About: Benign familial neonatal convulsions linked to genetic markers on chromosome 20.

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About: Benign familial neonatal convulsions linked to genetic markers on chromosome 20. Goto Sponge NotDistinct Permalink

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scientific article published in February 1989

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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) 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) 1989 nî lūn-bûn (nan) 1989年の論文 (ja) 1989년 논문 (ko) artículo científico publicado en 1989 (es) artículu científicu espublizáu en 1989 (ast) 1989年学术文章 (zh-cn) 1989年学术文章 (zh-sg) 1989年学术文章 (zh-hans) 1989年学术文章 (wuu) 1989年学术文章 (zh-my) 1989年學術文章 (zh-hk) 1989年學術文章 (zh-tw) 1989年學術文章 (zh-hant) 1989年學術文章 (yue) 1989年學術文章 (zh-mo) наукова стаття, опублікована в лютому 1989 (uk) scientific article published in February 1989 (en-ca) scientific article published in February 1989 (en-gb) 1989年学术文章 (zh) scientific article published in February 1989 (en) مقالة علمية نشرت في فبراير 1989 (ar) ফেব্রুয়ারি ১৯৮৯-এ প্রকাশিত বৈজ্ঞানিক নিবন্ধ (bn) գիտական հոդված հրատարակված 1989 թվականի փետրվարին (hy)
publication date	wds:Q44109661-D6E80D2A-DBAD-4C5E-8973-10E3A0D0BDE1
publication date	1989-02-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q44109661-992CE662-C631-4C51-96B6-83743C9168C6
language of work or name	English
exact match	wds:Q44109661-4C08F71B-F078-4FD4-96A2-193570179D42
exact match	https://scigraph.springernature.com/pub.10.1038/337647a0
cites work	wds:Q44109661-073DBD7A-E006-48B4-9CAE-E23B4547F8E8 wds:Q44109661-2AD77082-2C10-4F1C-8621-26ABB015370E wds:Q44109661-325BD432-AF24-4949-B050-1758180BEDB2 wds:Q44109661-37962D9E-0B80-41E9-A305-8BECE3A18770 wds:Q44109661-4C5CD2E8-0CEC-490B-BDA5-EE56D4C0A431 wds:Q44109661-4E7FD4B0-1238-4B4D-BE83-43E2D2DFCEF1 wds:Q44109661-6A54A721-E76C-422D-ABF3-0A0712062E55 wds:Q44109661-6F9FD91E-E506-4A7B-BD02-67013C0035B7 wds:Q44109661-789EB058-8C5D-4D62-810E-80599FD1227C wds:Q44109661-7D7DB92B-681B-4777-B716-B7F26924A1DE wds:Q44109661-C75CE330-E591-4208-9807-5CE61357EA94 wds:Q44109661-D6AA7730-9E0C-4638-92D5-04A25FF6967C wds:Q44109661-E879041E-FB7D-4192-9D1C-952E94125B53 wds:Q44109661-EF9BDE13-BD8A-4E57-9539-FB71CB10AD27 wds:Q44109661-F2E7067D-5ED2-4F85-9B10-7D3528CEA203 wds:Q44109661-F8EB2650-0B93-4319-BDC8-B2DD77AF759D
cites work	Restriction sites containing CpG show a higher frequency of polymorphism in human DNA Report of the Committee on Methods of Linkage Analysis and Reporting Construction of linkage maps with DNA markers for human chromosomes. Benign familial neonatal convulsions Benign familial convulsions in the neonatal period and early infancy Benign familial neonatal seizures Localization and linkage of three polymorphic DNA sequences on human chromosome 20 Benign familial neonatal seizures: clinical and electroencephalographic characteristics Benign familial neonatal convulsions. Isolation and mapping of a polymorphic DNA sequence (pCMM6) on chromosome 20 [D20S19] Isolation and mapping of a polymorphic DNA sequence (pRMR6) on chromosome 20 [D20S20] Benign familial neonatal convulsions Familial neonatal and infantile seizures: an autosomal-dominant disorder Autosomal dominant benign neonatal seizures Benign familial neonatal convulsions Benign convulsions in infancy
author name string	wds:Q44109661-14603346-CFBD-45D7-914B-6F88BEF384F2 wds:Q44109661-2F4C35AE-CD73-4DE0-8229-0015B151AF7C

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