Literature DB >> 9489800

Deletion 8p syndrome.

M C Digilio, B Marino, P Guccione, A Giannotti, R Mingarelli, B Dallapiccola.   

Abstract

Mesh：

Year:  1998        PMID： 9489800

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN： 0148-7299


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  12 in total

1.  A girl with pervasive developmental disorder and complex chromosome rearrangement involving 8p and 10p.

Authors:  L Zwaigenbaum; L K Sonnenberg; T Heshka; S Eastwood; J Xu
Journal:  J Autism Dev Disord       Date:  2005-06

2.  Delineation of the critical deletion region for congenital heart defects, on chromosome 8p23.1.

Authors:  K Devriendt; G Matthijs; R Van Dael; M Gewillig; B Eyskens; H Hjalgrim; B Dolmer; J McGaughran; K Bröndum-Nielsen; P Marynen; J P Fryns; J R Vermeesch
Journal:  Am J Hum Genet       Date:  1999-04       Impact factor: 11.025

3.  The general anesthesia experience of deletion 8p syndrome patient -A case report-.

Authors:  Woo Jong Shin; Sang Duk Kim; Kyoung Hun Kim
Journal:  Korean J Anesthesiol       Date:  2011-10-22

4.  Genotype-phenotype association studies of chromosome 8p inverted duplication deletion syndrome.

Authors:  Gene S Fisch; Ryan Davis; Janey Youngblom; Jeff Gregg
Journal:  Behav Genet       Date:  2011-01-23       Impact factor: 2.805

5.  Detailed mapping of a congenital heart disease gene in chromosome 3p25.

Authors:  E K Green; M D Priestley; J Waters; C Maliszewska; F Latif; E R Maher
Journal:  J Med Genet       Date:  2000-08       Impact factor: 6.318

6.  Rare copy number variation in posttraumatic stress disorder.

Authors:  Jonathan Sebat; Caroline M Nievergelt; Adam X Maihofer; Worrawat Engchuan; Guillaume Huguet; Marieke Klein; Jeffrey R MacDonald; Omar Shanta; Bhooma Thiruvahindrapuram; Martineau Jean-Louis; Zohra Saci; Sebastien Jacquemont; Stephen W Scherer; Elizabeth Ketema; Allison E Aiello; Ananda B Amstadter; Esmina Avdibegović; Dragan Babic; Dewleen G Baker; Jonathan I Bisson; Marco P Boks; Elizabeth A Bolger; Richard A Bryant; Angela C Bustamante; Jose Miguel Caldas-de-Almeida; Graça Cardoso; Jurgen Deckert; Douglas L Delahanty; Katharina Domschke; Boadie W Dunlop; Alma Dzubur-Kulenovic; Alexandra Evans; Norah C Feeny; Carol E Franz; Aarti Gautam; Elbert Geuze; Aferdita Goci; Rasha Hammamieh; Miro Jakovljevic; Marti Jett; Ian Jones; Milissa L Kaufman; Ronald C Kessler; Anthony P King; William S Kremen; Bruce R Lawford; Lauren A M Lebois; Catrin Lewis; Israel Liberzon; Sarah D Linnstaedt; Bozo Lugonja; Jurjen J Luykx; Michael J Lyons; Matig R Mavissakalian; Katie A McLaughlin; Samuel A McLean; Divya Mehta; Rebecca Mellor; Charles Phillip Morris; Seid Muhie; Holly K Orcutt; Matthew Peverill; Andrew Ratanatharathorn; Victoria B Risbrough; Albert Rizzo; Andrea L Roberts; Alex O Rothbaum; Barbara O Rothbaum; Peter Roy-Byrne; Kenneth J Ruggiero; Bart P F Rutten; Dick Schijven; Julia S Seng; Christina M Sheerin; Michael A Sorenson; Martin H Teicher; Monica Uddin; Robert J Ursano; Christiaan H Vinkers; Joanne Voisey; Heike Weber; Sherry Winternitz; Miguel Xavier; Ruoting Yang; Ross McD Young; Lori A Zoellner; Rany M Salem; Richard A Shaffer; Tianying Wu; Kerry J Ressler; Murray B Stein; Karestan C Koenen
Journal:  Mol Psychiatry       Date:  2022-09-21       Impact factor: 13.437

7.  Chromosome 8p23.1 deletions as a cause of complex congenital heart defects and diaphragmatic hernia.

Authors:  Margaret J Wat; Oleg A Shchelochkov; Ashley M Holder; Amy M Breman; Aditi Dagli; Carlos Bacino; Fernando Scaglia; Roberto T Zori; Sau Wai Cheung; Daryl A Scott; Sung-Hae Lee Kang
Journal:  Am J Med Genet A       Date:  2009-08       Impact factor: 2.802

8.  Identification of candidate genes for congenital heart defects on proximal chromosome 8p.

Authors:  Tingting Li; Chunjie Liu; Yuejuan Xu; Qianqian Guo; Sun Chen; Kun Sun; Rang Xu
Journal:  Sci Rep       Date:  2016-11-03       Impact factor: 4.379

Review 9.  Partial monosomy 8p and trisomy 16q in two children with developmental delay detected by array comparative genomic hybridization.

Authors:  Zoe Papadopoulou; Ioannis Papoulidis; Stavros Sifakis; Georgios Markopoulos; Annalisa Vetro; Angeliki-Maria Vlaikou; Monica Ziegler; Thomas Liehr; Loretta Thomaidis; Orsetta Zuffardi; Maria Syrrou; Kitsos George; Emmanouil Manolakos
Journal:  Mol Med Rep       Date:  2017-10-10       Impact factor: 2.952

10.  Inherited unbalanced translocation (4p16.3p15.32 duplication/8p23.3p23.2deletion) in the four generation pedigree with intellectual disability/developmental delay.

Authors:  Dongmei Hao; Yajuan Li; Lisha Chen; Xiliang Wang; Mengxing Wang; Yuexin Yu
Journal:  Mol Cytogenet       Date:  2021-07-08       Impact factor: 2.009
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