Bohring syndrome [3]

American Journal of Medical Genetics

Volumn 92, Issue 5, 2000, Pages 366-368

  Brunner, H G ^a   Van Tintelen, J P ^b   De Boer, R J ^c  

^a RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

^b UNIVERSITY MEDICAL CENTER GRONINGEN   (Netherlands)

^c RIJNSTATE HOSPITAL   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

BOHRING OPITZ SYNDROME; CASE REPORT; CHROMOSOME 12P; DIAGNOSTIC VALUE; DISEASE CLASSIFICATION; FACE MALFORMATION; FEMALE; HUMAN; HUMAN CELL; HUMAN TISSUE; LETTER; NEWBORN; PRIORITY JOURNAL; SCORING SYSTEM; SYNDROME DELINEATION; TETRASOMY; MULTIPLE MALFORMATION SYNDROME; NOTE; PATHOLOGY; SYNDROME;

ABNORMALITIES, MULTIPLE; FEMALE; HUMANS; INFANT, NEWBORN; SYNDROME;

EID: 0034686549     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/1096-8628(20000619)92:5<366::AID-AJMG15>3.0.CO;2-U     Document Type: Letter

References (2)