Genetic screening of combined pituitary hormone deficiency: Experience in 195 patients

Journal of Clinical Endocrinology and Metabolism

Volumn 91, Issue 9, 2006, Pages 3329-3336

  Reynaud, Rachel ^a,c   Gueydan, Magali ^a   Saveanu, Alexandru ^a,b,c   Vallette Kasic, Sophie ^a   Enjalbert, Alain ^b,c   Brue, Thierry ^a,c   Barlier, Anne ^a,b,c  

^a TIMONE HOSPITAL   (France)

^b HÔPITAL DE LA CONCEPTION   (France)

^c CNRS   (France)

Author keywords

[No Author keywords available]

Indexed keywords

GROWTH HORMONE; HOMEODOMAIN PROTEIN; HYPOPHYSIS HORMONE; LIM PROTEIN; THYROTROPIN;

ARTICLE; BRAIN MALFORMATION; CONTROLLED STUDY; FAMILY HISTORY; FEMALE; GENE MUTATION; GENETIC DISORDER; GENETIC SCREENING; HEREDITY; HORMONE DEFICIENCY; HUMAN; INFUNDIBULUM; MAJOR CLINICAL STUDY; MALE; NUCLEOTIDE SEQUENCE; PHENOTYPE; PREVALENCE; PRIORITY JOURNAL; RECURRENCE RISK;

EID: 33748745395     PISSN: 0021972X     EISSN: 0021972X     Source Type: Journal    
DOI: 10.1210/jc.2005-2173     Document Type: Article

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