Severe hemihypotrophy in a female infant with mosaic Turner syndrome: A variant of Russell-Silver syndrome?

Clinical Dysmorphology

Volumn 13, Issue 2, 2004, Pages 95-98

  Li, Chumei C ^a   Chodirker, Bernard N ^a   Dawson, Angelika J ^a,b   Chudley, Albert E ^a,c  

^a UNIVERSITY OF MANITOBA   (Canada)

^b HEALTH SCIENCES CENTRE   (Canada)

^c Dept of Pediatrics and Child Health   (Canada)

Author keywords

Chromosome anomaly; Hemihypotrophy; Mosaicism; Russell Silver syndrome; Turner syndrome

Indexed keywords

AMNION CELL; ARTICLE; BONE MALFORMATION; CASE REPORT; CELL CULTURE; CLINICAL FEATURE; DELIVERY; EYE; FACE MALFORMATION; FACIES; FEMALE; FINGER MALFORMATION; FOREHEAD; GENETIC HETEROGENEITY; HUMAN; HYPOPLASIA; HYPOTROPHY; INFANT; JAW MALFORMATION; KARYOTYPE; LIP MALFORMATION; MALFORMATION SYNDROME; MOSAIC TURNER SYNDROME; MOUTH; NOSE; PHENOTYPE; PRIORITY JOURNAL; SILVER RUSSELL SYNDROME; SKIN FIBROBLAST; STATISTICAL SIGNIFICANCE; TURNER SYNDROME; ZYGOMA; GENETIC VARIABILITY; MOSAICISM; SYNDROME; UNIPARENTAL DISOMY;

FEMALE; HUMANS; INFANT; MOSAICISM; SYNDROME; TURNER SYNDROME; UNIPARENTAL DISOMY; VARIATION (GENETICS);

EID: 7444246707     PISSN: 09628827     EISSN: None     Source Type: Journal    
DOI: 10.1097/00019605-200404000-00008     Document Type: Article

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