Association between NOGGIN and SPRY2 polymorphisms and nonsyndromic cleft lip with or without cleft palate

American Journal of Medical Genetics, Part A

Volumn 167, Issue 1, 2015, Pages 137-141

  Song, Tao ^a   Shi, Jinna ^a   Guo, Qiang ^a   Lv, Kewen ^a   Jiao, Xiaohui ^a   Hu, Tenglong ^a   Sun, Xiangyu ^a   Fu, Songbin ^a  

^a HARBIN MEDICAL UNIVERSITY   (China)

Author keywords

NOG; Nonsyndromic cleft lip with or without cleft palate (NSCLP); SNPs; SPRY2

Indexed keywords

ADOLESCENT; ADULT; AGED; ARTICLE; CHILD; CHINA; CHINESE; CONTROLLED STUDY; FEMALE; GENE FREQUENCY; GENETIC ASSOCIATION; GENETIC RISK; GENETIC SUSCEPTIBILITY; GENOTYPE; HOMOZYGOTE; HUMAN; LIP MALFORMATION; MAJOR CLINICAL STUDY; MALE; MULTIFACTORIAL GENETIC DISORDER; NOGGIN GENE; NONSYNDROMIC CLEFT LIP WITH OR WITHOUT CLEFT PALATE; PALATE MALFORMATION; PRIORITY JOURNAL; RISK REDUCTION; SINGLE NUCLEOTIDE POLYMORPHISM; SPRY2 GENE; ALLELE; CASE CONTROL STUDY; CLEFT LIP; CLEFT PALATE; COMPLICATION; GENETIC PREDISPOSITION; GENETICS; HAPLOTYPE; INFANT; PRESCHOOL CHILD; RISK; YOUNG ADULT;

CARRIER PROTEIN; MEMBRANE PROTEIN; NOGGIN PROTEIN; SIGNAL PEPTIDE; SPRY2 PROTEIN, HUMAN;

ADOLESCENT; ADULT; ALLELES; CARRIER PROTEINS; CASE-CONTROL STUDIES; CHILD; CHILD, PRESCHOOL; CLEFT LIP; CLEFT PALATE; FEMALE; GENETIC ASSOCIATION STUDIES; GENETIC PREDISPOSITION TO DISEASE; HAPLOTYPES; HUMANS; INFANT; INTRACELLULAR SIGNALING PEPTIDES AND PROTEINS; MALE; MEMBRANE PROTEINS; ODDS RATIO; POLYMORPHISM, SINGLE NUCLEOTIDE; YOUNG ADULT;

EID: 84919684536     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.36802     Document Type: Article

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