{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,4,6]],"date-time":"2026-04-06T17:22:04Z","timestamp":1775496124531,"version":"3.50.1"},"reference-count":19,"publisher":"Springer Science and Business Media LLC","issue":"3","license":[{"start":{"date-parts":[[2009,8,1]],"date-time":"2009-08-01T00:00:00Z","timestamp":1249084800000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/www.springer.com\/tdm"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["World J Pediatr"],"published-print":{"date-parts":[[2009,8]]},"DOI":"10.1007\/s12519-009-0042-1","type":"journal-article","created":{"date-parts":[[2009,8,19]],"date-time":"2009-08-19T11:15:44Z","timestamp":1250680544000},"page":"222-225","source":"Crossref","is-referenced-by-count":6,"title":["Constitutional retinoblastoma gene deletion in Egyptian patients"],"prefix":"10.1007","volume":"5","author":[{"given":"Amal M.","family":"Mohammed","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Alaa K.","family":"Kamel","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Saida A.","family":"Hammad","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Hanan H.","family":"Afifi","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Zeinab","family":"El Sanabary","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Mostafa Ezz","family":"El Din","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"297","published-online":{"date-parts":[[2009,8,20]]},"reference":[{"key":"42_CR1","unstructured":"OMIM. Online Mendelian Inheritance in Man. 2008, Center for Medical Genetics, John Hopkins University (Baltimore, M.D.) and National Center for Biotechnology Information, National Library of Medicine (Bethesda, MD). http:\/\/www.ncbi.nlm.nih.gov\/OMIM (accessed September 3, 2008)"},{"key":"42_CR2","doi-asserted-by":"crossref","first-page":"149","DOI":"10.1016\/S0031-3955(02)00115-3","volume":"50","author":"B. Castillo","year":"2003","unstructured":"Castillo B, Kaufman L. Pediatric tumors of the eye and orbit. Pediatr Clin North Am 2003;50:149\u2013172.","journal-title":"Pediatr Clin North Am"},{"key":"42_CR3","first-page":"1039","volume":"73","author":"A. Melamud","year":"2006","unstructured":"Melamud A, Palekar R, Singh A. Retinoblastoma. Am Fam Physician 2006;73:1039\u20131044.","journal-title":"Am Fam Physician"},{"key":"42_CR4","doi-asserted-by":"crossref","first-page":"5341","DOI":"10.1038\/sj.onc.1209622","volume":"25","author":"A. Balmer","year":"2006","unstructured":"Balmer A, Zografos L, Munier F. Diagnosis and current management of retinoblastoma. Oncogene 2006;25:5341\u20135349.","journal-title":"Oncogene"},{"key":"42_CR5","unstructured":"Medical Encyclopedia, 2008. http:\/\/www.answers.com\/topic\/retinoblastoma (accessed September 3, 2008)."},{"key":"42_CR6","doi-asserted-by":"crossref","first-page":"33","DOI":"10.1016\/j.cancergencyto.2003.08.015","volume":"150","author":"P.S. Amare Kadam","year":"2004","unstructured":"Amare Kadam PS, Ghule P, Jose J, Bamne M, Kurkure P, Banavali S, et al. Constitutional genomic instability, chromosomal aberrations in tumor cells and retinoblastoma. Cancer Genet Cytogenet 2004;150:33\u201343.","journal-title":"Cancer Genet Cytogenet"},{"key":"42_CR7","first-page":"348","volume":"76","author":"A.B. Silverstein","year":"1971","unstructured":"Silverstein AB. Deviation social quotients for the Vineland social maturity scale. Am J Ment Defic 1971;76:348\u2013351.","journal-title":"Am J Ment Defic"},{"key":"42_CR8","doi-asserted-by":"crossref","first-page":"377","DOI":"10.1111\/j.1365-2214.1992.tb00367.x","volume":"18","author":"P. Sturmey","year":"1992","unstructured":"Sturmey P, Thorburn MJ, Brown JM, Reed J, Kaur J, King G. Portage guide to early intervention: cross-cultural aspects and intra-cultural variability. Child Care Health Dev 1992;18:377\u2013394.","journal-title":"Child Care Health Dev"},{"key":"42_CR9","volume-title":"Human Chromosomes: Principal and Techniques","author":"R.S. Verma","year":"1995","unstructured":"Verma RS, Babu A. Human Chromosomes: Principal and Techniques, 2nd ed. New York, San Francisco: Mc Graw-Hill Inc., 1995.","edition":"2nd ed"},{"key":"42_CR10","volume-title":"An International System for Human Cytogenetic Nomenclature (ISCN)","author":"L.G. Shaffer","year":"2005","unstructured":"Shaffer LG, Tommerup N. An International System for Human Cytogenetic Nomenclature (ISCN). Basel: Karger, 2005."