Retinal abnormalities in three genetic disorders involving the X chromosome
Uloženo v:
| Vydáno v: | Journal francais d'ophtalmologie Ročník 43; číslo 10; s. 1107 |
|---|---|
| Hlavní autoři: | , , , , |
| Médium: | Journal Article |
| Jazyk: | francouzština |
| Vydáno: |
France
01.12.2020
|
| Témata: | |
| ISSN: | 1773-0597, 1773-0597 |
| On-line přístup: | Zjistit podrobnosti o přístupu |
| Tagy: |
Přidat tag
Žádné tagy, Buďte první, kdo vytvoří štítek k tomuto záznamu!
|
| Author | El Matri, K Chaker, N Falfoul, Y El Leuch, I E El Matri, L |
|---|---|
| Author_xml | – sequence: 1 givenname: Y surname: Falfoul fullname: Falfoul, Y email: yosra.falfoul@yahoo.fr organization: Service B, laboratoire d'oculo-génétique LR14SP01, institut Hédi Raies d'ophtalmologie de Tunis, Tunis, Tunisie. Electronic address: yosra.falfoul@yahoo.fr – sequence: 2 givenname: I E surname: El Leuch fullname: El Leuch, I E organization: Service B, laboratoire d'oculo-génétique LR14SP01, institut Hédi Raies d'ophtalmologie de Tunis, Tunis, Tunisie – sequence: 3 givenname: K surname: El Matri fullname: El Matri, K organization: Service B, laboratoire d'oculo-génétique LR14SP01, institut Hédi Raies d'ophtalmologie de Tunis, Tunis, Tunisie – sequence: 4 givenname: N surname: Chaker fullname: Chaker, N organization: Service B, laboratoire d'oculo-génétique LR14SP01, institut Hédi Raies d'ophtalmologie de Tunis, Tunis, Tunisie – sequence: 5 givenname: L surname: El Matri fullname: El Matri, L organization: Service B, laboratoire d'oculo-génétique LR14SP01, institut Hédi Raies d'ophtalmologie de Tunis, Tunis, Tunisie |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/32829937$$D View this record in MEDLINE/PubMed |
| BookMark | eNpNkEtLw0AUhQep2Fr7A9xIlm4S55V5LKX4woIgCu7CJLnTTklm6kxa8N8bsYJw4Fw4H4fLOUcTHzwgdElwQTARN9tia0NBMcUFJqPkCZoRKVmOSy0n_-4pWqTkaky0oLIsyRmaMqqo1kzO0PMrDM6bLjO1D7E3nRscpMz5bNhEgGwNfgSarHUpxBbiT3QI3cH59UhA9pE1mxj6kEIPF-jUmi7B4uhz9H5_97Z8zFcvD0_L21W-I5wMeUMaq3WrWE2I5lpaLBimrRBk_M6ImlkNlmhjqAWpammV4opxqwTntDGMztH1b-8uhs89pKHqXWqg64yHsE8V5UwooXFZjujVEd3XPbTVLrrexK_qbwD6DYeXYHA |
| ContentType | Journal Article |
| DBID | CGR CUY CVF ECM EIF NPM 7X8 |
| DOI | 10.1016/j.jfo.2020.01.017 |
| DatabaseName | Medline MEDLINE MEDLINE (Ovid) MEDLINE MEDLINE PubMed MEDLINE - Academic |
| DatabaseTitle | MEDLINE Medline Complete MEDLINE with Full Text PubMed MEDLINE (Ovid) MEDLINE - Academic |
| Database_xml | – sequence: 1 dbid: NPM name: PubMed url: http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed sourceTypes: Index Database – sequence: 2 dbid: 7X8 name: MEDLINE - Academic url: https://search.proquest.com/medline sourceTypes: Aggregation Database |
| DeliveryMethod | no_fulltext_linktorsrc |
| DocumentTitleAlternate | Atteintes rétiniennes dans le cadre de trois anomalies génétiques impliquant le chromosome X |
| EISSN | 1773-0597 |
| ExternalDocumentID | 32829937 |
| Genre | Journal Article Case Reports |
| GroupedDBID | ABJNI ALMA_UNASSIGNED_HOLDINGS CGR CUY CVF ECM EIF NPM 7X8 |
| ID | FETCH-LOGICAL-p141t-c1cf99d83b119497f06302d661755a6b3f9ef19aa2fe78b7f884834f86442ca32 |
| IEDL.DBID | 7X8 |
| ISICitedReferencesCount | 0 |
| ISICitedReferencesURI | http://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=Summon&SrcAuth=ProQuest&DestLinkType=CitingArticles&DestApp=WOS_CPL&KeyUT=000592903500037&url=https%3A%2F%2Fcvtisr.summon.serialssolutions.com%2F%23%21%2Fsearch%3Fho%3Df%26include.ft.matches%3Dt%26l%3Dnull%26q%3D |
| ISSN | 1773-0597 |
