Mutation analysis of H19 and NAP1L4 (hNAP2) candidate genes and IGF2 DMR2 in Beckwith-Wiedemann syndrome

Journal of Medical Genetics

Volumn 37, Issue 3, 2000, Pages 212-215

  Catchpoole, D ^a   Smallwood, A V ^a   Joyce, J A ^a   Murrell, A ^a   Lam, W ^a   Tang, T ^a   Munroe, D ^a   Reik, W ^a   Schofield, P N ^a   Maher, E R ^a  

^a UNIVERSITY OF BIRMINGHAM   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

SOMATOMEDIN B;

BECKWITH WIEDEMANN SYNDROME; FEMALE; GENE MAPPING; GENE MUTATION; GENOME IMPRINTING; HUMAN; LETTER; MALE; METHYLATION; PRIORITY JOURNAL;

EID: 0034056510     PISSN: 00222593     EISSN: None     Source Type: Journal    
DOI: 10.1136/jmg.37.3.212     Document Type: Letter

References (36)