{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,10,18]],"date-time":"2025-10-18T10:17:35Z","timestamp":1760782655615},"reference-count":17,"publisher":"Springer Science and Business Media LLC","issue":"2","license":[{"start":{"date-parts":[[1983,12,1]],"date-time":"1983-12-01T00:00:00Z","timestamp":439084800000},"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":[[1983,12]]},"DOI":"10.1007\/bf00286649","type":"journal-article","created":{"date-parts":[[2004,10,5]],"date-time":"2004-10-05T08:37:16Z","timestamp":1096965436000},"page":"134-138","source":"Crossref","is-referenced-by-count":25,"title":["Interstitial deletion for a region in the long arm of chromosome 16"],"prefix":"10.1007","volume":"65","author":[{"given":"C. C.","family":"Lin","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"R. B.","family":"Lowry","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"F. F.","family":"Snyder","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"297","reference":[{"key":"CR1","first-page":"171","volume":"23","author":"GB C\u00f4t\u00e9","year":"1980","unstructured":"C\u00f4t\u00e9 GB, Papadakou-Lagoyanni S, Kairis M (1980) Fryns syndrome without deletion 16q. Ann Genet (Paris)23: 171?172","journal-title":"Ann Genet (Paris)"},{"key":"CR2","doi-asserted-by":"crossref","first-page":"161","DOI":"10.1159\/000131696","volume":"32","author":"MA Ferguson-Smith","year":"1982","unstructured":"Ferguson-Smith MA, Westerveld A (1982) Report of the committee on the genetic constitution of chromosomes 13 to 22. Cytogenet Cell Genet 32: 161?178","journal-title":"Cytogenet Cell Genet"},{"key":"CR3","doi-asserted-by":"crossref","unstructured":"Fryns JP (1983) Personal communication","DOI":"10.1111\/j.1399-0004.1983.tb00443.x"},{"key":"CR4","doi-asserted-by":"crossref","first-page":"343","DOI":"10.1007\/BF00402162","volume":"38","author":"JP Fryns","year":"1977","unstructured":"Fryns JP, Melchior S, Jaeken J, van den Berghe H (1977) Partial monosomy of the long arm of chromosome 16 in a malformed newborn: karyotype 46,XX,del(16)(q21). Hum Genet 38: 343?346","journal-title":"Hum Genet"},{"key":"CR5","doi-asserted-by":"crossref","first-page":"115","DOI":"10.1007\/BF00278910","volume":"46","author":"JP Fryns","year":"1979","unstructured":"Fryns JP, Bande-Knops J, van den Berghe H (1979) Partial monosomy of the long arm of chromosome 16: a distinct clinical entity? Hum Genet 46: 115?120","journal-title":"Hum Genet"},{"key":"CR6","first-page":"124","volume":"24","author":"JP Fryns","year":"1981","unstructured":"Fryns JP, Proesmans W, van Hoey G, van den Berghe H (1981) Interstitial 16q deletion with typical dysmorphic syndrome. Ann Genet 24: 124?125","journal-title":"Ann Genet"},{"key":"CR7","doi-asserted-by":"crossref","first-page":"1284","DOI":"10.1126\/science.197600","volume":"197","author":"MS Hershfield","year":"1977","unstructured":"Hershfield MS, Snyder FF, Seegmiller JE (1977) Adenine and adenosine are toxic to human lymphoblast mutants defective in purine salvage enzymes. Science 197: 1284?1287","journal-title":"Science"},{"key":"CR8","doi-asserted-by":"crossref","first-page":"15","DOI":"10.2183\/pjab.55.15","volume":"55","author":"T Ikeuchi","year":"1979","unstructured":"Ikeuchi T, Sasaki M (1979) Accumulation of early mitotic cells in ethidium bromide-treated human lymphocyte cultures. Proc Jap Acad 55: 15?18","journal-title":"Proc Jap