Art

J-GLOBAL ID：200902153599329717   Reference number：00A0678694

Sequence-based Structural Features between Kvlqt1 and Tapa1 on Mouse Chromosome 7F4/F5 Corresponding to the Beckwith-Wiedemann Syndrome Region on Human 11p15.5: long-stretches of Unusually Well Conserved Intronic Sequences of Kvlqt1 between Mouse and Human.

ヒト11p15.5上のBeckwith-Wiedmann症候群領域に相当するマウス染色体7F4/F5上のKvlqt1とTapa1間の配列に基づく構造特性

Author (9)： YATSUKI H (Saga Medical School, Saga, JPN) ,  WATANABE H (RIKEN Genomic Sci. Center(GSC), Kanagawa, JPN) ,  HATTORI M (RIKEN Genomic Sci. Center(GSC), Kanagawa, JPN) ,  JOH K (Saga Medical School, Saga, JPN) ,  SOEJIMA H (Saga Medical School, Saga, JPN) ,  KOMODA H (Saga Medical School, Saga, JPN) ,  XIN Z (Saga Medical School, Saga, JPN) ,  SASAKI H (National Inst. Genetics, Shizuoka, JPN) ,  MUKAI T (Saga Medical School, Saga, JPN)
Material： DNA Research  (DNA Res)
Volume： 7  Issue： 3  Page： 195-206  Publication year： Jun. 30, 2000 
JST Material Number： L2015A  ISSN： 1340-2838  Document type： Article
Article type： 原著論文  Country of issue： Japan (JPN)  Language： ENGLISH (EN)

Thesaurus term： *abnormality ,...
Semi thesaurus term： Beckwith-Wiedemann syndrome ,...

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JST classification (2)： Structure and chemistry of genes  (EC02020U) ,  Congenital diseases,deformities in general.  (GD03010V)

Terms in the title (3)： ヒト ,  マウス ,  構造特性