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Borgaonkar DS. Chromosomal Variation in Man: A Catalog of Chromosomal Variants and Anomalies: Online NLM Version [Internet]. Bethesda (MD): National Center for Biotechnology Information (US); 1975-.
Chromosomal Variation in Man: A Catalog of Chromosomal Variants and Anomalies: Online NLM Version [Internet].
Show details- Emerit I: Chromosomal breakage in systemic sclerosis and related disorders. Dermatologica 153:145-156, 1976. [PubMed: 14037]
Emerit I, Housset E: Chromosome studies on bone marrow from patients with systemic sclerosis. Evidence for chromosomal breakage in vivo. Biomedicine 19:550-554, 1973.
Emerit I, Housset E, Feingold J: Chromosomal breakage and scleroderma: studies in family members. J. Lab. Clin. Med. 88:81-86, 1976. [PubMed: 932535]
Emerit I, Levy A, Housset E: Chromosomal breakage in scleroderma. Possible presence of a breakage factor in the serum of patients. Ann. Genet. 16:135-138, 1973. [PubMed: 4541907]
Emerit I, Levy A, Housset E: Breakage factor in systemic sclerosis and protector effect of L-cysteine. Humangenetik 25:221-226, 1974. [PubMed: 4448453] - Huet-Warembourg E, Legoff D, Jalbert H, Sele B, Amblard P, Reymoud J L, Jalbert P, Pison H: Cytogenetic aspects of diffuse scleroderma: structural anomalies and sister chromatid exchanges. Ann. Genet. 25:32-35, 1982. [PubMed: 6979297]
- Pan S F, Rodman G P, Deutsch M, Wald N: Chromosomal abnormalities in progressive systemic sclerosis (scleroderma) with consideration of radiation effects. J. Lab. Clin. Med. 86:300-308, 1975. [PubMed: 1151153]Sixty-three patients were found to have an increased frequency of cytogenetic aberrations. It appears that in PSS patients the increased chromosomal breakage is not associated with an elevated frequency of leukemia or other neoplasms.Index Terms: Leukemia
- Schmid M, Haaf T, Schindler D, Meurer M: Centromeric association of a microchromosome. A new category of non-random arrangement of metaphase chromosomes. Hum. Genet. 81:127-136, 1989. [PubMed: 2912883]
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