Annals of Human Genetics · 1987 · 22 citations · 31 references
Life SciencesGeneticsMolecular GeneticsCytogeneticsGenome OrganizationHuman GeneticsChromosomal TranslocationsChromosome MappingGene MappingMolecular CytogeneticsStructural Chromosome AbnormalitiesX-chromosome InactivationComplex Chromosome RearrangementsFamilial Inheritance PatternsMendelian Inheritance PatternsPhysical Genome MappingPseudoautosomal InheritancePseudoautosomal Region AlterationsSomatic Chromosomal TranslocationsX Chromosome Structure
Human-rodent somatic cell hybrids containing deleted and translocated human X chromosomes have been used to map genes and sequences in and around the pseudoautosomal region. The following order was found: (DXS69, DXS70, DXS143)-(DXS31, STS)-MIC2. This order is consistent with the known inheritance patterns of DXS31, STS and MIC2. Assuming that the translocations and deletions we have studied are not complex rearrangements, we conclude that the pseudoautosomal region consists of less than 5 X 10(6) bp of DNA.
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P. S Harper · Journal of Medical Genetics · 1987 · 581 citations · Full text
A strategy to reveal high-frequency RFLPs along the human X chromosome.
Julie Aldridge, Louis M. Kunkel, G.A.P. Bruns et al. · PubMed · 1984 · 366 citations