Genetics of scleroderma

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A study of 27 patients, Biomedicine, 16, 648 Pan, 1975, Chromosomal abnormalities in progressive systemic sclerosis (scleroderma) with consideration of radiation effects, J Lab Clin Med, 300 Emerit, 1973, Sclérodermie generalísee et cassures chromosomiques. Mise en evidence d'un “facteur cassant” dans la serum des malades, Ann Genet, 135 Wolff, 1991, Spontaneous and clastogen induced chromosomal breakage in scleroderma, J Rheumatol, 18, 837 Emerit, 1976, Chromosomal breakage and scleroderma. 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An inherited human disease involving radiosensitivity, malignancy and defective DNA repair, 207 Emerit, 1976, Chromosomal breakage in systemic sclerosis and related disorders, Dermatologica, 153, 145, 10.1159/000251109 Tsay, 1992, Chromosome studies in systemic sclerosis with consideration of antibodies to topoisomerase I, Ann Rheum Dis, 51, 624, 10.1136/ard.51.5.624 Haaft Schmid, 1988, Analysis of double minutes and double minute-like chromatin in human and murine tumour cells using antikinetochore antibodies, Cancer Genet Cytogenet, 30, 73, 10.1016/0165-4608(88)90094-5 Haaft Summer, 1992, A micro-chromosome derived from chromosome 11 in a patient with the CREST syndrome of scleroderma, Cytogenet Cell Genet, 60, 12, 10.1159/000133284