Exclusion of a disease relevant role of PAX4 in the aetiology of Silver-Russell syndrome: screening for mutations and determination of imprinting status.

Journal of medical genetics

Volumn 37, Issue 12, 2000, Pages

  Mergenthaler, S ^a   Eggermann, K ^a   Tomiuk, J ^a   Ranke, M B ^a   Wollmann, H A ^a   Eggermann, T ^a  

^a NONE

Author keywords

[No Author keywords available]

Indexed keywords

HOMEODOMAIN PROTEIN; PAIRED BOX TRANSCRIPTION FACTOR; PAX4 PROTEIN, HUMAN; REPRESSOR PROTEIN; TRANSCRIPTION FACTOR;

GENETICS; GENOME IMPRINTING; HUMAN; INTRAUTERINE GROWTH RETARDATION; LETTER; MALE; MULTIPLE MALFORMATION SYNDROME; MUTATION; SYNDROME;

ABNORMALITIES, MULTIPLE; FETAL GROWTH RETARDATION; GENOMIC IMPRINTING; HOMEODOMAIN PROTEINS; HUMANS; MALE; MUTATION; PAIRED BOX TRANSCRIPTION FACTORS; REPRESSOR PROTEINS; SYNDROME; TRANSCRIPTION FACTORS;

MLCS; MLOWN;

EID: 0034546652     PISSN: None     EISSN: 14686244     Source Type: Journal    
DOI: 10.1136/jmg.37.12.e44     Document Type: Letter

References (0)