{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2024,7,10]],"date-time":"2024-07-10T19:57:10Z","timestamp":1720641430096},"reference-count":5,"publisher":"Elsevier BV","license":[{"start":{"date-parts":[[2018,7,1]],"date-time":"2018-07-01T00:00:00Z","timestamp":1530403200000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"}],"content-domain":{"domain":["clinicalkey.jp","clinicalkey.com","clinicalkey.es","clinicalkey.com.au","clinicalkey.fr","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Seminars in Pediatric Neurology"],"published-print":{"date-parts":[[2018,7]]},"DOI":"10.1016\/j.spen.2017.03.007","type":"journal-article","created":{"date-parts":[[2017,4,1]],"date-time":"2017-04-01T11:00:52Z","timestamp":1491044452000},"page":"60-62","update-policy":"http:\/\/dx.doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":2,"special_numbering":"C","title":["Consideration of Genetic Diagnoses of Developmental Delay in Children of Consanguineous Families"],"prefix":"10.1016","volume":"26","author":[{"given":"Salva","family":"Sadeghi","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Michael","family":"Shevell","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"key":"10.1016\/j.spen.2017.03.007_bib1","doi-asserted-by":"crossref","first-page":"391","DOI":"10.1016\/S0168-9525(98)01556-X","article-title":"Use of isolated inbred human populations for identification of disease genes","volume":"14","author":"Sheffield","year":"1998","journal-title":"Trends Genet"},{"issue":"1","key":"10.1016\/j.spen.2017.03.007_bib2","first-page":"1","article-title":"The frequency of consanguineous marriages and their effects on offsprings in Tabriz city","volume":"11","author":"Rahmani","year":"2010","journal-title":"Shiraz E-Med J"},{"key":"10.1016\/j.spen.2017.03.007_bib3","first-page":"182","article-title":"Preventable fraction of mental retardation: Analysis based on individuals with severe mental retardation","volume":"34","author":"Stevenson","year":"1996","journal-title":"Ment Retard"},{"key":"10.1016\/j.spen.2017.03.007_bib4","doi-asserted-by":"crossref","unstructured":"Michelson DJ, Shevell MI, Sherr EH, Moeschler JB, Gropman AL, Ashwal S: Evidence Report: Genetic and metabolic testing on children with global developmental delay. Report of the Quality Standards Subcommittee of the American Academy of Neurology and the Practice Committee of the Child Neurology Society. American Academy of Neurology, 2011","DOI":"10.1212\/WNL.0b013e3182345896"},{"key":"10.1016\/j.spen.2017.03.007_bib5","doi-asserted-by":"crossref","first-page":"367","DOI":"10.1212\/01.WNL.0000031431.81555.16","article-title":"Practice parameter: Evaluation of the child with global developmental delay","volume":"60","author":"Shevell","year":"2003","journal-title":"Neurology"}],"container-title":["Seminars in Pediatric Neurology"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1071909117300232?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1071909117300232?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2019,9,20]],"date-time":"2019-09-20T10:10:53Z","timestamp":1568974253000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S1071909117300232"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2018,7]]},"references-count":5,"alternative-id":["S1071909117300232"],"URL":"https:\/\/doi.org\/10.1016\/j.spen.2017.03.007","relation":{},"ISSN":["1071-9091"],"issn-type":[{"value":"1071-9091","type":"print"}],"subject":[],"published":{"date-parts":[[2018,7]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Consideration of Genetic Diagnoses of Developmental Delay in Children of Consanguineous Families","name":"articletitle","label":"Article Title"},{"value":"Seminars in Pediatric Neurology","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.spen.2017.03.007","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"Crown Copyright \u00a9 2017 Published by Elsevier Inc. All rights reserved.","name":"copyright","label":"Copyright"}]}}