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Volumn 31, Issue 2, 2007, Pages 212-217
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Genetic diagnosis of multiple affected tissues in a patient with McCune-Albright syndrome
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Author keywords
Acromegaly; Gs gene; McCune Albright syndrome; Mutation
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Indexed keywords
ANTIINFLAMMATORY AGENT;
PROTEIN G;
PROTEIN G ALPHA;
TUBERCULOSTATIC AGENT;
UNCLASSIFIED DRUG;
STIMULATORY GUANINE NUCLEOTIDE BINDING PROTEIN;
ACROMEGALY;
ADULT;
ALBRIGHT SYNDROME;
ARTICLE;
BLOOD;
BONE TISSUE;
CAFE AU LAIT SPOT;
CASE REPORT;
CLINICAL ASSESSMENT;
CLINICAL FEATURE;
COMPUTER ASSISTED TOMOGRAPHY;
DNA ISOLATION;
ECHOGRAPHY;
GENE MUTATION;
GENE SEQUENCE;
GENETIC ANALYSIS;
GENETIC DISORDER;
HISTOPATHOLOGY;
HUMAN;
LABORATORY DIAGNOSIS;
MALE;
NUCLEAR MAGNETIC RESONANCE IMAGING;
PHYSICAL EXAMINATION;
PLEURA;
PLEURA EFFUSION;
POLYMERASE CHAIN REACTION;
PRIORITY JOURNAL;
RADIODIAGNOSIS;
SKIN DEFECT;
GENETICS;
MUTATION;
NUCLEOTIDE SEQUENCE;
PATHOLOGY;
TRANSPLANTATION;
ACROMEGALY;
ADULT;
BASE SEQUENCE;
CAFE-AU-LAIT SPOTS;
DNA MUTATIONAL ANALYSIS;
FIBROUS DYSPLASIA, POLYOSTOTIC;
GTP-BINDING PROTEIN ALPHA SUBUNITS, GS;
HUMANS;
MALE;
MUTATION;
TISSUE AND ORGAN HARVESTING;
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EID: 35348856333
PISSN: 1355008X
EISSN: 15590100
Source Type: Journal
DOI: 10.1007/s12020-007-0015-x Document Type: Article |
Times cited : (11)
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References (22)
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