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American journal of human genetics
American journal of human genetics
Medical sequencing at the extremes of human body mass.
Deletions in CCM2 are a common cause of cerebral cavernous malformations.
Deletions in CCM2 are a common cause of cerebral cavernous malformations.
A high-density screen for linkage in multiple sclerosis.
A high-density screen for linkage in multiple sclerosis.
The R620W polymorphism of the protein tyrosine phosphatase PTPN22 is not associated with multiple sclerosis.
The R620W polymorphism of the protein tyrosine phosphatase PTPN22 is not associated with multiple sclerosis.
Mapping a Mendelian form of intracranial aneurysm to 1p34.3-p36.13.
Mapping a Mendelian form of intracranial aneurysm to 1p34.3-p36.13.
A second-generation genomic screen for multiple sclerosis.
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