subject area of
- ATM whole gene deletion in an Italian family with hereditary pancreatic cancer: Challenges to cancer risk prediction associated with an 11q22.3 microdeletion Journal Articles
- Aniridia--Wilms' tumour association--a case with 11p 13-14.1 deletion and ventricular septal defect. Journal Articles
- Association of breast cancer risk in BRCA1 and BRCA2 mutation carriers with genetic variants showing differential allelic expression: identification of a modifier of breast cancer risk at locus 11q22.3 Journal Articles
- Centrotemporal sharp wave EEG trait in rolandic epilepsy maps to Elongator Protein Complex 4 (ELP4) Journal Articles
- Chromosome-specific subsets of human alpha satellite DNA: Analysis of sequence divergence within and between chromosomal subsets and evidence for an ancestral pentameric repeat Journal Articles
- Cytogenetic Prognostication Within Medulloblastoma Subgroups Journal Articles
- De novo mutation of the DHCR7 gene in a fetus with severe Smith–Lemli–Opitz (or RSH) syndrome Journal Articles
- Detection of novel centromeric polymorphisms associated with alpha satellite DNA from human chromosome 11 Journal Articles
- Extraskeletal Ewing's Sarcoma/Primitive Neuroectodermal Tumor of the Posterior Mediastinum with t(11;22)(q24;q12) Journal Articles
- Fetal hemoglobin in sickle cell anemia: genome-wide association studies suggest a regulatory region in the 5′ olfactory receptor gene cluster Journal Articles
- Genome-wide Linkage Analyses of Quantitative and Categorical Autism Subphenotypes Journal Articles
- Genome-wide association and linkage identify modifier loci of lung disease severity in cystic fibrosis at 11p13 and 20q13.2 Journal Articles
- Hemoglobin Bart's Disease in an Italian Boy Journal Articles
- Identification of Genetic Loci Underlying the Phenotypic Constructs of Autism Spectrum Disorders Journal Articles
- Immunochip Analysis Identifies Multiple Susceptibility Loci for Systemic Sclerosis Journal Articles
- Mapping of the metalloproteinase gene matrilysin (MMP7) to human chromosome 11q21→q22 Journal Articles
- Organization and evolution of alpha satellite DNA from human chromosome 11 Journal Articles
- Pseudo-rearrangement of the MLL gene at chromosome 11q23: a cautionary note on genotype analysis of leukaemia patients Journal Articles
- Renal Cell Carcinoma With Xp 11.2 Translocation as a Second Tumor in a Long-Term Survivor of Advanced Neuroblastoma Journal Articles
- Severe presentation of Beckwith–Wiedemann syndrome associated with high levels of constitutional paternal uniparental disomy for chromosome 11p15 Journal Articles
- The Gene Encoding p120cas, a Novel Catenin, Localizes on Human Chromosome 11q11 (CTNND) and Mouse Chromosome 2 (Catns) Journal Articles
- The Ocular Manifestations of Jacobsen Syndrome: A Report of Four Cases and a Review of the Literature Journal Articles
- The T-cell receptor delta chain locus is disrupted in the T-ALL associated t(11;14)(p13;q11) translocation Journal Articles
- The genetics of hemoglobin A2 regulation in sickle cell anemia Journal Articles
- Using extended pedigrees to identify novel autism spectrum disorder (ASD) candidate genes Journal Articles