| Consent for genetic research in a general population: The NHANES experience |
|
|
|
|
|
|
|
|
|
| Attitudes of African American premedical students toward genetic testing and screening |
|
|
|
|
|
|
|
|
|
| Announcements |
|
|
|
|
|
|
|
|
|
| Erratum |
|
|
|
|
|
|
|
|
|
| College News |
|
|
|
|
|
|
|
|
|
| Hereditary, familial, and idiopathic chronic pancreatitis are not associated with polymorphisms in the tumor necrosis factor α (TNF-α) promoter region or the TNF receptor 1 (TNFR1) gene |
|
|
|
|
|
|
|
|
|
| Early adoption of BRCA1/2 testing: Who and why |
|
|
|
|
|
|
|
|
|
| Fostering applications of genetics in primary care: What will it take? |
|
|
|
|
|
|
|
|
|
| Diffusion of innovations |
|
|
|
|
|
|
|
|
|
| Effects of pregnancy on the renal and pulmonary manifestations in women with tuberous sclerosis complex |
|
|
|
|
|
|
|
|
|
| Physicians’ perceived usefulness of and satisfaction with test reports for cystic fibrosis (ΔF508) and factor V Leiden |
|
|
|
|
|
|
|
|
|
| Update on HIPAA privacy: Are you ready? |
|
|
|
|
|
|
|
|
|
| Predictive genetics in primary care: Expectations for the motivational impact of genetic testing affects the importance family physicians place on screening for familial cancer risk |
|
|
|
|
|
|
|
|
|
| Direct-to-consumer sales of genetic services on the Internet |
|
|
|
|
|
|
|
|
|
| A survey of chairpersons of departments of medicine about the current and future roles of clinical genetics in internal medicine |
|
|
|
|
|
|
|
|
|
| Genetics and genomics in practice: The continuum from genetic disease to genetic information in health and disease |
|
|
|
|
|
|
|
|
|
| Early childhood hearing loss: Clinical and molecular genetics. An educational slide set of the American College of Medical Genetics |
|
|
|
|
|
|
|
|
|
| Frequency and distribution of GJB2 (connexin 26) and GJB6 (connexin 30) mutations in a large North American repository of deaf probands |
|
|
|
|
|
|
|
|
|
| Can mucopolysaccharidosis type I disease severity be predicted based on a patient’s genotype? A comprehensive review of the literature |
|
|
|
|
|
|
|
|
|
| Penetrance and expressivity in the molecular age |
|
|
|
|
|
|
|
|
|
| Fishing for a better language |
|
|
|
|
|
|
|
|
|
| Monitoring ethical, legal, and social issues in developing population genetic databases |
|
|
|
|
|
|
|
|
|
| Guidelines for breast and ovarian cancer genetic counseling referral: Adoption and implementation in HMOs |
|
|
|
|
|
|
|
|
|
| Genetics of hypertension |
|
|
|
|
|
|
|
|
|
| Hereditary hemochromatosis: Perspectives of public health, medical genetics, and primary care |
|
|
|
|
|
|
|
|
|
| Analytic validity of cystic fibrosis testing: A preliminary estimate |
|
|
|
|
|
|
|
|
|
| College News |
|
|
|
|
|
|
|
|
|
| Meetings Calendar |
|
|
|
|
|
|
|
|
|
| New Products |
|
|
|
|
|
|
|
|
|
| College news |
|
|
|
|
|
|
|
|
|
| New products |
|
|
|
|
|
|
|
|
|
| Erratum |
|
|
|
|
|
|
|
|
|
| Meetings Calendar |
|
|
|
|
|
|
|
|
|
| Attitudes of the broader hearing, deaf, and hard-of-hearing community toward genetic testing for deafness |
|
|
|
|
|
|
|
|
|
| Mutation spectrum of the connexin 26 (GJB2) gene in Taiwanese patients with prelingual deafness |
|
|
|
|
|
|
|
|
|
| Role of the geneticist in testing and counseling for inherited thrombophilia |
|
|
|
|
|
|
|
|
|
| It’s here… countdown to privacy under HIPAA |
|
|
|
|
|
|
|
|
|
| Comparative evaluation of α-galactosidase A infusions for treatment of Fabry disease |
|
|
|
|
|
|
|
|
|
| Williams syndrome deficits in visual spatial processing linked to GTF2IRD1 and GTF2I on Chromosome 7q11.23 |
|
|
|
|
|
|
|
|
|
| Proceedings of the Second International Conference on Neural Tube Defects |
|
|
|
|
|
|
|
|
|
| An economic viewpoint on alternative strategies for identifying persons with hereditary nonpolyposis colorectal cancer |
|
|
|
|
|
|
|
|
|
| Genetics and preventive medicine: Beyond family history |
|
|
|
|
|
|
|
|
|
