{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2022,3,29]],"date-time":"2022-03-29T19:59:21Z","timestamp":1648583961302},"reference-count":10,"publisher":"Springer Science and Business Media LLC","issue":"4","license":[{"start":{"date-parts":[[1996,12,1]],"date-time":"1996-12-01T00:00:00Z","timestamp":849398400000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/www.springer.com\/tdm"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Journal of Tongji Medical University"],"published-print":{"date-parts":[[1996,12]]},"DOI":"10.1007\/bf02888117","type":"journal-article","created":{"date-parts":[[2010,6,23]],"date-time":"2010-06-23T21:16:08Z","timestamp":1277327768000},"page":"245-248","source":"Crossref","is-referenced-by-count":0,"title":["Study on the relationship between cytogenetics and phenotypic effect in Turner\u2019s syndrome"],"prefix":"10.1007","volume":"16","author":[{"given":"Hu","family":"Xiaofeng","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Zhu","family":"Baosheng","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Lin","family":"Hanhua","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Shu","family":"Dan","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Tao","family":"Deding","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Wang","family":"Mudi","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"297","reference":[{"key":"BF02888117_CR1","doi-asserted-by":"crossref","first-page":"37","DOI":"10.1007\/BF00270556","volume":"67","author":"M Camarg","year":"1984","unstructured":"Camarg M, Cervenka J. DNA replication and inactivation patterns in structural abnormality of sex chromosomes. Hum Genet, 1984, 67:37","journal-title":"Hum Genet"},{"key":"BF02888117_CR2","unstructured":"t(X:X)DNA 1988, 5(1): 15"},{"key":"BF02888117_CR3","first-page":"757","volume":"34","author":"M Camargo","year":"1982","unstructured":"Camargo M, Cervenka J. Patterns of DNA replication of human chromosomes. II. Replication map and replication model. Am J Hum Genet, 1982, 34:757","journal-title":"Am J Hum Genet"},{"key":"BF02888117_CR4","first-page":"313","volume":"21","author":"ISCN","year":"1978","unstructured":"ISCN. An international system for human cytogenetic nomenclature. Cytogenet Cell Genet, 1978, 21,21:313","journal-title":"Cytogenet Cell Genet"},{"key":"BF02888117_CR5","doi-asserted-by":"crossref","first-page":"145","DOI":"10.1111\/j.1399-0004.1982.tb00752.x","volume":"21","author":"D Wyss","year":"1982","unstructured":"Wyss D, Delozier C D, Daniell J. Structural anomalities of the X chromosome: personal obseration and review of non-mosaic cases. Clin Genet, 1982, 21:145","journal-title":"Clin Genet"},{"key":"BF02888117_CR6","first-page":"175","volume":"85","author":"E Therman","year":"1990","unstructured":"Therman E, Susman B. The similarity of phenotypic effects caused by Xp and Xq deletion in the human female: a hypothesis. Hum Genet, 1990, 85:175","journal-title":"Hum Genet"},{"key":"BF02888117_CR7","doi-asserted-by":"crossref","first-page":"147","DOI":"10.1111\/j.1399-0004.1992.tb03652.x","volume":"41","author":"S A Temtamy","year":"1992","unstructured":"Temtamy S A, Ghali I, Salam M A. Karyotype\/phenotype correlation in females with short stature. Clin Genet, 1992, 41:147","journal-title":"Clin Genet"},{"key":"BF02888117_CR8","doi-asserted-by":"crossref","first-page":"59","DOI":"10.1007\/BF00295590","volume":"50","author":"E Therman","year":"1979","unstructured":"Therman E, Sarto G E, Palmerc G. Position of the human X inaction center on Xq. Hum Genet, 1979, 50:59","journal-title":"Hum Genet"},{"key":"BF02888117_CR9","first-page":"455","volume":"85","author":"E Therman","year":"1990","unstructured":"Therman E, Laxova RSusman B. The critical region on the human Xq. Hum Genet, 1990, 85:455","journal-title":"Hum Genet"},{"key":"BF02888117_CR10","doi-asserted-by":"crossref","unstructured":"Midro A T, Kulikowski M, Sawicka A. Familial occurrence of isodicentric X chromosome with different breakpoints. Clin Genet, 1988: 34","DOI":"10.1111\/j.1399-0004.1988.tb02855.x"}],"container-title":["Journal of Tongji Medical University"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/BF02888117.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/article\/10.1007\/BF02888117\/fulltext.html","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/BF02888117","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2019,5,22]],"date-time":"2019-05-22T21:11:37Z","timestamp":1558559497000},"score":1,"resource":{"primary":{"URL":"http:\/\/link.springer.com\/10.1007\/BF02888117"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[1996,12]]},"references-count":10,"journal-issue":{"issue":"4","published-print":{"date-parts":[[1996,12]]}},"alternative-id":["BF02888117"],"URL":"https:\/\/doi.org\/10.1007\/bf02888117","relation":{},"ISSN":["0257-716X"],"issn-type":[{"value":"0257-716X","type":"print"}],"subject":[],"published":{"date-parts":[[1996,12]]}}}