Evidence for a new microdeletion syndrome in 15q21.

International journal of molecular medicine

Volumn 11, Issue 5, 2003, Pages 575-577

  Liehr, T ^a   Starke, H ^a   Heller, A ^a   Weise, A ^a   Beensen, V ^a   Senger, G ^a   Kittner, G ^a   Prechtel, M ^a   Claussen, U ^a   Seidel, J ^a  

^a Institut fur Humangenetik und Anthropologie   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CASE REPORT; CHROMOSOME 15; CHROMOSOME DELETION; CRANIOFACIAL MALFORMATION; FEMALE; GENETICS; GROWTH DISORDER; HUMAN; INFANT; MENTAL DEFICIENCY; MULTIPLE MALFORMATION SYNDROME; SYNDROME;

ABNORMALITIES, MULTIPLE; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 15; CRANIOFACIAL ABNORMALITIES; FEMALE; GROWTH DISORDERS; HUMANS; INFANT; MENTAL RETARDATION; SYNDROME;

MLCS; MLOWN;

EID: 0642286405     PISSN: 11073756     EISSN: None     Source Type: Journal    
DOI: 10.3892/ijmm.11.5.575     Document Type: Article

References (0)