The search for HLA association in spina bifida is particularly interesting since this condition can be associated with the effects of the T locus in mice. Gene and haplotype frequencies in 32 unrelated patients suffering from spina bifida were studied. Gene frequency of HLA-B5 and haplotype frequency of A2, B5 were increased without reaching signification levels. Fourteen families were examined clinically and radiologically. A high frequency of spina bifida occulta and other vertebral abnormalities was found without evidence of linkage with HLA haplotypes
The HLA system was first defined as a cell surface genetic polymorphism with the aim of using it for...
The spinocerebellar ataxias (SCAs) are a heterogeneous group of neurodegenerative disorders characte...
Spina bifida and genetic factors related to myo-inositol, glucose, and zinc. Groenen PM, Klootwijk R...
The spina bifida/anencephaly complex in man in some ways resembles the effects of T-locus mutants in...
The authors report a genetic study of a family with spino-cerebellar ataxia and indicate that an ass...
The authors test single nucleotide polymorphisms (SNPs) in coding sequences of 12 candidate genes in...
Five families with late onset autosomal dominant spinocerebellar ataxia, were studied. Linkage betwe...
Five families with late onset autosomal dominant spinocerebellar ataxia, were studied. Linkage betwe...
Neural tube defects (NTDs) are the most common severely disabling birth defects in the United States...
Spina bifida is among the phenotypes of the larger condition known as neural tube defects (NTDs). It...
The autosomal dominant spinocerebellar ataxias (SCAs) are a clinically heterogeneous group of neurod...
BackgroundSpina bifida is a malformation of the neural tube and is the most common of neural tube de...
We studied three large kindreds with the HLA-linked form of spinocerebellar ataxia (SCA1) in order ...
Spina bifida (SB) is a debilitating birth defect caused by multiple gene and environment interaction...
peer reviewedThe aetiology of spina bifida involves genetic and environmental factors, which may be ...
The HLA system was first defined as a cell surface genetic polymorphism with the aim of using it for...
The spinocerebellar ataxias (SCAs) are a heterogeneous group of neurodegenerative disorders characte...
Spina bifida and genetic factors related to myo-inositol, glucose, and zinc. Groenen PM, Klootwijk R...
The spina bifida/anencephaly complex in man in some ways resembles the effects of T-locus mutants in...
The authors report a genetic study of a family with spino-cerebellar ataxia and indicate that an ass...
The authors test single nucleotide polymorphisms (SNPs) in coding sequences of 12 candidate genes in...
Five families with late onset autosomal dominant spinocerebellar ataxia, were studied. Linkage betwe...
Five families with late onset autosomal dominant spinocerebellar ataxia, were studied. Linkage betwe...
Neural tube defects (NTDs) are the most common severely disabling birth defects in the United States...
Spina bifida is among the phenotypes of the larger condition known as neural tube defects (NTDs). It...
The autosomal dominant spinocerebellar ataxias (SCAs) are a clinically heterogeneous group of neurod...
BackgroundSpina bifida is a malformation of the neural tube and is the most common of neural tube de...
We studied three large kindreds with the HLA-linked form of spinocerebellar ataxia (SCA1) in order ...
Spina bifida (SB) is a debilitating birth defect caused by multiple gene and environment interaction...
peer reviewedThe aetiology of spina bifida involves genetic and environmental factors, which may be ...
The HLA system was first defined as a cell surface genetic polymorphism with the aim of using it for...
The spinocerebellar ataxias (SCAs) are a heterogeneous group of neurodegenerative disorders characte...
Spina bifida and genetic factors related to myo-inositol, glucose, and zinc. Groenen PM, Klootwijk R...