{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,12,20]],"date-time":"2025-12-20T21:37:59Z","timestamp":1766266679761},"reference-count":18,"publisher":"Springer Science and Business Media LLC","issue":"3","license":[{"start":{"date-parts":[[1980,9,1]],"date-time":"1980-09-01T00:00:00Z","timestamp":336614400000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/www.springer.com\/tdm"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Hum Genet"],"published-print":{"date-parts":[[1980,9]]},"DOI":"10.1007\/bf00290214","type":"journal-article","created":{"date-parts":[[2004,10,5]],"date-time":"2004-10-05T05:53:21Z","timestamp":1096955601000},"page":"337-340","source":"Crossref","is-referenced-by-count":11,"title":["A case of pure red cell aplasia with a high incidence of spontaneous chromosome breakage: A possible X-ray sensitive syndrome"],"prefix":"10.1007","volume":"55","author":[{"given":"O.","family":"Iskandar","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"M. J.","family":"Jager","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"R.","family":"Willenze","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"A. T.","family":"Natarajan","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"297","reference":[{"key":"CR1","doi-asserted-by":"crossref","first-page":"8","DOI":"10.1056\/NEJM196601062740102","volume":"274","author":"GE Bloom","year":"1966","unstructured":"Bloom GE, Warner S, Park SG, Diamond LK (1966) Chromosome abnormalities in constitutional aplastic anemia. N Engl J Med 274:8?14","journal-title":"N Engl J Med"},{"key":"CR2","doi-asserted-by":"crossref","first-page":"4508","DOI":"10.1073\/pnas.71.11.4508","volume":"71","author":"RSK Chaganti","year":"1974","unstructured":"Chaganti RSK, Schonberg S, German J (1974) A manyfold increase in sister chromatid exchanges in Bloom's syndrome lymphocytes. Proc Natl Acad Sci USA 71:4508?4512","journal-title":"Proc Natl Acad Sci USA"},{"key":"CR3","doi-asserted-by":"crossref","first-page":"321","DOI":"10.1016\/0027-5107(76)90105-6","volume":"41","author":"PI Countryman","year":"1976","unstructured":"Countryman PI, Heddle JA (1976) The production of micronuclei from chromosome aberrations in irradiated cultures of human lymphocytes. Mutat Res 41:321?332","journal-title":"Mutat Res"},{"key":"CR4","first-page":"233","volume":"4","author":"G Fanconi","year":"1967","unstructured":"Fanconi G (1967) Familial Constitutional Panmyelopathy, Fanconi's Anemia (F.A.). I. Clinical aspects. Seminars in Hematology 4:233?240","journal-title":"Seminars in Hematology"},{"key":"CR5","first-page":"2983","volume":"38","author":"JA Heddle","year":"1978","unstructured":"Heddle JA, Lue CB, Saunders EF, Benz RD (1978) Sensitivity to five mutagens in Fanconi's Anemia as measured by the micronucleus test. Cancer Res 38:2983?2988","journal-title":"Cancer Res"},{"key":"CR6","doi-asserted-by":"crossref","first-page":"336","DOI":"10.1182\/blood.V38.3.336.336","volume":"38","author":"M Higurashi","year":"1971","unstructured":"Higurashi M, Conen PE (1971) In vitro chromosomal radiosensitivity in Fanconi's Anemia. Blood 38:336?342","journal-title":"Blood"},{"key":"CR7","doi-asserted-by":"crossref","first-page":"380","DOI":"10.1002\/1097-0142(197308)32:2<380::AID-CNCR2820320214>3.0.CO;2-2","volume":"32","author":"M Higurashi","year":"1973","unstructured":"Higurashi M, Conen PE (1973) In vitro chromosomal radiosensitivity in ?chromosomal breakage syndromes. Cancer 32:380?383","journal-title":"Cancer"},{"key":"CR8","first-page":"221","volume":"54","author":"O Iskandar","year":"1979","unstructured":"Iskandar O (1979) An improved method for the detection of micronuclei in human lymphocytes. Stain Technology 54: 221?223","journal-title":"Stain Technology"},{"key":"CR9","first-page":"418","volume-title":"Mendelian inheritance in man","author":"VA McKusick","year":"1978","unstructured":"McKusick VA (1978) Mendelian inheritance in man, 5th edn. Johns Hopkins University Press, Baltimore London, pp 418?419","edition":"5th edn."