Polyalanine expansion in synpolydactyly might result from unequal crossing-over of HOXD13

Science

Volumn 275, Issue 5298, 1997, Pages 408-409

  Van Cappellen, P ^a   Ingall, E D ^a   Warren, S T ^a   Muragaki, Y ^a   Mundlos, S ^a   Upton, J ^a   Olsen, B R ^a  

^a EMORY UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ALANINE; MUTANT PROTEIN;

AMINO ACID SEQUENCE; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CROSSING OVER; GENETIC DISORDER; HUMAN; LIMB MALFORMATION; NUCLEOTIDE SEQUENCE; POLYDACTYLY; PRIORITY JOURNAL; SYNDACTYLY;

ALLELES; AMINO ACID SEQUENCE; BASE SEQUENCE; CROSSING OVER, GENETIC; HOMEODOMAIN PROTEINS; HUMANS; MOLECULAR SEQUENCE DATA; MUTATION; PEPTIDES; POLYDACTYLY; SYNDACTYLY; TRANSCRIPTION FACTORS; TRINUCLEOTIDE REPEATS;

EID: 0031015410     PISSN: 00368075     EISSN: None     Source Type: Journal    
DOI: 10.1126/science.275.5298.408     Document Type: Article

References (7)