| Genetic diseases of the skin: Progress and perspectives |
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| The genetics of skin cancer |
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| Gene therapy and the skin |
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| Gap junction diseases of the skin |
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| Ectodermal dysplasias |
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| Calcium pump disorders of the skin |
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| Molecular genetics of hereditary hair and nail disease |
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| Progress in epidermolysis bullosa: Genetic classification and clinical implications |
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| The keratins and their disorders |
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| Molecular genetics of the ichthyoses |
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| Genetics of pigmentary disorders |
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| Inherited cancer predisposition |
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| Genetic conditions associated with intestinal juvenile polyps |
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| Genetic insights into familial tumors of the nervous system |
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| Simple and complex genetics of colorectal cancer susceptibility |
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Ashkenazi |
| Inherited predisposition to cancer: A historical overview |
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| Unravelling the genetics of prostate cancer |
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| Genomic imprinting and environment in hereditary paraganglioma |
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| Loss of DNA mismatch repair function and cancer predisposition in the mouse: Animal models for human hereditary nonpolyposis colorectal cancer |
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| Retinoblastoma: Revisiting the model prototype of inherited cancer |
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| Familial Wilms tumor |
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| Breast cancer genetics: Unsolved questions and open perspectives in an expanding clinical practice |
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| Cost of fetal alcohol spectrum disorders |
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| Alcohol consumption and other maternal risk factors for fetal alcohol syndrome among three distinct samples of women before, during, and after pregnancy: The risk is relative |
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| Fetal alcohol syndrome |
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| Monitoring prenatal alcohol exposure |
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| Fetal, infant, and child mortality in a context of alcohol use |
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| Recognition of facial features of fetal alcohol syndrome in the newborn |
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Black ancestry |
| An analysis of the effects of prenatal alcohol exposure on growth: A teratologic model |
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| Teratogenic effects of alcohol: A decade of brain imaging |
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| Epidemiologic approaches to identifying environmental causes of birth defects |
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| Integration of new genetic diseases into statewide newborn screening: New England experience |
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| Methodology of a multistate study of congenital hearing loss: Preliminary data from Utah newborn screening |
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| Public health approach to birth defects, developmental disabilities, and genetic conditions |
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| Vitamin supplements and the risk for congenital anomalies other than neural tube defects |
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| Ethical issues concerning genetic testing and screening in public health |
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| Public health monitoring of developmental disabilities with a focus on the autism spectrum disorders |
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| Utility and limitations of genetic disease databases in clinical genetics research: A neurofibromatosis 1 database example |
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| Contribution of Mendelian disorders to common chronic disease: Opportunities for recognition, intervention, and prevention |
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