},{"key":"CR10","first-page":"139","volume":"95","author":"AT Natarajan","year":"1976","unstructured":"Natarajan AT (1976) Molecular aspects of the origin of chromosome structural changes. Biol Zentralbl 95:139?156","journal-title":"Biol Zentralbl"},{"key":"CR11","doi-asserted-by":"crossref","first-page":"127","DOI":"10.1007\/BF00284606","volume":"52","author":"AT Natarajan","year":"1979","unstructured":"Natarajan AT, Meyers M (1979) Chromosomal radiosensitivity of Ataxia telangiectasia cells at different cell cycle stages. Hum Genet 52:127?132","journal-title":"Hum Genet"},{"key":"CR12","doi-asserted-by":"crossref","first-page":"489","DOI":"10.1172\/JCI108960","volume":"6","author":"DG Nathan","year":"1978","unstructured":"Nathan DG, Clarke BJ, Hillman DG, Alter BP, Housman DE (1978) Erythroid precursors in congenital hypoplastic (Diamond-Blackfan) anemia. J Clin Invest 6:489?498","journal-title":"J Clin Invest"},{"key":"CR13","doi-asserted-by":"crossref","first-page":"121","DOI":"10.1038\/258121a0","volume":"258","author":"P Perry","year":"1975","unstructured":"Perry P, Evans HJ (1975) Cytological detection of mutagencarcinogen exposure by sister chromatid exchanges. Nature 258:121?125","journal-title":"Nature"},{"key":"CR14","doi-asserted-by":"crossref","first-page":"156","DOI":"10.1038\/251156a0","volume":"251","author":"P Perry","year":"1974","unstructured":"Perry P, Wolff S (1974) New Giemsa method for the differential staining of sister chromatids. Nature 251:156?158","journal-title":"Nature"},{"key":"CR15","first-page":"1829","volume":"33","author":"MS Sasaki","year":"1973","unstructured":"Sasaki MS, Tonomura A (1973) A high susceptibility of Fanconi's anemia to chromosome breakage by DNA cross linking agents. Cancer Res 33:1829?1836","journal-title":"Cancer Res"},{"key":"CR16","first-page":"241","volume":"4","author":"W Schmid","year":"1967","unstructured":"Schmid W (1967) Familial Constitutional Panmyelopathy, Fanconi's Anemia (F.A.). II. A discussion of the cytogenetic findings in Fanconi's Anemia. Seminars in Hematology 4: 241?249","journal-title":"Seminars in Hematology"},{"key":"CR17","doi-asserted-by":"crossref","first-page":"990","DOI":"10.1016\/0002-9343(66)90056-8","volume":"41","author":"AP Tartaglia","year":"1966","unstructured":"Tartaglia AP, Propp S, Amarose AP, Propp RP, Hall CA (1966) Chromosome abnormality and hypocalcemia in congenital erythroid hypoplasia (Blackfan-Diamond Syndrome). Am J Med 41:990?999","journal-title":"Am J Med"},{"key":"CR18","doi-asserted-by":"crossref","first-page":"427","DOI":"10.1038\/258427a0","volume":"258","author":"AMR Taylor","year":"1975","unstructured":"Taylor AMR, Harnden DG, Arlett CF, Harcourt SA, Stevens S, Bridges BA (1975) Ataxia telangiectasia: A human mutation with abnormal radiation sensitivity. Nature 258:427?429","journal-title":"Nature"}],"container-title":["Human Genetics"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/BF00290214.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/article\/10.1007\/BF00290214\/fulltext.html","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/BF00290214","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2020,4,3]],"date-time":"2020-04-03T08:13:23Z","timestamp":1585901603000},"score":1,"resource":{"primary":{"URL":"http:\/\/link.springer.com\/10.1007\/BF00290214"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[1980,9]]},"references-count":18,"journal-issue":{"issue":"3","published-print":{"date-parts":[[1980,9]]}},"alternative-id":["BF00290214"],"URL":"https:\/\/doi.org\/10.1007\/bf00290214","relation":{},"ISSN":["0340-6717","1432-1203"],"issn-type":[{"value":"0340-6717","type":"print"},{"value":"1432-1203","type":"electronic"}],"subject":[],"published":{"date-parts":[[1980,9]]}}}