A case of McCune-Albright syndrome associated with Gs alpha mutation in the bone tissue

Endocrine Journal

Volumn 53, Issue 1, 2006, Pages 35-44

  Sargin, Haluk ^a   Gozu, Hulya ^a,d   Bircan, Rifat ^b   Sargin, Mehmet ^a   Avsar, Melike ^b   Ekinci, Gazenfer ^b   Yayla, Ali ^a   Gulec, Ilker ^a   Bozbuga, Mustafa ^a   Cirakoglu, Beyazit ^b   Tanakol, Refik ^c  

^a Dr Lutfi Kirdar Kartal Research and Training Hospital   (Turkey)

^b MARMARA UNIVERSITY SCHOOL OF MEDICINE   (Turkey)

^c ISTANBUL UNIVERSITY   (Turkey)

^d Istanbul University Medical School ^*  (Turkey)

Author keywords

Acromegaly; Gs alpha mutation; McCune Albright Syndrome

Indexed keywords

ALENDRONIC ACID; GENOMIC DNA; OCTREOTIDE; SOMATOMEDIN C; SOMATOSTATIN DERIVATIVE;

ACROMEGALY; ADULT; ALBRIGHT SYNDROME; ANAMNESIS; ARTICLE; BONE TISSUE; CAFE AU LAIT SPOT; CASE REPORT; CLINICAL EXAMINATION; CLINICAL FEATURE; CRANIOFACIAL MORPHOLOGY; DNA ISOLATION; DNA SEQUENCE; GENE AMPLIFICATION; GENE MUTATION; HISTOPATHOLOGY; HUMAN; HYPERTHYROIDISM; HYPOPHYSIS TUMOR; LABORATORY TEST; LEUKOCYTE; MALE; NODULAR GOITER; PHYSICAL EXAMINATION; PRECOCIOUS PUBERTY;

ACROMEGALY; ARGININE; BONE AND BONES; CYSTEINE; DNA; DNA MUTATIONAL ANALYSIS; FACIAL BONES; FIBROUS DYSPLASIA, POLYOSTOTIC; GTP-BINDING PROTEIN ALPHA SUBUNITS, GS; HUMANS; HYPERTHYROIDISM; LEUKOCYTES; MALE; MIDDLE AGED; MUTATION; POLYMERASE CHAIN REACTION; SEQUENCE ANALYSIS, DNA; SKULL;

EID: 33645008434     PISSN: 09188959     EISSN: 13484540     Source Type: Journal    
DOI: 10.1507/endocrj.53.35     Document Type: Article

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