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- A new association of congenital hydrocephalus, albinism, megalocornea, and retinal coloboma in a syndromic child: A clinical and genetic study Academic Article
- Affected members of melanoma‐prone families with linkage to 9p21 but lacking mutations in CDKN2A do not harbor mutations in the coding regions of either CDKN2B or p19ARF Academic Article
- Analysis of IFT74as a candidate gene for chromosome 9p-linked ALS-FTD Academic Article
- Association of Chromosome 9p21 With Subsequent Coronary Heart Disease Events Academic Article
- Deletion 9q34.3 syndrome: genotype-phenotype correlations and an extended deletion in a patient with features of Opitz C trigonocephaly Academic Article
- Disruption of the ASTN2/TRIM32 locus at 9q33.1 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypes Academic Article
- Fluorescence <i>in Situ</i> Hybridization Studies on Breast Tumor Samples for Distinguishing Between Different Subsets of Breast Cancer Academic Article
- Genome-Wide Association Meta-analysis of Neuropathologic Features of Alzheimer's Disease and Related Dementias Academic Article
- Genome-wide association studies identify loci associated with age at menarche and age at natural menopause Academic Article
- Modeling Complex Disease with Demographic and Environmental Covariates and a Candidate Gene Marker Academic Article
- Predictive genetic testing for coronary artery disease Academic Article
- The 9p21.3 locus and cardiovascular risk in familial hypercholesterolemia Academic Article
- The Effect of Chromosome 9p21 Variants on Cardiovascular Disease May Be Modified by Dietary Intake: Evidence from a Case/Control and a Prospective Study Academic Article
- Wolf-Hirschorn syndrome resulting from partial monosomy 4p/trisomy 9p Academic Article