| scholarly article | Q13442814 |
| P50 | author | Alexander F Wilson | Q64481879 |
| P2093 | author name string | Nancy H Miller | |
| Mera K Tilley | |||
| Beth Marosy | |||
| Cristina M Justice | |||
| Kandice Swindle | |||
| P2860 | cites work | Scoliosis in twins. A meta-analysis of the literature and report of six cases | Q73719623 |
| The incidence of scoliosis in the state of Delaware; a study of 50,000 minifilms of the chest made during a survey for tuberculosis | Q73851912 | ||
| Characterization of idiopathic scoliosis in a clinically well-defined population | Q77207007 | ||
| Association between estrogen receptor gene polymorphisms and curve severity of idiopathic scoliosis | Q78534592 | ||
| SNP rs11190870 near LBX1 is associated with adolescent idiopathic scoliosis in southern Chinese | Q83388357 | ||
| HEREDITARY SCOLIOSIS | Q84930536 | ||
| Haploview: analysis and visualization of LD and haplotype maps | Q27860955 | ||
| Mutation update on the CHD7 gene involved in CHARGE syndrome | Q28263190 | ||
| Genetics of adolescent idiopathic scoliosis | Q33588386 | ||
| Segregation analysis of idiopathic scoliosis: demonstration of a major gene effect | Q33874747 | ||
| Promoter polymorphism of matrilin-1 gene predisposes to adolescent idiopathic scoliosis in a Chinese population | Q34326007 | ||
| Curve characteristics in monozygotic twins with adolescent idiopathic scoliosis: 3 new twin pairs and a review of the literature | Q34510935 | ||
| Melatonin receptor 1B (MTNR1B) gene polymorphism is associated with the occurrence of adolescent idiopathic scoliosis. | Q34651172 | ||
| Autosomal dominant Marfan-like connective-tissue disorder with aortic dilation and skeletal anomalies not linked to the fibrillin genes | Q35194631 | ||
| CHD7 gene polymorphisms are associated with susceptibility to idiopathic scoliosis. | Q35752651 | ||
| Osteoporosis and familial idiopathic scoliosis: association with an abnormal alpha 2(I) collagen | Q44333622 | ||
| Adolescent idiopathic scoliosis in identical twins. | Q44454751 | ||
| Association of estrogen receptor beta gene polymorphisms with susceptibility to adolescent idiopathic scoliosis | Q46178652 | ||
| A novel classification system to predict the pathogenic effects of CHD7 missense variants in CHARGE syndrome. | Q47844332 | ||
| Familial idiopathic scoliosis: evidence of an X-linked susceptibility locus | Q48028860 | ||
| Genetic aspects of idiopathic scoliosis. A Nicholas Andry Award essay, 1970. | Q48424195 | ||
| A genome-wide association study identifies common variants near LBX1 associated with adolescent idiopathic scoliosis. | Q50998791 | ||
| Implementing a unified approach to family-based tests of association. | Q52072093 | ||
| Association study of BMP4, IL6, Leptin, MMP3, and MTNR1B gene promoter polymorphisms and adolescent idiopathic scoliosis. | Q54392918 | ||
| Adolescent Idiopathic Scoliosis in Twins | Q61567102 | ||
| Scoliosis prevalence: a call for a statement of terms | Q67052232 | ||
| A genetic survey of idiopathic scoliosis in Boston, Massachusetts | Q69621307 | ||
| Nonstandard vertebral rotation in scoliosis screening patients. Its prevalence and relation to the clinical deformity | Q70323254 | ||
| Familial (idiopathic) scoliosis. A family survey | Q72029247 | ||
| P433 | issue | 22 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | scoliosis | Q174857 |
| P304 | page(s) | E1432-6 | |
| P577 | publication date | 2013-10-01 | |
| P1433 | published in | Spine | Q7577526 |
| P1476 | title | CHD7 gene polymorphisms and familial idiopathic scoliosis | |
| P478 | volume | 38 |
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