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Hetal Shah, Caterina Pipino, Sabrina Prudente, Natalia Di Pietro, Lixia Zeng, Kyoungmin Park, Vincenzo Trischitta, Subramanian Pennathur, Assunta Pandolfi, Alessandro Doria

Diabetes 2021;69(10):2206-2216

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A case of myelodysplastic syndrome with acquired monosomy 7 in a child with a constitutional t(1;19) and a mosaicism for trisomy 21.

Urvashi Surti, Jie Hu, Sofia Shekhter-Levin, Peter H Shaw, Carolyn Bay, Sally Kochmar

Cancer genetics and cytogenetics 2005;156(1):62-7

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Results for ""Chromosomes, Human, Pair 1""[mesh_terms]

Identification of a minimal region of loss on the short arm of chromosome 1 in Wilms tumor.

Red cell pyruvate kinase deficiency: from genetics to clinical manifestations.

Molecular basis of the Duffy blood group system.

Familial partial lipodystrophy: a monogenic form of the insulin resistance syndrome.

Glutathione S-transferase polymorphisms and colorectal cancer: a HuGE review.

Role of phosphoinositide-specific phospholipase C η2 in isolated and syndromic mental retardation.

Anti-CD38 monoclonal antibodies in multiple myeloma with gain/amplification of chromosome arm 1q: a review of the literature.

Atrial natriuretic peptide prohormone gene expression: hormones and diseases that upregulate its expression.

Clinical report of a pure subtelomeric 1qter deletion in a boy with mental retardation and multiple anomalies adds further evidence for a specific phenotype.

The Association between Serum LDL Cholesterol and Genetic Variation in Chromosomal Locus 1p13.3 among Coronary Artery Disease Patients.

Phenotypes of AKT3 deletion: a case report and literature review.

Genes, exercise and sudden death: molecular basis of familial catecholaminergic polymorphic ventricular tachycardia.

The multifunctional S100 protein family.

Association of the 1q25 Diabetes-Specific Coronary Heart Disease Locus With Alterations of the γ-Glutamyl Cycle and Increased Methylglyoxal Levels in Endothelial Cells.

A case of myelodysplastic syndrome with acquired monosomy 7 in a child with a constitutional t(1;19) and a mosaicism for trisomy 21.

Results for
""Chromosomes, Human, Pair 1""[mesh_terms]