Pages that link to "Q34103884"
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The following pages link to The association analysis of TBX6 polymorphism with susceptibility to congenital scoliosis in a Chinese Han population. (Q34103884):
Displaying 16 items.
- TBX6, LHX1 and copy number variations in the complex genetics of Müllerian aplasia (Q21202853) (← links)
- TBX6 null variants and a common hypomorphic allele in congenital scoliosis (Q35078357) (← links)
- Sequencing of the TBX6 Gene in Families with Familial Idiopathic Scoliosis (Q35781950) (← links)
- A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disorders (Q36386207) (← links)
- Analysis of single nucleotide polymorphism in adolescent idiopathic scoliosis in Korea: for personalized treatment (Q36620379) (← links)
- Animal models for scoliosis research: state of the art, current concepts and future perspective applications (Q36740111) (← links)
- Clinical, genetic and environmental factors associated with congenital vertebral malformations (Q36802361) (← links)
- Genetic aspects of congenital and idiopathic scoliosis (Q37288471) (← links)
- Five known tagging DLL3 SNPs are not associated with congenital scoliosis: A case-control association study in a Chinese Han population (Q37605667) (← links)
- Progress and perspective of TBX6 gene in congenital vertebral malformations (Q37636813) (← links)
- Vertebrate segmentation: from cyclic gene networks to scoliosis (Q37881028) (← links)
- Chromosomal contacts connect loci associated with autism, BMI and head circumference phenotypes (Q41001236) (← links)
- Intra-family phenotypic heterogeneity of 16p11.2 deletion carriers in a three-generation Chinese family (Q50312865) (← links)
- Clinical and genetic aspects of Mayer-Rokitansky-Küster-Hauser syndrome. (Q52661767) (← links)
- The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease (Q58067577) (← links)
- Submicroscopic aberrations of chromosome 16 in prenatal diagnosis (Q92485593) (← links)