Searching for somatic mutations in McCune-Albright syndrome: A comparative study of the peptidic nucleic acid versus the nested PCR method based on 148 DNA samples

European Journal of Endocrinology

Volumn 155, Issue 6, 2006, Pages 839-843

  Kalfa, N ^a,b,c   Philibert, P ^a,b   Audran, F ^a,b   Ecochard, A ^a,b   Hannon, T ^d   Lumbroso, S ^a,b,c,e   Sultan, C ^a,b,c  

^a HÔPITAL ARNAUD DE VILLENEUVE   (France)

^b LAPEYRONIE HOSPITAL   (France)

^c INSERM   (France)

^d RILEY HOSPITAL FOR CHILDREN   (United States)

^e NÎMES UNIVERSITY HOSPITAL   (France)

Author keywords

[No Author keywords available]

Indexed keywords

DNA; NUCLEIC ACID;

ALBRIGHT SYNDROME; ARTICLE; BLOOD; BONE LESION; COMPARATIVE STUDY; CONTROLLED STUDY; DIAGNOSTIC ACCURACY; DIAGNOSTIC PROCEDURE; DNA SEQUENCE; HUMAN; HUMAN TISSUE; MAJOR CLINICAL STUDY; OVARY; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SOMATIC MUTATION; SYMPTOM; THERMOSTABILITY;

CHILD; DNA MUTATIONAL ANALYSIS; FEMALE; FIBROUS DYSPLASIA, POLYOSTOTIC; GENETIC SCREENING; GTP-BINDING PROTEIN ALPHA SUBUNITS, GS; HUMANS; MALE; PEPTIDE NUCLEIC ACIDS; POLYMERASE CHAIN REACTION; REPRODUCIBILITY OF RESULTS; RESTRICTION MAPPING; SENSITIVITY AND SPECIFICITY;

EID: 33845966717     PISSN: 08044643     EISSN: None     Source Type: Journal    
DOI: 10.1530/eje.1.02301     Document Type: Article

References (19)

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