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- A RARE CASE OF INTERSTITIAL del(1)(p34.3p36.11) DIAGNOSED PRENATALLY Journal Articles
- Acute Lymphoblastic Leukemia in a Patient With Constitutional Chromosome 1pter-p36.31 Duplication and 1q43-qter Deletion Journal Articles
- Alterations in chromosome 1q in multiple myeloma randomized clinical trials: a systematic review Journal Articles
- Association of genomic subtypes of lower-grade gliomas with shape features automatically extracted by a deep learning algorithm Journal Articles
- Characterization of a highly polymorphic trinucleotide short tandem repeat within the human antithrombin gene Journal Articles
- Chromosome-specific alpha satellite DNA from human chromosome 1: Hierarchical structure and genomic organization of a polymorphic domain spanning several hundred kilobase pairs of centromeric DNA 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
- De novo 1q32q44 duplication and distal 1q trisomy syndrome Journal Articles
- Duplication of AKT3 as a cause of macrocephaly in duplication 1q43q44 Journal Articles
- Fluorescence <i>in Situ</i> Hybridization Studies on Breast Tumor Samples for Distinguishing Between Different Subsets of Breast Cancer Journal Articles
- Further evidence that a 100 Kb critical region is responsible for developmental delay, seizures, and dysmorphic features in 1q43q44 deletion patients Journal Articles
- Genetic Analysis of 103 Candidate Genes for Coronary Artery Disease and Associated Phenotypes in a Founder Population Reveals a New Association between Endothelin-1 and High-Density Lipoprotein Cholesterol Journal Articles
- Genetic interaction between α4 and β2 subunits of high affinity nicotinic receptor: analysis in schizophrenia Journal Articles
- Meta-genome-wide association studies identify a locus on chromosome 1 and multiple variants in the MHC region for serum C-peptide in type 1 diabetes Journal Articles
- Molecular Analysis of Phyllodes Tumors Reveals Distinct Changes in the Epithelial and Stromal Components Journal Articles
- Monosomy 3pter-p25.3 and Trisomy 1q42.13-qter in a Boy With Profound Growth and Developmental Restriction, Multiple Congenital Anomalies, and Early Death Journal Articles
- Partial monosomy 1q43 and partial trisomy 20q13.2: a case report Journal Articles
- SPEN haploinsufficiency causes a neurodevelopmental disorder overlapping proximal 1p36 deletion syndrome with an episignature of X chromosomes in females Journal Articles
- ‘Putting our heads together’: insights into genomic conservation between human and canine intracranial tumors Journal Articles