},{"issue":"Pt1","key":"42_CR11","doi-asserted-by":"crossref","first-page":"151","DOI":"10.1101\/SQB.1986.051.01.018","volume":"51","author":"D. Pinkel","year":"1986","unstructured":"Pinkel D, Gray JW, Trask B, van den Engh G, Fuscoe J, van Dekken H. Cytogenetic analysis by in situ hybridization with fluorescently labeled nucleic acid probes. Cold Spring Harb Symp Quant Biol 1986;51Pt 1:151\u2013157.","journal-title":"Cold Spring Harb Symp Quant Biol"},{"key":"42_CR12","doi-asserted-by":"crossref","first-page":"57","DOI":"10.1016\/S0092-8674(00)81683-9","volume":"100","author":"D. Hanahan","year":"2000","unstructured":"Hanahan D, Weinberg RA. The hallmarks of cancer. Cell 2000;100:57\u201370.","journal-title":"Cell"},{"key":"42_CR13","doi-asserted-by":"crossref","first-page":"478","DOI":"10.1034\/j.1399-0004.1999.550614.x","volume":"55","author":"O. Baud","year":"1999","unstructured":"Baud O, Cormier-Daire V, Lyonnet S, Desjardins L, Turleau C, Doz F. Dysmorphic phenotype and neurological impairment in 22 retinoblastoma patients with constitutional cytogenetic 13q deletion. Clin Genet 1999;55:478\u2013482.","journal-title":"Clin Genet"},{"key":"42_CR14","doi-asserted-by":"crossref","first-page":"11","DOI":"10.1076\/opge.22.1.11.2235","volume":"22","author":"R.I. Bojinova","year":"2001","unstructured":"Bojinova RI, Schorderet DF, Addor MC, Gaide AC, Thonney F, Pescia G, et al. Further delineation of the facial 13q14 deletion syndrome in 13 retinoblastoma patients. Ophthalmic Genet 2001;22:11\u201318.","journal-title":"Ophthalmic Genet"},{"key":"42_CR15","doi-asserted-by":"crossref","first-page":"58","DOI":"10.1136\/jmg.20.1.58","volume":"20","author":"M. Hafez","year":"1983","unstructured":"Hafez M, El-Tahan H, Awadalla M, El-Khayat H, Abdel-Gafar A, Ghoneim M. Consanguineous matings in the Egyptian population. J Med Genet 1983;20:58\u201360.","journal-title":"J Med Genet"},{"key":"42_CR16","doi-asserted-by":"crossref","first-page":"29","DOI":"10.1016\/0165-4608(82)90018-8","volume":"6","author":"M.P. Johnson","year":"1982","unstructured":"Johnson MP, Ramsay N, Cervenka J, Wang N. Retinoblastoma and its association with deletion in chromosome 13: a survey using high-resolution chromosome technique. Cancer Genet Cytogenet 1982;6:29\u201337.","journal-title":"Cancer Genet Cytogenet"},{"key":"42_CR17","doi-asserted-by":"crossref","first-page":"321","DOI":"10.1016\/0165-4608(85)90240-7","volume":"16","author":"C. Turleau","year":"1985","unstructured":"Turleau C, de Grouchy J, Chavin-Colin F, Junien C, S\u00e9ger J, Schlienger P, et al. Cytogenetic forms of retinoblastoma: their incidence in a survey of 66 patients. Cancer Genet Cytogenet 1985;16:321\u2013334.","journal-title":"Cancer Genet Cytogenet"},{"key":"42_CR18","doi-asserted-by":"crossref","first-page":"598","DOI":"10.1002\/pbc.21687","volume":"51","author":"R.H. Barbosa","year":"2008","unstructured":"Barbosa RH, Vergas FR, Aguiar FC. Ferman S, Lucena E, Bovicino CR, et al. Hereditary retinoblastoma transmitted by maternal germline mosaicism. Pediatr Blood Cancer 2008;51:598\u2013602.","journal-title":"Pediatr Blood Cancer"},{"key":"42_CR19","doi-asserted-by":"crossref","first-page":"174","DOI":"10.1086\/341284","volume":"71","author":"M. Klutz","year":"2002","unstructured":"Klutz M, Brockmann D, Lohmann DR. A parent-of-origin effect in two families with retinoblastoma is associated with a distinct splice mutation in the Rb1 gene. Am J Hum Genet 2002;71:174\u2013179.","journal-title":"Am J Hum Genet"}],"container-title":["World Journal of Pediatrics"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/s12519-009-0042-1.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/article\/10.1007\/s12519-009-0042-1\/fulltext.html","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/s12519-009-0042-1","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2019,6,2]],"date-time":"2019-06-02T11:58:43Z","timestamp":1559476723000},"score":1,"resource":{"primary":{"URL":"http:\/\/link.springer.com\/10.1007\/s12519-009-0042-1"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2009,8]]},"references-count":19,"journal-issue":{"issue":"3","published-print":{"date-parts":[[2009,8]]}},"alternative-id":["42"],"URL":"https:\/\/doi.org\/10.1007\/s12519-009-0042-1","relation":{},"ISSN":["1708-8569","1867-0687"],"issn-type":[{"value":"1708-8569","type":"print"},{"value":"1867-0687","type":"electronic"}],"subject":[],"published":{"date-parts":[[2009,8]]}}}