIC IMPRINTING; GENOTYPE; GROWTH DISORDERS; HUMANS; INFANT, NEWBORN; PHENOTYPE; PROGNOSIS; SILVER-RUSSELL SYNDROME; UNIPARENTAL DISOMY;

EID: 81255187962     PISSN: 00039888     EISSN: 14682044     Source Type: Journal    
DOI: 10.1136/adc.2010.190165     Document Type: Review

References (30)

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