Correlation between CTG trinucleotide repeat length and frequency of severe congenital myotonic dystrophy

Nature Genetics

Volumn 1, Issue 3, 1992, Pages 192-195

  Tsilfidis, Catherine ^a   MacKenzie, Alex E ^a,b   Mettler, Gabrielle ^b   Barceló, Juana ^a   Korneluk, Robert G ^a,b  

^a UNIVERSITY OF OTTAWA   (Canada)

^b CHILDREN S HOSPITAL OF EASTERN ONTARIO   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

DNA;

ARTICLE; FEMALE; GENE AMPLIFICATION; GENE LINKAGE DISEQUILIBRIUM; GENETIC POLYMORPHISM; GENETICS; HUMAN; MALE; MYOTONIC DYSTROPHY; NEWBORN; NUCLEOTIDE REPEAT; NUCLEOTIDE SEQUENCE; PREGNANCY;

BASE SEQUENCE; DNA; FEMALE; GENE AMPLIFICATION; HUMAN; INFANT, NEWBORN; LINKAGE DISEQUILIBRIUM; MALE; MYOTONIC DYSTROPHY; POLYMORPHISM (GENETICS); PREGNANCY; REPETITIVE SEQUENCES, NUCLEIC ACID; SUPPORT, NON-U.S. GOV'T;

EID: 0026879229     PISSN: 10614036     EISSN: 15461718     Source Type: Journal    
DOI: 10.1038/ng0692-192     Document Type: Article

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