Clinical and molecular findings in two patients with Russell-Silver syndrome and UPD7: Comparison with non-UPD7 cases

American Journal of Medical Genetics

Volumn 87, Issue 3, 1999, Pages 230-236

  Bernard, L E ^a   Penaherrera M S ^b   Van Allen, M I ^a   Wang, M S ^b   Yong, S L ^a   Gareis, F ^c   Langlois, S ^a   Robinson, W P ^b,d  

^a BC CHILDREN S HOSPITAL   (Canada)

^b CHILDREN S AND WOMEN S HEALTH CENTRE OF BRITISH COLUMBIA   (Canada)

^c CHILDREN S HOSPITAL OAKLAND   (United States)

^d UNIVERSITY OF BRITISH COLUMBIA   (Canada)

Author keywords

Russell Silver syndrome; Short stature; Silver Russell syndrome; Uniparental disomy

Indexed keywords

ARTICLE; CHILD; CHROMOSOME 7; CHROMOSOME DELETION; DISEASE ASSOCIATION; FEMALE; GENETIC ANALYSIS; GROWTH RETARDATION; HUMAN; INFANT; MACROCEPHALY; MALE; PHENOTYPE; POINT MUTATION; PRIORITY JOURNAL; SILVER RUSSELL SYNDROME; UNIPARENTAL DISOMY;

ABNORMALITIES, MULTIPLE; ADULT; CAFE-AU-LAIT SPOTS; CHROMOSOME ABERRATIONS; CHROMOSOME DISORDERS; CHROMOSOMES, HUMAN, PAIR 7; DENTAL ENAMEL HYPOPLASIA; FACIES; FEMALE; FINGERS; GENOMIC IMPRINTING; GROWTH DISORDERS; HEAD; HUMANS; INFANT, NEWBORN; LEARNING DISORDERS; MALE; PHENOTYPE; SYNDROME; TOOTH ABNORMALITIES;

EID: 0344541708     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19991126)87:3<230::AID-AJMG7>3.0.CO;2-S     Document Type: Article

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