Non-syndromic cleft lip with or without cleft palate (NSCL/P) is one of common birth defects in China, with genetic and environmental components contributing to the etiology. Genome wide association studies (GWASs) have identified SPRY1 and SPRY2 to be associated with NSCL/P among Chinese populations. This study aimed to further explore potential genetic effect and gene—environment interaction among SPRY genes based on haplotype analysis, using 806 Chinese case—parent NSCL/P trios drawn from an international consortium which conducted a genome-wide association study. After the process of quality control, 190 single nucleotide polymorphisms (SNPs) of SPRY genes were included for analyses. Haplotype and haplotype—environment...
Nonsyndromic cleft palate (CP) is a common birth defect with a complex and heterogeneous etiology in...
Nonsyndromic cleft lip with or without cleft palate (NSCL/P), the most common type of orofacial clef...
Nonsyndromic cleft palate (CP) is a common birth defect with a complex and heterogeneous etiology in...
Non-syndromic cleft lip with or without cleft palate (NSCL/P) is a common birth defect with a comple...
To explore the association between 18 candidate genes encoding enzymes on the folate/homocysteine me...
This study examined the association between 49 markers in the Runt-related transcription factor 2 (R...
Nonsyndromic cleft palate (CP) is one of the most common human birth defects and both genetic and en...
Nonsyndromic cleft palate (CP) is one of the most common human birth defects and both genetic and en...
Background: Non-syndromic cleft lip with or without cleft palate (NSCL/P) is a common disorder with ...
Objectives To identify the loci involved in nonsyndromic cleft lip with or without cleft palate (NSC...
Non-syndromic cleft lip with or without cleft palate (NSCL/P) is a common disorder with complex etio...
Nonsyndromic cleft palate (CP) is one of the most common human birth defects and both genetic and en...
<div><p>Nonsyndromic cleft palate (CP) is one of the most common human birth defects and both geneti...
Nonsyndromic cleft palate (CP) is one of the most common human birth defects and both genetic and en...
Although multiple genes have been identified as genetic risk factors for isolated, non-syndromic cle...
Nonsyndromic cleft palate (CP) is a common birth defect with a complex and heterogeneous etiology in...
Nonsyndromic cleft lip with or without cleft palate (NSCL/P), the most common type of orofacial clef...
Nonsyndromic cleft palate (CP) is a common birth defect with a complex and heterogeneous etiology in...
Non-syndromic cleft lip with or without cleft palate (NSCL/P) is a common birth defect with a comple...
To explore the association between 18 candidate genes encoding enzymes on the folate/homocysteine me...
This study examined the association between 49 markers in the Runt-related transcription factor 2 (R...
Nonsyndromic cleft palate (CP) is one of the most common human birth defects and both genetic and en...
Nonsyndromic cleft palate (CP) is one of the most common human birth defects and both genetic and en...
Background: Non-syndromic cleft lip with or without cleft palate (NSCL/P) is a common disorder with ...
Objectives To identify the loci involved in nonsyndromic cleft lip with or without cleft palate (NSC...
Non-syndromic cleft lip with or without cleft palate (NSCL/P) is a common disorder with complex etio...
Nonsyndromic cleft palate (CP) is one of the most common human birth defects and both genetic and en...
<div><p>Nonsyndromic cleft palate (CP) is one of the most common human birth defects and both geneti...
Nonsyndromic cleft palate (CP) is one of the most common human birth defects and both genetic and en...
Although multiple genes have been identified as genetic risk factors for isolated, non-syndromic cle...
Nonsyndromic cleft palate (CP) is a common birth defect with a complex and heterogeneous etiology in...
Nonsyndromic cleft lip with or without cleft palate (NSCL/P), the most common type of orofacial clef...
Nonsyndromic cleft palate (CP) is a common birth defect with a complex and heterogeneous etiology in...