Isolated GH deficiency with dominant inheritance: New mutations, new insights

Journal of Clinical Endocrinology and Metabolism

Volumn 86, Issue 8, 2001, Pages 3877-3881

  Binder, G ^a   Keller, E ^b   Mix, M ^b   Massa, G G ^b   Stokvis Brantsma, W H ^b   Wit, J M ^b   Ranke, M B ^b  

^a UNIVERSITY HOSPITAL TÜBINGEN   (Germany)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

DNA; GROWTH HORMONE; PHENYLALANINE; RNA; SOMATOMEDIN; SOMATOMEDIN BINDING PROTEIN 3; VALINE;

ADENOHYPOPHYSIS; ARTICLE; BODY MASS; CATCH UP GROWTH; CHILD; CLINICAL ARTICLE; CONTROLLED STUDY; DISEASE SEVERITY; DNA SEQUENCE; DOMINANT INHERITANCE; EXON; FEMALE; GROWTH DISORDER; GROWTH HORMONE DEFICIENCY; HORMONE STRUCTURE; HUMAN; INTRON; LYMPHOCYTE; MALE; MISSENSE MUTATION; NUCLEAR MAGNETIC RESONANCE IMAGING; OBESITY; ORGAN SIZE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; RNA SPLICING;

EID: 0034880768     PISSN: 0021972X     EISSN: None     Source Type: Journal    
DOI: 10.1210/jcem.86.8.7757     Document Type: Article

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