Monosomy 1p36 breakpoint junctions suggest pre-meiotic breakage–fusion–bridge cycles are involved in generating terminal deletions - Ballif, Blake C.; Yu, Wei; Shaw, Chad A.; Kashork, Catherine D.; Shaffer, Lisa G. (Human molecular genetics, 2003)
Keywords: Animals; Base Sequence; Biological and medical sciences; Cell Fusion; Chromosome aberrations; Chromosome Breakage; Chromosome Deletion; Chromosome Disorders - diagnosis; Chromosome Disorders - genetics; Chromosomes, Human, Pair 1 - genetics; Cricetinae; Cytogenetic Analysis; Diseases of the osteoarticular system; Gene Duplication; Humans; In Situ Hybridization, Fluorescence; Medical genetics; Medical sciences; Meiosis; Models, Genetic; Molecular Sequence Data; Monosomy - diagnosis; Monosomy - genetics; Nucleic Acid Hybridization; Repetitive Sequences, Nucleic Acid - genetics; Sequence Homology, Nucleic Acid; Telomere - genetics; Tumors of striated muscle and skeleton; Chromosomal aberration; Human; Breakpoint; Chromosome A1; Deletion; Aneuploidy; Mutation; Complex syndrome; Mental retardation; Terminal repeated sequence; Telomere; Monosomy