P463: A novel de novo microdeletion at 9q33.3, including LHX2, in a patient with developmental delay and autism spectrum disorder

Saved in:
Bibliographic Details
Published inGenetics in Medicine Open Vol. 1; no. 1; p. 100510
Main Authors Gagnon, Marie-France, Barnett, Sarah, Ramanathan, Subhadra, Clark, Robin, Hoppman, Nicole
Format Journal Article
LanguageEnglish
Published Elsevier Inc 2023
Elsevier
Online AccessGet full text

Cover

Loading…
ArticleNumber 100510
Author Gagnon, Marie-France
Barnett, Sarah
Ramanathan, Subhadra
Clark, Robin
Hoppman, Nicole
Author_xml – sequence: 1
  givenname: Marie-France
  surname: Gagnon
  fullname: Gagnon, Marie-France
  organization: Mayo Clinic
– sequence: 2
  givenname: Sarah
  surname: Barnett
  fullname: Barnett, Sarah
  organization: Mayo Clinic
– sequence: 3
  givenname: Subhadra
  surname: Ramanathan
  fullname: Ramanathan, Subhadra
  organization: Loma Linda University School of Medicine
– sequence: 4
  givenname: Robin
  surname: Clark
  fullname: Clark, Robin
  organization: Loma Linda University School of Medicine
– sequence: 5
  givenname: Nicole
  surname: Hoppman
  fullname: Hoppman, Nicole
  organization: Mayo Clinic
BookMark eNp9kc1qGzEUhUVJoImTF-hKDxA7dySN5AnZGJMfg6FdJJCdkKUrV2Zm5ErjhCz75tHUoXTVla4OnI97zzknJ33skZBvFcwqqOT1brYNXZwxYLwIUFfwhZyxRjRTpYQ4-Wf-Si5z3gEAaxhXXJ6R3z-E5Dd0Qfv4ii11OA6RdsGm6LDFIcSemoE2vzif8SsaetseXOi3dP34wsY_NXRvhoD9QN_C8LMgCijuuyKYEdiad2p6R81hCLmjeY92SIeOupBjcpguyKk3bcbLz3dCnu_vnpaP0_X3h9VysZ5aBhKmWCuobYNSgHTI6zkD7xvFvRfeesXm3tRNxT14KYTl4Lnx3kuoN2gNryyfkNWR66LZ6X0KnUnvOpqg_wgxbbVJQ7AtaidlI2qJbgNKOMXnMEfJrRe4caqqWWGxI6uklHNC_5dXgR470Ts9dqLHTvSxk2K6PZqwXPkaMOlsS2wWXUglk7JG-J_9A-EQlgc
ContentType Journal Article
Copyright 2023
Copyright_xml – notice: 2023
DBID 6I.
AAFTH
AAYXX
CITATION
DOA
DOI 10.1016/j.gimo.2023.100510
DatabaseName ScienceDirect Open Access Titles
Elsevier:ScienceDirect:Open Access
CrossRef
DOAJ Directory of Open Access Journals
DatabaseTitle CrossRef
Database_xml – sequence: 1
  dbid: DOA
  name: DOAJ Directory of Open Access Journals
  url: https://www.doaj.org/
  sourceTypes: Open Website
DeliveryMethod fulltext_linktorsrc
EISSN 2949-7744
ExternalDocumentID oai_doaj_org_article_d669456edb074d73808e63cf4ebd7152
10_1016_j_gimo_2023_100510
S2949774423005101
GroupedDBID .1-
.FO
0R~
0SF
6I.
AAFTH
AFRHN
AJUYK
ALMA_UNASSIGNED_HOLDINGS
AMRAJ
EBS
FDB
GROUPED_DOAJ
M~E
Z5R
AALRI
AAXUO
AAYXX
ADVLN
AFJKZ
AITUG
CITATION
ID FETCH-LOGICAL-c2060-e5705c9e6406de35820ff973ff4fcf728fa5913f0f644c30f3afff605beca31c3
IEDL.DBID DOA
ISSN 2949-7744
IngestDate Fri Oct 04 12:49:11 EDT 2024
Thu Sep 26 17:54:20 EDT 2024
Sat Jun 01 15:42:31 EDT 2024
IsDoiOpenAccess true
