Construction of a 1.2-Mb sequence-ready contig of chromosome 11q13 encompassing the multiple endocrine neoplasia type 1 (MEN1) gene

Genomics

Volumn 44, Issue 1, 1997, Pages 94-100

  Lemmens, Irma ^a   Merregaert, Jozef ^b   Van De Ven, Wim J M ^a   Koen, Kas ^a   Zhang, Chang X ^c,d   Giraud, Sophie ^c   Wautot, Virginie ^d   Buisson, Nathalie ^c,d   De Witte, Ko ^d   Salandre, Janine ^c   Lenoir, Gilbert ^c,d   Calender, Alain ^c,d   Parente, Fabienne ^e   Quincey, Danielle ^e   Courseaux, Anouk ^e   Carle, George F ^e   Gaudray, Patrick ^e   De Wit, Mireille J ^f   Lips, Cornelis J M ^f   Höppener, Jo W M ^f   Khodaei, Shideh ^g   Grant, Abby L ^g   Weber, Günther ^g   Kytölä, Soili ^g,h   Teh, Bin T ^g   Farnebo, Filip ^g   Grimmond, Sean ⁱ   Phelan, Catherine ^g   Larsson, Catharina ^g   Forbes, Simon A ^j   Bassett, J H Duncan ^j   Pannett, Anna A J ^j   Thakker, Rajesh V ^j   more..

^a UNIVERSITY OF LEUVEN   (Belgium)

^b UNIVERSITY OF ANTWERP   (Belgium)

^c EDOUARD HERRIOT HOSPITAL   (France)

^d UNIVERSITÉ LYON 1   (France)

^e CNRS   (France)

^f UNIVERSITY MEDICAL CENTER UTRECHT   (Netherlands)

^g KAROLINSKA UNIVERSITY HOSPITAL   (Sweden)

^h OULU UNIVERSITY HOSPITAL   (Finland)

ⁱ QIMR BERGHOFER MEDICAL RESEARCH INSTITUTE   (Australia)

^j MRC CLINICAL SCIENCES CENTRE   (United Kingdom)

more..

Author keywords

[No Author keywords available]

Indexed keywords

CONTIG;

ARTICLE; AUTOSOMAL DOMINANT DISORDER; CHROMOSOMAL LOCALIZATION; CHROMOSOME 11Q; CHROMOSOME MAP; COSMID; DNA POLYMORPHISM; FAMILIAL CANCER; FLUORESCENCE IN SITU HYBRIDIZATION; GENE CLUSTER; GENE LOCUS; HUMAN; HUMAN CELL; HYPOPHYSIS TUMOR; MULTIPLE ENDOCRINE NEOPLASIA; PANCREAS TUMOR; PARATHYROID TUMOR; PRIORITY JOURNAL; SEQUENCE ANALYSIS;

EID: 0031571636     PISSN: 08887543     EISSN: None     Source Type: Journal    
DOI: 10.1006/geno.1997.4872     Document Type: Article

References (33)

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