Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome

Cell

Volumn 65, Issue 5, 1991, Pages 905-914

  Verkerk, Annemiske J M H ^a   Pieretti, Maura ^b   Sutcliffe, James S ^b   Fu, Ying Hui ^b   Kuhl, Derek P A ^b   Pizzuti, Antonio ^b   Reiner, Orly ^b   Richards, Stephen ^b   Victoria, Maureen F ^b   Zhang, Fuping ^c   Eussen, Bert E ^a   van Ommen, Gert Jan B ^d   Blonden, Lau A J ^d   Riggins, Gregory J ^b   Chastain, Jane L ^c   Kunst, Catherine B ^a   Galjaard, Hans ^a   Thomas Caskey, C ^b   Nelson, David L ^b   Oostra, Ben A ^e   Warran, Stephen T ^c   more..

^a ERASMUS UNIVERSITY ROTTERDAM   (Netherlands)

^b HOWARD HUGHES MEDICAL INSTITUTE   (United States)

^c EMORY UNIVERSITY SCHOOL OF MEDICINE   (United States)

^d LEIDEN UNIVERSITY   (Netherlands)

^e ERASMUS MEDICAL CENTER   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; BRAIN; DNA METHYLATION; DNA SEQUENCE; FETUS; FRAGILE X SYNDROME; GENE STRUCTURE; HUMAN; HUMAN TISSUE; NONHUMAN; PRIORITY JOURNAL; YEAST ARTIFICIAL CHROMOSOME;

ALLELES; AMINO ACID SEQUENCE; BASE SEQUENCE; BLOTTING, NORTHERN; BRAIN; COSMIDS; DNA; EXONS; FRAGILE X SYNDROME; GENE LIBRARY; GENE REARRANGEMENT; HUMAN; MOLECULAR SEQUENCE DATA; NERVE TISSUE PROTEINS; OLIGONUCLEOTIDE PROBES; POLYMERASE CHAIN REACTION; RECOMBINATION, GENETIC; REPETITIVE SEQUENCES, NUCLEIC ACID; RESTRICTION MAPPING; RNA; SUPPORT, NON-U.S. GOV'T; SUPPORT, U.S. GOV'T, NON-P.H.S.; SUPPORT, U.S. GOV'T, P.H.S.; TRANSLOCATION (GENETICS); VARIATION (GENETICS); X CHROMOSOME;

EID: 0025905795     PISSN: 00928674     EISSN: None     Source Type: Journal    
DOI: 10.1016/0092-8674(91)90397-H     Document Type: Article

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