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Results 1 - 10 of 21 for Clinical investigation
  1. GNAT2 gene 
    ... FL, Zografos L, Abdelhak S, El Matri L. Clinical and genetic investigation of a large Tunisian family with complete achromatopsia: ...
    https://medlineplus.gov/genetics/gene/gnat2 - Genetics
  2. Mitochondrial trifunctional protein deficiency 
    ... Niida Y, Shigematsu Y, Iijima K, Yamaguchi S. Clinical and molecular investigation of 14 Japanese patients with complete TFP deficiency: ...
    https://medlineplus.gov/...hondrial-trifunctional-protein-deficiency - Genetics
  3. Primary macronodular adrenal hyperplasia 
    ... an armadillo repeat containing 5 (ARMC5) gene: a clinical and genetic investigation. J Clin Endocrinol Metab. 2014 Jun;99(6): ...
    https://medlineplus.gov/.../primary-macronodular-adrenal-hyperplasia - Genetics
  4. ARMC5 gene 
    ... an armadillo repeat containing 5 (ARMC5) gene: a clinical and genetic investigation. J Clin Endocrinol Metab. 2014 Jun;99(6): ...
    https://medlineplus.gov/genetics/gene/armc5 - Genetics
  5. DSPP gene 
    ... Malmgren B, Lindskog S, Elgadi A, Norgren S. Clinical, histopathologic, and genetic investigation in two large families with dentinogenesis imperfecta type ...
    https://medlineplus.gov/genetics/gene/dspp - Genetics
  6. Familial isolated hyperparathyroidism 
    ... V, De Caro R, Favia G, Palu G. Clinical, genetic, and histopathologic investigation of CDC73-related familial hyperparathyroidism. Endocr Relat Cancer. ...
    https://medlineplus.gov/.../familial-isolated-hyperparathyroidism - Genetics
  7. Hyperparathyroidism-jaw tumor syndrome 
    ... V, De Caro R, Favia G, Palu G. Clinical, genetic, and histopathologic investigation of CDC73-related familial hyperparathyroidism. Endocr Relat Cancer. ...
    https://medlineplus.gov/.../hyperparathyroidism-jaw-tumor-syndrome - Genetics
  8. CDC73 gene 
    ... V, De Caro R, Favia G, Palu G. Clinical, genetic, and histopathologic investigation of CDC73-related familial hyperparathyroidism. Endocr Relat Cancer. ...
    https://medlineplus.gov/genetics/gene/cdc73 - Genetics
  9. Dentinogenesis imperfecta 
    ... Malmgren B, Lindskog S, Elgadi A, Norgren S. Clinical, histopathologic, and genetic investigation in two large families with dentinogenesis imperfecta type ...
    https://medlineplus.gov/genetics/condition/dentinogenesis-imperfecta - Genetics
  10. Apert syndrome 
    ... A, Gos M, Obersztyn E. Craniosynostosis as a clinical and diagnostic problem: ... a histological investigation. Orthod Craniofac Res. 2010 Feb;13(1):61- ...
    https://medlineplus.gov/genetics/condition/apert-syndrome - Genetics
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