|
Volumn 50, Issue 8, 2012, Pages 606-611
|
[Cornelia de Lange syndrome: report of a case and the review of literature on 17 cases].
|
Author keywords
[No Author keywords available]
|
Indexed keywords
NIPBL PROTEIN, HUMAN;
PROTEIN;
CASE REPORT;
CAUSE OF DEATH;
CHILD;
CRANIOFACIAL MALFORMATION;
DE LANGE SYNDROME;
FEMALE;
GENETIC SCREENING;
GENETICS;
HUMAN;
INFANT;
INTELLECTUAL IMPAIRMENT;
MALE;
MULTIPLE MALFORMATION SYNDROME;
MUTATION;
NEWBORN;
NUCLEAR MAGNETIC RESONANCE IMAGING;
PATENT DUCTUS ARTERIOSUS;
PATHOLOGY;
PRESCHOOL CHILD;
REVIEW;
SEVERITY OF ILLNESS INDEX;
ABNORMALITIES, MULTIPLE;
CAUSE OF DEATH;
CHILD;
CHILD, PRESCHOOL;
CRANIOFACIAL ABNORMALITIES;
DE LANGE SYNDROME;
DUCTUS ARTERIOSUS, PATENT;
FEMALE;
GENETIC TESTING;
HUMANS;
INFANT;
INFANT, NEWBORN;
INTELLECTUAL DISABILITY;
MAGNETIC RESONANCE IMAGING;
MALE;
MUTATION;
PROTEINS;
SEVERITY OF ILLNESS INDEX;
|
EID: 84874959757
PISSN: 05781310
EISSN: None
Source Type: Journal
DOI: None Document Type: Review |
Times cited : (8)
|
References (0)
|