American Journal of Medical Genetics Part C: Seminars in Medical Genetics - 2004

39 articles | Last updated: 2025-12-03 14:12:55
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T A T A T A T A
Genetic diseases of the skin: Progress and perspectives
The genetics of skin cancer
Gene therapy and the skin
Gap junction diseases of the skin
Ectodermal dysplasias
Calcium pump disorders of the skin
Molecular genetics of hereditary hair and nail disease
Progress in epidermolysis bullosa: Genetic classification and clinical implications
The keratins and their disorders
Molecular genetics of the ichthyoses
Genetics of pigmentary disorders
Inherited cancer predisposition
Genetic conditions associated with intestinal juvenile polyps
Genetic insights into familial tumors of the nervous system
Simple and complex genetics of colorectal cancer susceptibility Ashkenazi
Inherited predisposition to cancer: A historical overview
Unravelling the genetics of prostate cancer
Genomic imprinting and environment in hereditary paraganglioma
Loss of DNA mismatch repair function and cancer predisposition in the mouse: Animal models for human hereditary nonpolyposis colorectal cancer
Retinoblastoma: Revisiting the model prototype of inherited cancer
Familial Wilms tumor
Breast cancer genetics: Unsolved questions and open perspectives in an expanding clinical practice
Cost of fetal alcohol spectrum disorders
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
Fetal alcohol syndrome
Monitoring prenatal alcohol exposure
Fetal, infant, and child mortality in a context of alcohol use
Recognition of facial features of fetal alcohol syndrome in the newborn Black ancestry
An analysis of the effects of prenatal alcohol exposure on growth: A teratologic model
Teratogenic effects of alcohol: A decade of brain imaging
Epidemiologic approaches to identifying environmental causes of birth defects
Integration of new genetic diseases into statewide newborn screening: New England experience
Methodology of a multistate study of congenital hearing loss: Preliminary data from Utah newborn screening
Public health approach to birth defects, developmental disabilities, and genetic conditions
Vitamin supplements and the risk for congenital anomalies other than neural tube defects
Ethical issues concerning genetic testing and screening in public health
Public health monitoring of developmental disabilities with a focus on the autism spectrum disorders
Utility and limitations of genetic disease databases in clinical genetics research: A neurofibromatosis 1 database example
Contribution of Mendelian disorders to common chronic disease: Opportunities for recognition, intervention, and prevention