IGF-I Receptor Mutations and Intrauterine and Postnatal Growth Retardation [4] (multiple letters)

New England Journal of Medicine

Volumn 350, Issue 13, 2004, Pages 1362-1363

  Unger, Sheila ^a   Chernausek, Steven D ^b   Kiess, Wieland ^c   Smith, Robert J ^d  

^a HOSPITAL FOR SICK CHILDREN   (Canada)

^b CINCINNATI CHILDREN'S HOSPITAL MEDICAL CENTER   (United States)

^c Hosp for Children and Adolescents   (Germany)

^d Hallett Center for Diabetes and Endocrinology   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

SOMATOMEDIN C RECEPTOR;

AMINO ACID SUBSTITUTION; BINDING KINETICS; CLINICAL FEATURE; GENE MUTATION; GENE SEQUENCE; GENETIC CODE; GROWTH RETARDATION; HETEROZYGOSITY; HUMAN; INTRAUTERINE GROWTH RETARDATION; LETTER; MISSENSE MUTATION; NONHUMAN; NONSENSE MUTATION; PRIORITY JOURNAL; PROTEIN BINDING; PROTEIN BLOOD LEVEL; PROTEIN PHOSPHORYLATION; SEQUENCE ANALYSIS;

ANIMALS; CHILD, PRESCHOOL; CODON, NONSENSE; DEVELOPMENTAL DISABILITIES; GROWTH DISORDERS; HUMANS; INSULIN-LIKE GROWTH FACTOR I; MICE; MICE, KNOCKOUT; MUTATION, MISSENSE; RECEPTOR, IGF TYPE 1; SYNDROME;

EID: 1642319683     PISSN: 00284793     EISSN: None     Source Type: Journal    
DOI: 10.1056/NEJMc040020     Document Type: Letter

References (0)