Acad"},{"key":"CR9","doi-asserted-by":"crossref","first-page":"403","DOI":"10.1016\/0003-2697(79)90678-X","volume":"92","author":"GG Johnson","year":"1979","unstructured":"Johnson GG, Littlefield JW (1979) Assay of hypoxanthine-guanine phosphoribosyltransferase in human fibroblasts lysates: inactivation of nucleotidase. Anal Biochem 92: 403?410","journal-title":"Anal Biochem"},{"key":"CR10","doi-asserted-by":"crossref","first-page":"937","DOI":"10.1007\/BF00918878","volume":"4","author":"CC Lin","year":"1978","unstructured":"Lin CC, Biederman B, Jamro H, (1978) Q-banding methods using quinacrine (QFQ) and Hoechst 33258 (QFH) for chromosome analysis of human lymphocyte cultures. TCA Manual 4: 937?940","journal-title":"TCA Manual"},{"key":"CR11","doi-asserted-by":"crossref","first-page":"204","DOI":"10.1038\/256204a0","volume":"256","author":"B Marimo","year":"1975","unstructured":"Marimo B, Giannelli F (1975) Gene dosage effect in human trisomy 16. Nature 256: 204?206","journal-title":"Nature"},{"key":"CR12","doi-asserted-by":"crossref","first-page":"307","DOI":"10.1007\/BF00292840","volume":"58","author":"D Schweizer","year":"1976","unstructured":"Schweizer D (1976) Reverse fluorescent chromosome banding with chromomycin and DAPI. Chromosoma 58: 307?324","journal-title":"Chromosoma"},{"key":"CR13","doi-asserted-by":"crossref","first-page":"304","DOI":"10.1016\/0014-4827(72)90558-7","volume":"75","author":"AT Sumner","year":"1972","unstructured":"Sumner AT (1972) A simple C-banding method. Exp Cell Res 75: 304?305","journal-title":"Exp Cell Res"},{"key":"CR14","first-page":"343","volume":"14","author":"K Taysi","year":"1978","unstructured":"Taysi K, Fishman M, Sekhon GS (1978) A terminal long arm deletion of chromosome 16 in a dysmorphic infant: 46,XY,del(16)(q22). Birth Defects 14: 343?347","journal-title":"Birth Defects"},{"key":"CR15","unstructured":"Taysi K (1983) Personal communication"},{"key":"CR16","doi-asserted-by":"crossref","first-page":"45","DOI":"10.1073\/pnas.71.1.45","volume":"71","author":"JA Tischfield","year":"1974","unstructured":"Tischfield JA, Ruddle FH (1974) Assignment of the gene for adenine phosphoribosyltransferase to human chromosome 16 by mouse-human somatic cell hybridization. Proc Natl Acad Sci USA 71: 45?49","journal-title":"Proc Natl Acad Sci USA"},{"key":"CR17","first-page":"47","volume":"6","author":"HC Wang","year":"1972","unstructured":"Wang HC, Federoff S (1972) Banding human chromosomes with trypsin. Cytobios 6: 47?74","journal-title":"Cytobios"}],"container-title":["Human Genetics"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/BF00286649.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/article\/10.1007\/BF00286649\/fulltext.html","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/BF00286649","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2019,4,8]],"date-time":"2019-04-08T21:06:11Z","timestamp":1554757571000},"score":1,"resource":{"primary":{"URL":"http:\/\/link.springer.com\/10.1007\/BF00286649"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[1983,12]]},"references-count":17,"journal-issue":{"issue":"2","published-print":{"date-parts":[[1983,12]]}},"alternative-id":["BF00286649"],"URL":"https:\/\/doi.org\/10.1007\/bf00286649","relation":{},"ISSN":["0340-6717","1432-1203"],"issn-type":[{"value":"0340-6717","type":"print"},{"value":"1432-1203","type":"electronic"}],"subject":[],"published":{"date-parts":[[1983,12]]}}}