| Attitudinal barriers to delivery of race-targeted pharmacogenomics among informed lay persons |
|
|
|
|
|
|
|
|
|
| Genomics and inductive reasoning: Revolution, renaissance, or rhetoric? |
|
|
|
|
|
|
|
|
|
| The Stickler syndrome: Genotype/phenotype correlation in 10 families with Stickler syndrome resulting from seven mutations in the type II collagen gene locus COL2A1 |
|
|
|
|
|
|
|
|
|
| Utility of subtelomeric fluorescent DNA probes for detection of chromosome anomalies in 425 patients |
|
|
|
|
|
|
|
|
|
| Teaching clinical management skills for genetic testing of hereditary nonpolyposis colorectal cancer using a Web-based tutorial |
|
|
|
|
|
|
|
|
|
| The genetics workforce and workload |
|
|
|
|
|
|
|
|
|
| Meetings Calendar |
|
|
|
|
|
|
|
|
|
| Meetings Calendar |
|
|
|
|
|
|
|
|
|
| Meetings Calendar |
|
|
|
|
|
|
|
|
|
| The genetic family history as a risk assessment tool in internal medicine |
|
|
|
|
|
|
|
|
|
| Barriers to the provision of genetic services by primary care physicians: A systematic review of the literature |
|
|
|
|
|
|
|
|
|
| Family history: Where to go from here |
|
|
|
|
|
|
|
|
|
| An argument of logic for the diagnosis of familial hypomobility |
|
|
|
|
|
|
|
|
|
| Postmortem findings in the Coffin-Lowry Syndrome |
|
|
|
|
|
|
|
|
|
| Determination and use of haplotypes: Ethnic comparison and association of the lipoprotein lipase gene and coronary artery disease in Mexican-Americans |
|
|
|
|
|
|
✓ |
|
Mexican-Americans |
| Genetic evaluation for coronary artery disease |
|
|
|
|
|
|
|
|
|
| Differences in physician referral practices and attitudes regarding hereditary breast cancer by clinical practice location |
|
|
|
|
|
|
|
|
|
| Screening for Fragile X Syndrome: Parent attitudes and perspectives |
|
|
|
|
|
|
|
|
|
| Response to Mikail |
|
|
|
|
|
|
|
|
|
| Informed lay preferences for delivery of racially varied pharmacogenomics |
|
|
|
|
|
|
|
|
|
| Prevalence of the C677T substitution of the methylenetetrahydrofolate reductase (MTHFR) gene in Wisconsin |
|
|
|
|
|
|
|
|
|
| Klinefelter syndrome: Expanding the phenotype and identifying new research directions |
|
|
|
|
|
|
|
|
|
| A founder COL17A1 splice site mutation leading to generalized atrophic benign epidermolysis bullosa in an extended inbred Palestinian family from Israel |
|
|
|
|
|
|
|
|
|
| Estimated analytic validity of HFE C282Y mutation testing in population screening: The potential value of confirmatory testing |
|
|
|
|
|
|
|
|
|
| Extensive sequencing of the cystic fibrosis transmembrane regulator gene: Assay validation and unexpected benefits of developing a comprehensive test |
|
|
|
|
|
|
|
|
|
| Prospective assessment in newborns of diabetes autoimmunity (PANDA): Maternal understanding of infant diabetes risk |
|
|
|
|
|
|
|
|
|
| Does knowledge about the genetics of breast cancer differ between nongeneticist physicians who do or do not discuss or order BRCA testing? |
|
|
|
|
|
|
|
|
|
| Lifeline: Helical and historical |
|
|
|
|
|
|
|
|
|
| Thrombocytopenia in patients with 22q11.2 deletion syndrome and its association with glycoprotein Ib-β |
|
|
|
|
|
|
|
|
|
| HFE genotype and transferrin saturation in the United States |
|
|
|
|
|
|
|
|
|
| As currently formulated, ISCN FISH nomenclature make it not practical for use in clinical test reports or cytogenetic databases |
|
|
|
|
|
|
|
|
|
| Is modern genetics the new eugenics? |
|
|
|
|
|
|
|
|
|
| Variability in clinical phenotype despite common chromosomal deletion in Smith-Magenis syndrome [del(17)(p11.2p11.2)] |
|
|
|
|
|
|
|
|
|
| Tetrahydrobiopterin control in phenylketonuria |
|
|
|
|
|
|
|
|
|
| Reviewer Acknowledgment |
|
|
|
|
|
|
|
|
|
| Meetings calendar |
|
|
|
|
|
|
|
|
|
| College News |
|
|
|
|
|
|
|
|
|
| New products |
|
|
|
|
|
|
|
|
|
| International genetic testing |
|
|
|
|
|
|
|
|
|
| Uncertainties in the molecular diagnosis of recessive hearing loss disorders |
|
|
|
|
|
|
|
|
|