About: Emerin deletion reveals a common X-chromosome inversion mediated by inverted repeats.

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About: Emerin deletion reveals a common X-chromosome inversion mediated by inverted repeats. Goto Sponge NotDistinct Permalink

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scientific article published in May 1997

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rdf:type	Item
description	videnskabelig artikel (da) article científic (ca) article scientific (oc) articol științific (ro) articolo scientifico (it) artigo científico (gl) artigo científico (pt) artigo científico (pt-br) artikull shkencor (sq) artikulong pang-agham (tl) artykuł naukowy (pl) artículu científicu (ast) bilimsel makale (tr) scienca artikolo (eo) teaduslik artikkel (et) tieteellinen artikkeli (fi) tudományos cikk (hu) vedecký článok (sk) vetenskaplig artikel (sv) vitenskapelig artikkel (nb) vitskapeleg artikkel (nn) vědecký článek (cs) wetenschappelijk artikel (nl) wissenschaftlicher Artikel (de) επιστημονικό άρθρο (el) научна статия (bg) научная статья (ru) научни чланак (sr) מאמר מדעי (he) სამეცნიერო სტატია (ka) บทความทางวิทยาศาสตร์ (th) artikel ilmiah (id) bài báo khoa học (vi) naučni članak (sr-el) мақолаи илмӣ (tg-cyrl) научни чланак (sr-ec) article scientifique (fr) 1997 nî lūn-bûn (nan) 1997年の論文 (ja) 1997년 논문 (ko) artículo científico publicado en 1997 (es) 1997年学术文章 (zh-cn) 1997年学术文章 (zh-sg) 1997年学术文章 (zh-hans) 1997年学术文章 (wuu) 1997年学术文章 (zh-my) 1997年學術文章 (zh-hk) 1997年學術文章 (zh-tw) 1997年學術文章 (zh-hant) 1997年學術文章 (yue) 1997年學術文章 (zh-mo) наукова стаття, опублікована в травні 1997 (uk) scientific article published in May 1997 (en-ca) scientific article published in May 1997 (en-gb) 1997年学术文章 (zh) مقالة علمية نشرت في مايو 1997 (ar) মে ১৯৯৭-এ প্রকাশিত বৈজ্ঞানিক নিবন্ধ (bn) scientific article published in May 1997 (en)
publication date	wds:Q48050604-78FE2EE8-AB50-47E3-B5A5-541005EE7431
publication date	1997-05-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q48050604-CF92555C-79AC-4592-A51C-65ADF07A3729
language of work or name	English
exact match	wds:Q48050604-D129870D-1874-4E37-94A5-947BE3582E05
exact match	https://scigraph.springernature.com/pub.10.1038/ng0597-96
cites work	wds:Q48050604-074EF237-7B0F-4D6D-8A55-3A9DE39CD149 wds:Q48050604-1047E08C-B0FD-474E-AF03-440F0DBD3CB1 wds:Q48050604-10B37A61-E3F9-4414-818F-0CB1DE170D09 wds:Q48050604-12DE03EF-B511-4FB5-8172-8039109086EA wds:Q48050604-1B7CEFC8-5285-4FD2-9139-42B3CCCC34D5 wds:Q48050604-40CECA47-687B-433D-9539-8DAF051C54C5 wds:Q48050604-6C6E164A-1DE2-4C66-BC94-35E424F02DA4 wds:Q48050604-6D108C37-107E-408C-B81F-35CFB4A27974 wds:Q48050604-7101D010-0B4E-4FCC-8A4E-3843DA15A661 wds:Q48050604-8666B426-9427-45D4-B0CA-40AA519EE720 wds:Q48050604-9081A13D-A961-4382-9B86-C4D5BEAFE05D wds:Q48050604-9B927E71-74E5-4C31-8FAF-F2E3D45D5212 wds:Q48050604-A14FCE12-029B-4CDC-B6B3-61C9441C971A wds:Q48050604-A955DC7A-6A6A-4045-92B0-DD015055CFB1 wds:Q48050604-C9FF5BCF-6C9B-4AC4-86C5-EA955145A145 wds:Q48050604-DA3FBCE5-2E3C-4A8C-9784-055E6DF85E11 wds:Q48050604-EA02A26E-CFBE-43C0-B4AE-07BE02585EB6 wds:Q48050604-EF0FBE2F-6828-436F-A0AC-79DDDE827304 wds:Q48050604-F1A7C797-04F5-429A-AD7B-AC611AA6E843 wds:Q48050604-F3904598-0B46-46F0-AC87-A8D01E949148 wds:Q48050604-FC3D64A5-5E6D-4C80-AA70-814304940015
cites work	Factor VIII gene inversions causing severe hemophilia A originate almost exclusively in male germ cells G6PD haplotypes spanning Xq28 from F8C to red/green color vision Identification of a novel X-linked gene responsible for Emery-Dreifuss muscular dystrophy Emery-Dreifuss syndrome Actin-binding protein requirement for cortical stability and efficient locomotion A muscle-specific DNase I-like gene in human Xq28. Mechanisms of nonhomologous recombination in mammalian cells Inversions disrupting the factor VIII gene are a common cause of severe haemophilia A Charcot-Marie-Tooth type 1A duplication appears to arise from recombination at repeat sequences flanking the 1.5 Mb monomer unit Integration of gene maps: chromosome X Actin-binding protein (ABP-280) filamin gene (FLN) maps telomeric to the color vision locus (R/GCP) and centromeric to G6PD in Xq28. Centre d'etude du polymorphisme humain (CEPH): collaborative genetic mapping of the human genome Long-range sequence analysis in Xq28: thirteen known and six candidate genes in 219.4 kb of high GC DNA between the RCP/GCP and G6PD loci Investigation of the factor VIII intron 22 repeated region (int22h) and the associated inversion junctions

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