|
Volumn 42, Issue 2, 1999, Pages 117-121
|
Biparental expression of IGFBP1 and IGFBP3 renders their involvement in the etiology of Silver-Russell syndrome unlikely
a a a a a a |
Author keywords
IGFBP1; IGFBP3; Imprinting; Maternal uniparental disomy 7; Silver Russell syndrome
|
Indexed keywords
SOMATOMEDIN BINDING PROTEIN 1;
SOMATOMEDIN BINDING PROTEIN 3;
ARTICLE;
CHROMOSOME 11;
CHROMOSOME 7;
CHROMOSOME 7P;
CLINICAL ARTICLE;
CONTROLLED STUDY;
GENE MUTATION;
GENOME;
GROWTH;
HUMAN;
HUMAN CELL;
LYMPHOCYTE;
PHENOTYPE;
PROTEIN EXPRESSION;
PUBERTY;
SILVER RUSSELL SYNDROME;
UNIPARENTAL DISOMY;
ABNORMALITIES, MULTIPLE;
ANEUPLOIDY;
ANIMALS;
CHROMOSOMES, HUMAN, PAIR 7;
CRANIOFACIAL ABNORMALITIES;
FATHERS;
GENE EXPRESSION REGULATION;
GENOMIC IMPRINTING;
GROWTH DISORDERS;
HUMANS;
INSULIN-LIKE GROWTH FACTOR BINDING PROTEIN 1;
INSULIN-LIKE GROWTH FACTOR BINDING PROTEIN 3;
MICE;
MOTHERS;
PHENOTYPE;
PROBABILITY;
SPECIES SPECIFICITY;
SYNDROME;
|
EID: 0032856646
PISSN: 00033995
EISSN: None
Source Type: Journal
DOI: None Document Type: Article |
Times cited : (13)
|
References (20)
|