Microdeletion on 17p11.2 in a Smith-Magenis syndrome patient with mental retardation and congenital heart defect: first report from China.

Genetics and molecular research : GMR

Volumn 11, Issue 3, 2012, Pages 2321-2327

  Huang, C ^a   Yang, Y F ^b   Zhang, H ^b   Xie, L ^b   Chen, J L ^b   Wang, J ^b   Tan, Z P ^b   Luo, H ^b  

^a CENTRAL SOUTH UNIVERSITY   (China)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CASE REPORT; CHILD; CHINA; CHROMOSOME 17; CHROMOSOME DELETION; CONGENITAL HEART MALFORMATION; FACIES; FEMALE; GENETICS; HUMAN; INTELLECTUAL IMPAIRMENT; NEWBORN; PRESCHOOL CHILD; SINGLE NUCLEOTIDE POLYMORPHISM; SMITH MAGENIS SYNDROME;

CHILD; CHILD, PRESCHOOL; CHINA; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 17; FACIES; FEMALE; HEART DEFECTS, CONGENITAL; HUMANS; INFANT, NEWBORN; INTELLECTUAL DISABILITY; POLYMORPHISM, SINGLE NUCLEOTIDE; SMITH-MAGENIS SYNDROME;

EID: 84871866760     PISSN: None     EISSN: 16765680     Source Type: Journal    
DOI: 10.4238/2012.August.13.5     Document Type: Article

References (0)