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Mosaicism due to a Somatic Mutation of the Androgen Receptor Gene Determines Phenotype in Androgen Insensitivity Syndrome
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Holterhus, P.-M
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Issued for the Endocrine Society by the Williams & Wilkins Co
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1980
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2 |
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Cell Type-Specific Expression of 17�Hydroxysteroid Dehydrogenase Type 2in Human Placenta and Fetal Liver
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Moghrabi, N
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Issued for the Endocrine Society by the Williams & Wilkins Co
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1980
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3 |
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Urocortin Expression in Human Pituitary Gland and Pituitary Adenoma
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Iino, K
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Issued for the Endocrine Society by the Williams & Wilkins Co
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1980
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4 |
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Colocalization of 11�Hydroxysteroid Dehydrogenase Type II and Mineralocorticoid Receptor in Human Epithelia
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Hirasawa, G
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Issued for the Endocrine Society by the Williams & Wilkins Co
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1980
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5 |
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Germline Dinucleotide Mutation in Codon 883 of the Ret Proto-Oncogene inMultiple Endocrine Neoplasia Type 2B without Codon 918 Mutation
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Gimm, O
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Issued for the Endocrine Society by the Williams & Wilkins Co
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1980
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6 |
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Dexamethasone, OB Gene, and Leptin in Humans; Effect of Exogenous Hyperinsulinemia
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Kolaczynski, J. W
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Issued for the Endocrine Society by the Williams & Wilkins Co
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1980
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7 |
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Mild Clinical Expression of Myasthenia Gravis Associated with AutoimmuneThyroid Disease-Authors' Response
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Marino, M
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Issued for the Endocrine Society by the Williams & Wilkins Co
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1980
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8 |
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Premature Hair Graying and Bone Mineral Density
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Orr-Walker, B. J
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Issued for the Endocrine Society by the Williams & Wilkins Co
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1980
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9 |
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Somatic Mutations in the Thyrotropin Receptor Gene and Not in the G~s�Protein Gene in 31 Toxic Thyroid Nodules
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Fuehrer, D
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Issued for the Endocrine Society by the Williams & Wilkins Co
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1980
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10 |
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Substantial Production of Dopamine in the Human Gastrointestinal Tract
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Eisenhofer, G
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Issued for the Endocrine Society by the Williams & Wilkins Co
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1980
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