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Follow-up findings in a Turkish girl with pseudohypoparathyroidism type ia caused by a novel heterozygous mutation in the GNAS gene
Sezgin Şahin,
Olaf Hiort
, Susanne Thiele, Olcay Evliyaoğlu, Beyhan Tüysüz
*
*
Corresponding author for this work
Clinic of Pediatric and Adolescent Medicine
Istanbul University, Cerrahpasa Faculty of Medicine
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Medicine and Dentistry
Pseudohypoparathyroidism
100%
Albright's Hereditary Osteodystrophy
75%
Growth Hormone
50%
Short Stature
50%
Hormone Determination
25%
Clinical Finding
25%
Isotopes of Calcium
25%
Thyrotropin
25%
Brachydactyly
25%
Heterotopic Ossification
25%
Gene Mutation
25%
Parathyroid Hormone
25%
Hormone Resistance
25%
Biochemistry, Genetics and Molecular Biology
Bovine Somatotropin
100%
Gene Mutation
50%
Hormone Resistance
50%
Parathyroid Hormone
50%
Calcium Blood Level
50%
Phosphate Blood Level
50%
Thyroid-Stimulating Hormone
50%