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Issue 1
Language English
License http://creativecommons.org/licenses/by-nc-nd/4.0
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c2060-e5705c9e6406de35820ff973ff4fcf728fa5913f0f644c30f3afff605beca31c3
OpenAccessLink https://doaj.org/article/d669456edb074d73808e63cf4ebd7152
ParticipantIDs doaj_primary_oai_doaj_org_article_d669456edb074d73808e63cf4ebd7152
crossref_primary_10_1016_j_gimo_2023_100510
elsevier_sciencedirect_doi_10_1016_j_gimo_2023_100510
PublicationCentury 2000
PublicationDate 2023
2023-00-00
2023-01-01
PublicationDateYYYYMMDD 2023-01-01
PublicationDate_xml – year: 2023
  text: 2023
PublicationDecade 2020
PublicationTitle Genetics in Medicine Open
PublicationYear 2023
Publisher Elsevier Inc
Elsevier
Publisher_xml – name: Elsevier Inc
– name: Elsevier
SSID ssj0002923736
Score 2.2493944
SourceID doaj
crossref
elsevier
SourceType Open Website
Aggregation Database
Publisher
StartPage 100510
Title P463: A novel de novo microdeletion at 9q33.3, including LHX2, in a patient with developmental delay and autism spectrum disorder
URI https://dx.doi.org/10.1016/j.gimo.2023.100510
https://doaj.org/article/d669456edb074d73808e63cf4ebd7152
Volume 1
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrV09b9swECUCT12CFG0Qp01xQ7dGCSWKlNjNKRwYQRxkSABvAk0eCxe23A87QJcC_ee5k-RaU7t0ESRBIqU7Su9IPr4T4r3JfUYdtjQxUoUkDyUmJUrWxssyifRp2mb2fHpnJo_5zUzPeqm-mBPWygO3hrsMxlgCeQxzArtQqFKWaJSPOc5DQeDT_H1T3etM8T84o7il4HnJ0z2h6zO9_AVnC2dmgOYlsz0kagT7e4DUA5nrI3HYRYcwap_qpTjA-pX4fZ8b9RFGUK-fcAkBeWcNK6bScRobNi24DdhvSl2oc1jUfrllSILbySzjY3DQ6acCj7tC2DOFHBe4dD_B1QEctcIfK2hWX37friB00pyvxeP1-OHTJOkyJyQ-k0YmqAupvUVDcB2QF8PKGG2hYsyjj0VWRqdtqqKMFA55JaNyMUbq2ZBHnUq9OhaDel3jCVOfCq199GhSpJtLVrCzxqK1kSID6Ybiw86K1ddWIKPaMce-VGzzim1etTYfiis29J8rWdy6OUEurzqXV_9y-VDonZuqLk5o8Z-KWvyl8tP_Ufkb8YKLbEdh3ooBuQPPKC7ZzN81TZC201_jZ-dt33A
link.rule.ids 315,786,790,870,2115,4043,27956,27957,27958
linkProvider Directory of Open Access Journals
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=P463%3A+A+novel+de+novo+microdeletion+at+9q33.3%2C+including+LHX2%2C+in+a+patient+with+developmental+delay+and+autism+spectrum+disorder&rft.jtitle=Genetics+in+Medicine+Open&rft.au=Gagnon%2C+Marie-France&rft.au=Barnett%2C+Sarah&rft.au=Ramanathan%2C+Subhadra&rft.au=Clark%2C+Robin&rft.date=2023&rft.pub=Elsevier+Inc&rft.issn=2949-7744&rft.volume=1&rft.issue=1&rft_id=info:doi/10.1016%2Fj.gimo.2023.100510&rft.externalDocID=S2949774423005101
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=2949-7744&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=2949-7744&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=2949-7744&client=summon