Congenital Abnormality
|
0.100 |
Biomarker
|
group |
BEFREE |
The GREM1 is involved in the etiology of NSCL±P in the Brazilian population and reveal that the interaction between GREM1 and NTN1 may be related with the pathogenesis of this common craniofacial malformation.
|
30402937 |
2019 |
Congenital Abnormality
|
0.100 |
GeneticVariation
|
group |
BEFREE |
Nonsyndromic cleft lip with or without cleft palate (NSCL/P) is a common birth defect with a complex genetic architecture.
|
30273098 |
2019 |
Congenital Abnormality
|
0.100 |
Biomarker
|
group |
BEFREE |
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.
|
30769929 |
2019 |
Congenital Abnormality
|
0.100 |
Biomarker
|
group |
BEFREE |
Non-syndromic cleft lip, with or without cleft palate (NSCL/P), is a common craniofacial birth defect, the risk of which is influenced from multiple genetic loci.
|
31132300 |
2019 |
Congenital Abnormality
|
0.100 |
Biomarker
|
group |
BEFREE |
Nonsyndromic cleft lip with or without cleft palate (NSCL/P) is a common birth defect.
|
30848863 |
2019 |
Congenital defects
|
0.100 |
Biomarker
|
group |
BEFREE |
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.
|
30769929 |
2019 |
Dysmorphism
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
Nonsyndromic cleft lip with or without cleft palate (NSCL/P) is a common birth defect with a complex genetic architecture.
|
30273098 |
2019 |
Dysmorphism
|
0.100 |
Biomarker
|
disease |
BEFREE |
Non-syndromic cleft lip, with or without cleft palate (NSCL/P), is a common craniofacial birth defect, the risk of which is influenced from multiple genetic loci.
|
31132300 |
2019 |
Dysmorphism
|
0.100 |
Biomarker
|
disease |
BEFREE |
Nonsyndromic cleft lip with or without cleft palate (NSCL/P) is a common birth defect.
|
30848863 |
2019 |
Congenital Abnormality
|
0.100 |
Biomarker
|
group |
BEFREE |
Non-syndromic cleft lip with or without palate (NSCL/P) is a common congenital malformation worldwide, with complex etiology.
|
29211286 |
2018 |
Congenital Abnormality
|
0.100 |
Biomarker
|
group |
BEFREE |
Our observation that the impact of genetic variants on NSCL/P risk differs for males and females may further our understanding of the genetic architecture of NSCL/P and the sex differences underlying clefts and other birth defects.
|
30277614 |
2018 |
Congenital Abnormality
|
0.100 |
Biomarker
|
group |
BEFREE |
Nonsyndromic cleft lip with or without cleft palate (NSCL/P) is a birth defect for which several genes susceptibility genes been proposed.
|
29694940 |
2018 |
Congenital Abnormality
|
0.100 |
GeneticVariation
|
group |
BEFREE |
The isolated type of orofacial cleft, termed non-syndromic cleft lip with or without cleft palate (NSCL/P), is the second most common birth defect in China, with Asians having the highest incidence in the world.
|
30578914 |
2018 |
Congenital Abnormality
|
0.100 |
GeneticVariation
|
group |
BEFREE |
Non-syndromic cleft lip with or without cleft palate (NSCL/P) are the most common human congenital birth defects with a complex etiology.
|
30024657 |
2018 |
Congenital Abnormality
|
0.100 |
GeneticVariation
|
group |
BEFREE |
To understand the genetic basis of nonsyndromic cleft lip with or without cleft palate (NSCL/P) susceptibility, a complex and highly prevalent congenital malformation, we searched for genetic variants with a regulatory role in a disease-related tissue, the lip muscle (orbicularis oris muscle [OOM]), of affected individuals.
|
29053389 |
2018 |
Congenital Abnormality
|
0.100 |
GeneticVariation
|
group |
BEFREE |
Our study provided additional understanding of the genetic etiology of NSCL/P and underlined the importance of considering gene-gene interaction in the etiology of this common craniofacial malformation.
|
29341488 |
2018 |
Congenital Abnormality
|
0.100 |
Biomarker
|
group |
BEFREE |
Non-syndromic cleft lip with or without palate (NSCL/P) is one of the most common human birth defects, it results from multiple genetic and environmental risk factors.
|
30048854 |
2018 |
Congenital defects
|
0.100 |
GeneticVariation
|
group |
BEFREE |
Non-syndromic cleft lip with or without cleft palate (NSCL/P) are the most common human congenital birth defects with a complex etiology.
|
30024657 |
2018 |
Congenital defects
|
0.100 |
Biomarker
|
group |
BEFREE |
Our observation that the impact of genetic variants on NSCL/P risk differs for males and females may further our understanding of the genetic architecture of NSCL/P and the sex differences underlying clefts and other birth defects.
|
30277614 |
2018 |
Congenital defects
|
0.100 |
Biomarker
|
group |
BEFREE |
Non-syndromic cleft lip with or without palate (NSCL/P) is one of the most common human birth defects, it results from multiple genetic and environmental risk factors.
|
30048854 |
2018 |
Dysmorphism
|
0.100 |
Biomarker
|
disease |
BEFREE |
Nonsyndromic cleft lip with or without cleft palate (NSCL/P) is a birth defect for which several genes susceptibility genes been proposed.
|
29694940 |
2018 |
Dysmorphism
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
The isolated type of orofacial cleft, termed non-syndromic cleft lip with or without cleft palate (NSCL/P), is the second most common birth defect in China, with Asians having the highest incidence in the world.
|
30578914 |
2018 |
Dysmorphism
|
0.100 |
Biomarker
|
disease |
BEFREE |
Nonsyndromic cleft lip with or without cleft palate (NSCL/P) is the most common craniofacial birth defect in humans and is notable for its apparent sexual dimorphism where approximately twice as many males are affected as females.
|
30277614 |
2018 |
Congenital Abnormality
|
0.100 |
Biomarker
|
group |
BEFREE |
Nonsyndromic cleft lip with or without cleft palate (NSCL/P) is a group of common human birth defects with complex etiology.
|
28425186 |
2017 |
Congenital Abnormality
|
0.100 |
Biomarker
|
group |
BEFREE |
Nonsyndromic cleft lip with or without cleft palate (NSCL/P) is a structural craniofacial malformation featured by isolated orofacial abnormalities.
|
27734840 |
2017 |