| IngestDate | Thu Oct 02 10:31:00 EDT 2025 Thu Jan 02 22:58:23 EST 2025 |
| IsPeerReviewed | true |
| IsScholarly | true |
| Issue | 10 |
| Language | French |
| LinkModel | DirectLink |
| MergedId | FETCHMERGED-LOGICAL-p141t-c1cf99d83b119497f06302d661755a6b3f9ef19aa2fe78b7f884834f86442ca32 |
| Notes | ObjectType-Case Study-2 SourceType-Scholarly Journals-1 ObjectType-Feature-4 content type line 23 ObjectType-Report-1 ObjectType-Article-3 |
| PMID | 32829937 |
| PQID | 2436869055 |
| PQPubID | 23479 |
| ParticipantIDs | proquest_miscellaneous_2436869055 pubmed_primary_32829937 |
| PublicationCentury | 2000 |
| PublicationDate | 2020-Dec 20201201 |
| PublicationDateYYYYMMDD | 2020-12-01 |
| PublicationDate_xml | – month: 12 year: 2020 text: 2020-Dec |
| PublicationDecade | 2020 |
| PublicationPlace | France |
| PublicationPlace_xml | – name: France |
| PublicationTitle | Journal francais d'ophtalmologie |
| PublicationTitleAlternate | J Fr Ophtalmol |
| PublicationYear | 2020 |
| SSID | ssib019627551 ssib053390985 |
| Score | 2.126349 |
| SourceID | proquest pubmed |
| SourceType | Aggregation Database Index Database |
| StartPage | 1107 |
| SubjectTerms | Aicardi Syndrome - diagnosis Aicardi Syndrome - genetics Child Chromosome Aberrations Chromosome Disorders - diagnosis Chromosome Disorders - genetics Chromosomes, Human, Pair 8 - genetics Chromosomes, Human, X - genetics Eye Abnormalities - diagnosis Eye Abnormalities - genetics Female Genetic Diseases, X-Linked - diagnosis Genetic Diseases, X-Linked - genetics Humans Infant Infant, Newborn Male Retina - abnormalities Retina - diagnostic imaging Retina - pathology Trisomy - diagnosis Trisomy - genetics Turner Syndrome - diagnosis Turner Syndrome - genetics |
| Title | Retinal abnormalities in three genetic disorders involving the X chromosome |
| URI | https://www.ncbi.nlm.nih.gov/pubmed/32829937 https://www.proquest.com/docview/2436869055 |
| Volume | 43 |
| WOSCitedRecordID | wos000592903500037&url=https%3A%2F%2Fcvtisr.summon.serialssolutions.com%2F%23%21%2Fsearch%3Fho%3Df%26include.ft.matches%3Dt%26l%3Dnull%26q%3D |
| hasFullText | |
| inHoldings | 1 |
| isFullTextHit | |
| isPrint | |
| link | http://cvtisr.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwpV1JS8QwFA7qePDigtu4UcFrsFm65CQiDoI6DKLSW0nSBEe0Haejv9_32o5z8SB46aFtoLx8ffneTsiZT7mLtQ-pA_RQ6YyiqShiGjtumLSFd02C7PNdMhymWaZGncOt7tIq5zqxUdRFZdFHfs6xVTqYclF0MfmgODUKo6vdCI1l0hNAZRDVSfaDJ4aDZaJF1AuYjQpVM6WTJQmmralkHuhsUr5ePZYD8rBp5NmNMPuVdDaHz2Djv5-9SdY72hlctjjZIkt-uk1uH7DeGW5rUyJ1fWu6qwbjMpjBDrsAsIUljkHRdejER6DN0AUBb7ggC-wLZvPV1bvbIU-D68erG9oNV6ATJtmMWma9UkUqDGNKqsRj8y1ewHENItOxEV45z5TW3LskNYlPU_Q7-hQIFLda8F2yUlal2ycBLBYqssBVDBjaoTRComUjtZVgD_GiT07nsskBvBiR0KWrPut8IZ0-2WsFnE_aLhu5wBgvkKeDP6w-JGu4b22ayRHpefh13TFZtV-zcT09aVAB1-Ho_hulUb9d |
| linkProvider | ProQuest |
| openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Retinal+abnormalities+in+three+genetic+disorders+involving+the+X+chromosome&rft.jtitle=Journal+francais+d%27ophtalmologie&rft.au=Falfoul%2C+Y&rft.au=El+Leuch%2C+I+E&rft.au=El+Matri%2C+K&rft.au=Chaker%2C+N&rft.date=2020-12-01&rft.eissn=1773-0597&rft.volume=43&rft.issue=10&rft.spage=1107&rft_id=info:doi/10.1016%2Fj.jfo.2020.01.017&rft_id=info%3Apmid%2F32829937&rft_id=info%3Apmid%2F32829937&rft.externalDocID=32829937 |
| thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1773-0597&client=summon |
| thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1773-0597&client=summon |
| thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1773-0597&client=summon |