Molecular-evolutionary mechanisms for genomic disorders

Current Opinion in Genetics and Development

Volumn 12, Issue 3, 2002, Pages 312-319

  Stankiewicz, Pawel ^a   Lupski, James R ^a  

^a TEXAS CHILDREN S HOSPITAL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DNA; MYELIN PROTEIN; PMP22 PROTEIN, HUMAN;

BIOAVAILABILITY; CARCINOGENESIS; GENE REARRANGEMENT; GENETIC DISORDER; GENOME; HUMAN; KARYOTYPE; MOLECULAR EVOLUTION; MOLECULAR SIZE; NONHUMAN; PRIMATE; PRIORITY JOURNAL; REGULATORY MECHANISM; REVIEW; SEQUENCE HOMOLOGY; ANIMAL; GENE CONVERSION; GENE DELETION; GENETIC RECOMBINATION; GENETICS; HEREDITARY MOTOR SENSORY NEUROPATHY; NUCLEOTIDE REPEAT; WILLIAMS BEUREN SYNDROME;

PRIMATES;

ANIMALS; CHARCOT-MARIE-TOOTH DISEASE; EVOLUTION, MOLECULAR; GENE CONVERSION; GENETIC DISEASES, INBORN; HUMANS; MYELIN PROTEINS; RECOMBINATION, GENETIC; REPETITIVE SEQUENCES, NUCLEIC ACID; SEQUENCE DELETION; WILLIAMS SYNDROME;

EID: 0036591666     PISSN: 0959437X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0959-437X(02)00304-0     Document Type: Review

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