{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2024,3,19]],"date-time":"2024-03-19T11:03:08Z","timestamp":1710846188302},"reference-count":15,"publisher":"Springer Science and Business Media LLC","issue":"1","license":[{"start":{"date-parts":[[1979,8,1]],"date-time":"1979-08-01T00:00:00Z","timestamp":302313600000},"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":[[1979,8]]},"DOI":"10.1007\/bf00295585","type":"journal-article","created":{"date-parts":[[2004,11,8]],"date-time":"2004-11-08T03:56:17Z","timestamp":1099886177000},"page":"29-32","source":"Crossref","is-referenced-by-count":8,"title":["Moderate mental retardation and nonspecific dysmorphic syndrome associated with ring chromosome 9"],"prefix":"10.1007","volume":"50","author":[{"given":"J. P.","family":"Fryns","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"A.","family":"Lambrechts","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"H.","family":"Jansseune","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"H.","family":"Van den Berghe","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"297","reference":[{"key":"CR1","doi-asserted-by":"crossref","first-page":"1","DOI":"10.1111\/j.1469-1809.1966.tb00001.x","volume":"30","author":"L. Atkins","year":"1966","unstructured":"Atkins L., Pant, S. S., Hazard, G. W., Ovelette, E. M.: Two cases with a C-group ring chromosome. Ann. Hum. Genet. 30, 1?5 (1966)","journal-title":"Ann. Hum. Genet."},{"key":"CR2","first-page":"29","volume":"17","author":"H. Berghe Van den","year":"1974","unstructured":"Berghe, H. Van den, Fryns, J. P., Cassiman, J. J., David, G.: Chromosome 6 en anneau. Caryotype 46,XY,r(6)\/45,XY,-6. Ann. Genet. (Paris) 17, 29?35 (1974)","journal-title":"Ann. Genet. (Paris)"},{"key":"CR3","doi-asserted-by":"crossref","first-page":"195","DOI":"10.1007\/BF00295414","volume":"44","author":"J. Deroover","year":"1978","unstructured":"Deroover, J., Fryns, J. P., Parloir, C., Haegeman, J., Berghe, H. Van den: Partial monosomy of the short arm of chromosome 9. Hum. Genet. 44, 195?200 (1978)","journal-title":"Hum. Genet."},{"key":"CR4","first-page":"175","volume":"17","author":"J. Fraisse","year":"1974","unstructured":"Fraisse, J., Lauras, B., Ooghe, M. J., Freycon, F., Rethor\u00e9, M. O.: A propos d'un cas de chromosome 9 en anneau. Identification par d\u00e9naturation m\u00e9nag\u00e9e. Ann. Genet. (Paris) 17, 175?180 (1974)","journal-title":"Ann. Genet. (Paris)"},{"key":"CR5","doi-asserted-by":"crossref","first-page":"177","DOI":"10.1136\/jmg.7.2.177","volume":"7","author":"G. Gacs","year":"1970","unstructured":"Gacs, G., Schuler, D., Sellyei, M.: Familial occurrence of congenital malformation and ring chromosome (46,XX,Cr). J. Med. Genet. 7, 177?179 (1970)","journal-title":"J. Med. Genet."},{"key":"CR6","doi-asserted-by":"crossref","first-page":"434","DOI":"10.1111\/j.1399-0004.1973.tb01173.x","volume":"4","author":"P. Jacobsen","year":"1973","unstructured":"Jacobsen, P., Mikkelsen, M., Rosleff, F.: A ring chromosome, diagnosed by quinacrine fluorescence as no. 9, in a mentally retarded girl. Clin. Genet. 4, 434?441 (1973)","journal-title":"Clin. Genet."},{"key":"CR7","doi-asserted-by":"crossref","first-page":"122","DOI":"10.1159\/000130508","volume":"15","author":"M. L. Kistenmacher","year":"1975","unstructured":"Kistenmacher, M. L., Punnett, H. H., Aronson, M., Miller, R. C., Greene, A. E., Coriell, L. L.: A ring 9 chromosome. Repository identification No. GM-166. Cytogenet. Cell Genet. 15, 122?123 (1975)","journal-title":"Cytogenet. Cell Genet."