Contents
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Requires Authentication UnlicensedCONTENTSLicensedJuly 1, 2000
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Requires Authentication UnlicensedLetter from the EditorsLicensedJuly 1, 2000
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Requires Authentication UnlicensedPrader-Willi and Angelman Syndromes: Diagnostic ApproachLicensedJuly 1, 2000
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Requires Authentication UnlicensedArgl83His, a New Mutational "Hot-Spot" in the Growth Hormone GeneLicensedJuly 1, 2000
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Requires Authentication UnlicensedNovel Mutation (Arg836ter) of the Sulfonylurea Receptor-1 (SUR1) Gene in Congenital HyperinsulinismLicensedJuly 1, 2000
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Requires Authentication UnlicensedDe novo RET Mutation Positive Multiple Endocrine Neoplasia Type 2B and Hereditary Nonpolyposis Colorectal Cancer Syndrome Occurring in the Same Family: Parent-of-Origin and Mismatch RepairLicensedJuly 1, 2000
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Requires Authentication UnlicensedBromocriptine Resistant Prolactinomas and Non-Functioning Pituitary Tumors: Somatic Mutational Analyses of the Dopamine Type 2 Receptor and the MEN1 GeneLicensedJuly 1, 2000
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Requires Authentication UnlicensedGenetic Studies in Familial Aldosteronism Not Suppressible by DexamethasoneLicensedJuly 1, 2000
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Requires Authentication UnlicensedRecombination Between the Sodium Channel SCN8A and the Allgrove Syndrome Gene in a Puerto Rican KindredLicensedJuly 1, 2000
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Requires Authentication UnlicensedBOOK REVIEWS. CALENDARLicensedJuly 1, 2000