Frequency of mutations in PROP-1 gene in Turkish children with combined pituitary hormone deficiency

Turkish Journal of Pediatrics

Volumn 54, Issue 6, 2012, Pages 570-575

  Kandemir, Nurgün ^a   Vuralli, Doǧuş ^a   Taşkiran, Ekim ^a   Gönç, Nazli ^a   Özön, Alev ^a   Alikaşifoǧlu, Ayfer ^a   Yilmaz, Engin ^a  

^a HACETTEPE UNIVERSITY   (Turkey)

Author keywords

Anterior pituitary; Growth hormone; Human; Hyposecretion syndrome; Paired like homeodomain transcription factor; Pituitary; Prophet of pit 1

Indexed keywords

GROWTH HORMONE; HYPOPHYSIS HORMONE; THYROTROPIN;

ADOLESCENT; ARTICLE; CHILD; CLINICAL FEATURE; COMBINED PITUITARY HORMONE DEFICIENCY; CONSANGUINITY; CONTROLLED STUDY; DNA POLYMORPHISM; ETHNIC GROUP; EXON; FEMALE; GENE; GENE MUTATION; GENETIC SCREENING; GROWTH HORMONE DEFICIENCY; HETEROZYGOSITY; HOMOZYGOSITY; HORMONE DEFICIENCY; HORMONE DETERMINATION; HUMAN; INFANT; MAJOR CLINICAL STUDY; MALE; MUTATION RATE; MUTATIONAL ANALYSIS; NUCLEAR MAGNETIC RESONANCE IMAGING; PREVALENCE; PROPHET OF PIT 1 GENE; SCHOOL CHILD; SEQUENCE ANALYSIS; THYROID STIMULATING HORMONE DEFICIENCY; TURKISH;

ADOLESCENT; CHILD; CHILD, PRESCHOOL; DNA; DNA MUTATIONAL ANALYSIS; FEMALE; GENE FREQUENCY; HETEROZYGOTE; HOMEODOMAIN PROTEINS; HUMANS; HYPOPITUITARISM; INFANT; MALE; MUTATION; PEDIGREE; PHENOTYPE; PREVALENCE; TRANSCRIPTION FACTORS; TURKEY;

EID: 84876090165     PISSN: 00414301     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (19)

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