Clinical and molecular cytogenetic studies of a large de novo interstitial deletion 16q11.2-16q21 including the putative transcription factor gene SALL1

Journal of Medical Genetics

Volumn 37, Issue 5, 2000, Pages 389-392

  Knoblauch, H ^a   Thiel, G ^a   Tinschert, S ^a   Korner, H ^a   Tennstedt, C ^a   Chaoui, R ^a   Kohlhase, J ^a   Dixkens, C ^a   Blanck, C ^a  

^a CHARITÉ UNIVERSITÄTSMEDIZIN BERLIN   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

TRANSCRIPTION FACTOR;

CASE REPORT; CHROMOSOME 16Q; FETUS; FETUS MALFORMATION; GENE DELETION; HUMAN; LETTER; MALE; PHENOTYPE; PRIORITY JOURNAL;

EID: 0034102933     PISSN: 00222593     EISSN: None     Source Type: Journal    
DOI: 10.1136/jmg.37.5.389     Document Type: Letter

References (51)