Human chromosome 7: DNA sequence and biology

Science

Volumn 300, Issue 5620, 2003, Pages 767-772

  Scherer, Stephen W ^a,b   Cheung, Joseph ^a   MacDonald, Jeffrey R ^a   Osborne, Lucy R ^b   Nakabayashi, Kazuhiko ^a   Herbrick, Jo Anne ^a   Carson, Andrew R ^a   Parker Katiraee, Layla ^a,b   Skaug, Jennifer ^a   Khaja, Razi ^a   Zhang, Junjun ^a   Hudek, Alexander K ^a   Li, Martin ^a   Haddad, May ^a   Duggan, Gavin E ^a   Fernandez, Bridget A ^c   Kanematsu, Emiko ^a   Gentles, Simone ^a   Christopoulos, Constantine C ^a   Choufani, Sanaa ^a   Kwasnicka, Dorota ^a   Zheng, Xiangqun H ^d   Lai, Zhongwu ^d   Nusskern, Deborah ^d   Zhang, Qing ^d   Gu, Zhiping ^d   Lu, Fu ^d   Zeesman, Susan ^e   Nowaczyk, Malgorzata J ^e   Teshima, Ikuko ^a,f   Chitayat, David ^a,f   Shuman, Cheryl ^a,f   Weksberg, Rosanna ^a,f   Zackai, Elaine H ^g   Grebe, Theresa A ^h   Cox, Sarah R ^h   Kirkpatrick, Susan J ⁱ   Rahman, Nazneen ^j   Friedman, Jan M ^k   Heng, Henry H Q ^l   Pelicci, Pier Giuseppe ^m,n   Lo Coco, Francesco ^o   Belloni, Elena ^m,n   Shaffer, Lisa G ^p   Pober, Barbara ^q   Morton, Cynthia C ^r,t   Gusella, James F ^s   Bruns, Gail A P ^u   Korf, Bruce R ^s,t   Quade, Bradley J ^r   Ligon, Azra H ^r   Ferguson, Heather ^r   Higgins, Anne W ^r   Leach, Natalia T ^r   Herrick, Steven R ^r   Lemyre, Emmanuelle ^r   Farra, Chantal G ^r   Kim, Hyung Goo ^s   Summers, Anne M ^v   Gripp, Karen W ^w   Roberts, Wendy ^a   Szatmari, Peter ^e   Winsor, Elizabeth J T ^x   Grzeschik, Karl Heinz ^y   Teebi, Ahmed ^a,f   Minassian, Berge A ^a   Kere, Juha ^z   Armengol, Luis ^aa   Pujana, Miguel Angel ^aa   Estivill, Xavier ^aa   Wilson, Michael D ^ab   Koop, Ben F ^ab   Tosi, Sabrina ^ac   Moore, Gudrun E ^ad   Boright, Andrew P ^x   Zlotorynski, Eitan ^ae   Kerem, Batsheva ^ae   Kroisel, Peter M ^af   Petek, Erwin ^af   Oscier, David G ^ag   Mould, Sarah J ^ag   Döhner, Hartmut ^ah   Döhner, Konstanze ^ah   Rommens, Johanna M ^a,b   Vincent, John B ^f   Venter, J Craig ^d   Li, Peter W ^d   Mural, Richard J ^d   Adams, Mark D ^d   Tsui, Lap Chee ^a,b,ai   more..

^a HOSPITAL FOR SICK CHILDREN   (Canada)

^b UNIVERSITY OF TORONTO   (Canada)

^c MEMORIAL UNIVERSITY OF NEWFOUNDLAND   (Canada)

^d CELERA GENOMICS   (United States)

^e MCMASTER UNIVERSITY   (Canada)

^f UNIVERSITY OF TORONTO   (Canada)

^g CHILDREN S HOSPITAL OF PHILADELPHIA   (United States)

^h UNIVERSITY OF PHOENIX   (United States)

ⁱ UNIVERSITY OF WISCONSIN MADISON   (United States)

^j Section of Cancer Genetics   (United Kingdom)

^k UNIVERSITY OF BRITISH COLUMBIA   (Canada)

^l WAYNE STATE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^m EUROPEAN INSTITUTE OF ONCOLOGY   (Italy)

ⁿ FIRC INSTITUTE OF MOLECULAR ONCOLOGY   (Italy)

^o UNIVERSITY OF ROME TOR VERGATA   (Italy)

^p BAYLOR COLLEGE OF MEDICINE   (United States)

^q YALE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^r BRIGHAM AND WOMEN S HOSPITAL   (United States)

^s MASSACHUSETTS GENERAL HOSPITAL   (United States)

^t HARVARD MEDICAL SCHOOL   (United States)

^u BOSTON CHILDREN S HOSPITAL   (United States)

^v NORTH YORK GENERAL HOSPITAL   (Canada)

^w NEMOURS ALFRED I DUPONT HOSPITAL FOR CHILDREN   (United States)

^x UNIVERSITY HEALTH NETWORK   (Canada)

^y PHILIPPS UNIVERSITY MARBURG   (Germany)

^z KAROLINSKA UNIVERSITY HOSPITAL   (Sweden)

^aa CENTRE FOR GENOMIC REGULATION CRG   (Spain)

^ab UNIVERSITY OF VICTORIA   (Canada)

^ac JOHN RADCLIFFE HOSPITAL   (United Kingdom)

^ad IMPERIAL COLLEGE LONDON   (United Kingdom)

^ae HEBREW UNIVERSITY OF JERUSALEM   (Israel)

^af UNIVERSITY OF GRAZ   (Austria)

^ag ROYAL BOURNEMOUTH HOSPITAL   (United Kingdom)

^ah UNIVERSITY HOSPITAL ULM   (Germany)

^ai UNIVERSITY OF HONG KONG   (Hong Kong)

more..

Author keywords

[No Author keywords available]

Indexed keywords

DISEASES; DNA SEQUENCES; GENES;

NUCLEOTIDES;

GENETIC ENGINEERING;

NUCLEOTIDE;

CHROMOSOME; DNA;

ARTICLE; AUTISM; CHROMOSOME 7; CHROMOSOME REARRANGEMENT; DEVELOPMENTAL DISORDER; DNA SEQUENCE; GENE DUPLICATION; GENE STRUCTURE; GENOME IMPRINTING; HUMAN; MEDICAL GENETICS; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL;

ABNORMALITIES; ANIMALS; AUTISTIC DISORDER; CHROMOSOME ABERRATIONS; CHROMOSOME FRAGILE SITES; CHROMOSOME FRAGILITY; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 7; COMPUTATIONAL BIOLOGY; CPG ISLANDS; DATABASES, GENETIC; DNA, COMPLEMENTARY; EUCHROMATIN; EXPRESSED SEQUENCE TAGS; GENE DUPLICATION; GENES, OVERLAPPING; GENETIC DISEASES, INBORN; GENOMIC IMPRINTING; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; LIMB DEFORMITIES, CONGENITAL; MICE; MOLECULAR SEQUENCE DATA; MUTATION; NEOPLASMS; PSEUDOGENES; RETROELEMENTS; RNA; SEQUENCE ANALYSIS, DNA; WILLIAMS SYNDROME;

EID: 0038756128     PISSN: 00368075     EISSN: None     Source Type: Journal    
DOI: 10.1126/science.1083423     Document Type: Article

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