},{"key":"CR8","doi-asserted-by":"crossref","first-page":"351","DOI":"10.1007\/BF00393619","volume":"37","author":"C. Metaxatou","year":"1977","unstructured":"Metaxatou, C., Kalpini-Mavrou, A.: Ring chromosome 9 46,XY,r(9) in a male with ambiguous external genitalia. Hum. Genet. 37, 351?354 (1977)","journal-title":"Hum. Genet."},{"key":"CR9","doi-asserted-by":"crossref","first-page":"289","DOI":"10.1007\/BF00295818","volume":"32","author":"S. Nakajima","year":"1976","unstructured":"Nakajima, S., Yanigisawa, M., Kamoshita, S., Nakogome, Y.: Mental retardation and congenital malformations associated with a ring chromosome 9. Hum. Genet. 32, 289?293 (1976)","journal-title":"Hum. Genet."},{"key":"CR10","doi-asserted-by":"crossref","first-page":"226","DOI":"10.1111\/j.1399-0004.1972.tb04271.x","volume":"3","author":"M. S. Newton","year":"1972","unstructured":"Newton, M. S., Cummingham, C., Jacobs, P. A., Price, W. H., Fraser, I. A.: Chromosome survey of a hospital for the mentally subnormal. Part 2. Autosomal abnormalities. Clin. Genet. 3, 226?248 (1972)","journal-title":"Clin. Genet."},{"key":"CR11","doi-asserted-by":"crossref","first-page":"63","DOI":"10.1136\/jmg.14.1.63","volume":"14","author":"R. A. Pfeiffer","year":"1977","unstructured":"Pfeiffer, R. A., Dhadial, R., Lenz, W.: 46,XX\/46,XX,r(15) mosaicism. Report of a case. J. Med. Genet. 14, 63?65 (1977)","journal-title":"J. Med. Genet."},{"key":"CR12","first-page":"232","volume":"20","author":"B. Sele","year":"1977","unstructured":"Sele, B., Joannard, A., Jalbert, P., Boucharlat, J.: Ring chromosome 6. A non-specific clinical picture. Ann. G\u00e9n\u00e9t. 20, 232?236 (1977)","journal-title":"Ann. G\u00e9n\u00e9t."},{"key":"CR13","doi-asserted-by":"crossref","first-page":"561","DOI":"10.1159\/000152623","volume":"23","author":"G. F. Smith","year":"1973","unstructured":"Smith, G. F., Sachdeva, S., Justice, P.: A chromosome break and partial deletion of a number 9 chromosome. Hum. Hered. 23, 561?567 (1973)","journal-title":"Hum. Hered."},{"key":"CR14","doi-asserted-by":"crossref","first-page":"227","DOI":"10.1136\/jmg.8.2.227","volume":"8","author":"A. J. Therkelsen","year":"1971","unstructured":"Therkelsen, A. J., Moler, B., Henningsen, K.: A group C ring chromosome in a mentally deficient. J. Med. Genet. 8, 227?230 (1971)","journal-title":"J. Med. Genet."},{"key":"CR15","doi-asserted-by":"crossref","first-page":"193","DOI":"10.1007\/BF00281453","volume":"26","author":"R. Zdansky","year":"1975","unstructured":"Zdansky, R., Andrle, M., Buhler, E., Tsuchimoto, T., Mayr, W. R., Rett, A.: Irregular phenotypic expression of ring chromosomes. Humangenetik 26, 193?198 (1975)","journal-title":"Humangenetik"}],"container-title":["Human Genetics"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/BF00295585.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/article\/10.1007\/BF00295585\/fulltext.html","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/BF00295585","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2023,4,30]],"date-time":"2023-04-30T00:59:57Z","timestamp":1682816397000},"score":1,"resource":{"primary":{"URL":"http:\/\/link.springer.com\/10.1007\/BF00295585"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[1979,8]]},"references-count":15,"journal-issue":{"issue":"1","published-print":{"date-parts":[[1979,8]]}},"alternative-id":["BF00295585"],"URL":"https:\/\/doi.org\/10.1007\/bf00295585","relation":{},"ISSN":["0340-6717","1432-1203"],"issn-type":[{"value":"0340-6717","type":"print"},{"value":"1432-1203","type":"electronic"}],"subject":[],"published":{"date-parts":[[1979,8]]}}}