66 Conventional detection of somatic GNAS1 mutation utilizing peripheral blood leukocyte in McCune-Albright syndrome
スポンサーリンク
概要
著者
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Kinoshita E
Department Of Pediatrics Nagasaki University School Of Medicine
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Motomura K
Department Of Pediatrics Nagasaki University Graduate School Of Biomedical Sciences
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Yoshimoto M
Children's Clinic Yoshimoto
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Yoshimoto M
Children's Clinic Yoshimoto
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Kinoshita E
Department Of Pediatrics Nagasaki University Graduate School Of Biomedical Sciences
関連論文
- 243 A CASE OF McCUNE-ALBRIGHT SYNDROME WITH NARROWING OPTIC CANAL : A TRIAL OF INTRAVENOUS PAMIDRONATE TREATMENT
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- 40 A NOVEL MUTATION OF 25-HYDROXY VITAMIN D3 1α-HYDROXYLASE GENE IN A JAPANESE FAMILY WITH VITAMIN D DEPENDENT RICKETS TYPE1
- 53 PITUITARY MAGNETIC RESONANCE IMAGING IN CHILDREN WITH GROWTH HORMONE DEFICIENCY
- 66 Conventional detection of somatic GNAS1 mutation utilizing peripheral blood leukocyte in McCune-Albright syndrome
- 64 GNAS1 mutation in a Japanese boy with progressive osseous heteroplasia.
- 98 A male-raised 46, XX case of congenital adrenal hyperplasia due to 21 hydroxylase deficiency
- 101 A female case of classical 3β-hydroxysteroid dehydrogenase deficiency with multicystic ovary and anovulatory menstruation : Evaluation of ovarian function after puberty
- 109 A case of allergy to gelatin included in the gonadotropin-releasing hormone analog "depot leuprorelin acetate"
- 83 Analysis of suppressor of cytokine signaling-2 (SOCS-2) gene in overgrowth syndrome