Objective: To determine the frequency of the transforming growth factor-alpha (TGFα) Taq1 polymorphism in nonsyndromic cleft lip with or without cleft palate (CL±P) and cleft palate only (CP) in Kelantan, Malaysia. Setting: The study was conducted at the Combined Cleft Clinic and at the Human Genome Centre in Hospital Universiti Sains Malaysia in Kelantan, Malaysia. Design: We examined the C2/Taq1 variant of the TGFα gene in 46 patients with nonsyndromic CL±P or CP only and in 33 controls. The TGFα genotype frequencies in patients were compared with those in controls using the chisquare or Fisher exact test. DNA samples were obtained from peripheral blood. Results: No association was found between TGFαTaq1 polymorphism and CL±P or CP in thi...
Background: Cleft lip and palate are congenital disorders which induce affected individuals med...
Objective: To assess the possible association between TGFB3 allele variants and nonsyndromic cleft l...
OBJECTIVE: Orofacial clefts (OFCs) are one of the most common birth defects in humans. They are the...
Objectives: Orofacial clefts are major human birth defects with complex etiology. Previous studies h...
Context: Non Syndromic Cleft lip/Palate is a congenital anomaly with significant medical, psychologi...
We performed ameta-analysis of the association of transforming growth factor α gene (TGFA) polymorph...
OBJECTIVES: Nonsyndromic cleft lip with or without cleft palate (CL/P) is a frequent craniofacial ma...
 Objective: This study aimed to detect and analyze transforming growth factor alpha (TGFA) BamHI an...
Background: Genetic studies have demonstrated that non-syndromic cleft is composed of two separate e...
Cleft lip with or without cleft palate and cleft palate alone are the most common craniofacial anom...
Genetic studies have demonstrated that nonsyndromic cleft is composed of two separate entities: the ...
Introduction: Non-syndromic cleft lip with or without cleft palate (NCL±P) is characterized by a mul...
Background - Cleft lip with or without cleft palate (CL(P)) and isolated cleft palate (CP) are separ...
none11BACKGROUND: Genetic studies have demonstrated that non-syndromic cleft is composed of two sepa...
Background : Isolated, nonsyndromic cleft lip with or without cleft palate is a common human congeni...
Background: Cleft lip and palate are congenital disorders which induce affected individuals med...
Objective: To assess the possible association between TGFB3 allele variants and nonsyndromic cleft l...
OBJECTIVE: Orofacial clefts (OFCs) are one of the most common birth defects in humans. They are the...
Objectives: Orofacial clefts are major human birth defects with complex etiology. Previous studies h...
Context: Non Syndromic Cleft lip/Palate is a congenital anomaly with significant medical, psychologi...
We performed ameta-analysis of the association of transforming growth factor α gene (TGFA) polymorph...
OBJECTIVES: Nonsyndromic cleft lip with or without cleft palate (CL/P) is a frequent craniofacial ma...
 Objective: This study aimed to detect and analyze transforming growth factor alpha (TGFA) BamHI an...
Background: Genetic studies have demonstrated that non-syndromic cleft is composed of two separate e...
Cleft lip with or without cleft palate and cleft palate alone are the most common craniofacial anom...
Genetic studies have demonstrated that nonsyndromic cleft is composed of two separate entities: the ...
Introduction: Non-syndromic cleft lip with or without cleft palate (NCL±P) is characterized by a mul...
Background - Cleft lip with or without cleft palate (CL(P)) and isolated cleft palate (CP) are separ...
none11BACKGROUND: Genetic studies have demonstrated that non-syndromic cleft is composed of two sepa...
Background : Isolated, nonsyndromic cleft lip with or without cleft palate is a common human congeni...
Background: Cleft lip and palate are congenital disorders which induce affected individuals med...
Objective: To assess the possible association between TGFB3 allele variants and nonsyndromic cleft l...
OBJECTIVE: Orofacial clefts (OFCs) are one of the most common birth defects in humans. They are the...