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- A new association of congenital hydrocephalus, albinism, megalocornea, and retinal coloboma in a syndromic child: A clinical and genetic study Journal Articles
- 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 Journal Articles
- Analysis of IFT74as a candidate gene for chromosome 9p-linked ALS-FTD Journal Articles
- Association of Chromosome 9p21 With Subsequent Coronary Heart Disease Events Journal Articles
- Deletion 9q34.3 syndrome: genotype-phenotype correlations and an extended deletion in a patient with features of Opitz C trigonocephaly Journal Articles
- Disruption of the ASTN2/TRIM32 locus at 9q33.1 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypes Journal Articles
- Fluorescence <i>in Situ</i> Hybridization Studies on Breast Tumor Samples for Distinguishing Between Different Subsets of Breast Cancer Journal Articles
- Genome-Wide Association Meta-analysis of Neuropathologic Features of Alzheimer's Disease and Related Dementias Journal Articles
- Genome-wide association studies identify loci associated with age at menarche and age at natural menopause Journal Articles
- Modeling Complex Disease with Demographic and Environmental Covariates and a Candidate Gene Marker Journal Articles
- Predictive genetic testing for coronary artery disease Journal Articles
- The 9p21.3 locus and cardiovascular risk in familial hypercholesterolemia Journal Articles
- The Effect of Chromosome 9p21 Variants on Cardiovascular Disease May Be Modified by Dietary Intake: Evidence from a Case/Control and a Prospective Study Journal Articles
- Wolf-Hirschorn syndrome resulting from partial monosomy 4p/trisomy 9p Journal Articles