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Attention, chocolate lovers: You may not be able to help yourselves. Swiss and British scientists have linked the widespread love of chocolate to a chemical "signature" that may be programmed into our metabolic systems.
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Medical Reference
Genetic and Paternity Testing
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- ABO Blood Typing - Blood Typing
- Achondroplasia
- Achondroplastic Dwarfism - Achondroplasia
- Acute Myelogenous Leukemia - Acute Nonlymphocytic Leukemia
- Acute Nonlymphocytic Leukemia
- AML - Acute Nonlymphocytic Leukemia
- Anembryonic Pregnancy - Blighted Ovum
- Beta-Glucosidase Deficiency - Gaucher Disease
- Blighted Ovum
- Blood Typing
- Bronze Diabetes - Hemochromatosis
- Celiac Sprue - Celiac Disease
- Celiac Disease
- CF - Cystic Fibrosis
- Christmas Disease - Hemophilia B
- Complete Androgen Insensitivity Syndrome - Testicular Feminization
- Congenital Aganglionic Megacolon - Hirschsprung Disease
- Congenital Factor VIII Deficiency - Hemophilia A
- Craniosynostosis
- Cross Matching - Blood Typing
- Cystic Fibrosis
- DNA Testing
- Duchenne Muscular Dystrophy
- Enzymatic Disorders - Inborn Errors of Metabolism
- Factor IX Deficiency - Hemophilia B
- Familial Combined Hyperlipidemia
- Familial Hypercholesterolemia
- Familial Hypertriglyceridemia
- Gaucher Disease
- Genetic Counseling
- Genetic Screening
- Genetic Testing
- Gluten Intolerance - Celiac Disease
- Gluten-Sensitive Enteropathy - Celiac Disease
- GM2-Gangliosidosis, Type I - Tay-Sachs Disease
- Hemochromatosis
- Hemophilia A
- Hemophilia B
- Hepatolenticular Degeneration - Wilson's Disease
- Hereditary Hemochromatosis - Hemochromatosis
- Hexosaminidase A Deficiency - Tay-Sachs Disease
- Hirschsprung Disease
- Hunter Syndrome
- Huntington Chorea - Huntington Disease
- Huntington Disease
- Identity Testing
- Idiopathic Hemochromatosis - Hemochromatosis
- Inborn Errors of Metabolism
- Infantile Gaucher Disaese - Gaucher Disease
- Iron Overload Disease - Hemochromatosis
- Juvenile Gaucher Disease - Gaucher Disease
- Male Pseudohermaphroditism - Testicular Feminization
- Metabolic Disorders - Inborn Errors of Metabolism
- Mucopolysaccharidosis II - Hunter Syndrome
- Muscular Dystrophy
- Nontropical Sprue - Celiac Disease
- Parentage Testing - Identity Testing
- Paternity Testing - Identity Testing
- Phenylalanine Hydroxylase Deficiency - Phenylketonuria
- Phenylketonuria
- PKU - Phenylketonuria
- Preclinical Abortion - Blighted Ovum
- Pseudohypertrophic Muscular Dystrophy - Duchenne Muscular Dystrophy
- Rh Typing - Blood Typing
- Sprue - Celiac Disease
- Sulfo-Iduronate Sulfatase Deficiency - Hunter Syndrome
- Symptomatic Gastrinoma - Zollinger-Ellison Syndrome
- Tay-Sachs Disease
- Testicular Feminization
- Thyroid Cancer
- Type IIa Hyperlipoproteinemia - Familial Hypercholesterolemia
- Type IIb Hyperlipoproteinemia - Familial Combined Hyperlipidemia
- Type IV Hyperlipoproteinemia - Familial Hypertriglyceridemia
- Wilson's Disease
- Zollinger-Ellison Syndrome
Related Links
- GeneClinics: Medical Genetics Knowledge Base
- Genetic Assays Inc.
- GeneTests
- DNAprint Genomics inc.
- Genassist, Inc.
- Dynacare Northwest, Inc. Cytogenetics Laboratory
- Gene Dx
- The Gene Trust
- Interleukin Genetics Incorporated
- Gene Analysis Service GmbH
- The Robert Guthrie Biochemical Genetics Laboratory
- New York University Department of Pediatrics Human Genetics Program
- American Board of Genetic Counseling
- National Society of Genetic Counselers - NSGC
- Canadian Association of Genetic Counsellors - CAGC
- Kimball Genetics
- Human Gene Testing
- National Newborn Screening and Genetics Resource Center of the US
- Gendia - Genetic Diagnostics
- Gene Testing
- Molecular Genetics Testing Laboratory: Ashkenazi Jewish Genetic Disease Screen
- Gendia
- South East of Scotland Genetic Service
- Mountain States Genetics Network
- OHSU Genetic Service Laboratories