Russell-Silver syndrome

American Journal of Medical Genetics, Part C: Seminars in Medical Genetics

Volumn 154, Issue 3, 2010, Pages 355-364

  Eggermann, Thomas ^a  

^a NONE

Author keywords

11p15 epimutation; Genetic testing; Multilocus loss of methylation; Russell Silver syndrome; UPD(7)mat

Indexed keywords

BIRTH; CHROMOSOME 7; CHROMOSOME REARRANGEMENT; CLINICAL FEATURE; CLINODACTYLY; DEVELOPMENTAL DISORDER; DNA METHYLATION; DOWN REGULATION; EAR MALFORMATION; EPIGENETICS; FACE MALFORMATION; FOREHEAD; GENE LOCUS; GENETIC COUNSELING; GENETIC DISORDER; GENETIC SCREENING; GENOME IMPRINTING; GENOTYPE PHENOTYPE CORRELATION; GROWTH RETARDATION; HUMAN; INTRAUTERINE GROWTH RETARDATION; KARYOTYPING; MACROCEPHALY; METHYLATION; MICROGNATHIA; MUSCLE HYPOTONIA; PRIORITY JOURNAL; RECURRENCE RISK; REPRODUCTION; REVIEW; SCORING SYSTEM; SILVER RUSSELL SYNDROME; TOOTH MALFORMATION; UNIPARENTAL DISOMY; CHROMOSOME 11; CHROMOSOME ABERRATION; GENETIC ASSOCIATION; GENETICS; MUTATION;

CHROMOSOME ABERRATIONS; CHROMOSOMES, HUMAN, PAIR 11; DNA METHYLATION; FETAL GROWTH RETARDATION; GENETIC ASSOCIATION STUDIES; GENETIC TESTING; GENOMIC IMPRINTING; HUMANS; KARYOTYPING; MUTATION; SILVER-RUSSELL SYNDROME; UNIPARENTAL DISOMY;

EID: 77955860624     PISSN: 15524868     EISSN: 15524876     Source Type: Journal    
DOI: 10.1002/ajmg.c.30274     Document Type: Review

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