Maximum-likelihood analysis of human T-cell X chromosome inactivation patterns: normal women versus carriers of X-linked severe combined immunodeficiency. Read more about Maximum-likelihood analysis of human T-cell X chromosome inactivation patterns: normal women versus carriers of X-linked severe combined immunodeficiency.
Strong allelic association between the torsion dystonia gene (DYT1) andloci on chromosome 9q34 in Ashkenazi Jews. Read more about Strong allelic association between the torsion dystonia gene (DYT1) andloci on chromosome 9q34 in Ashkenazi Jews.
Homozygosity for a newly identified missense mutation in a patient with very severe combined immunodeficiency due to adenosine deaminase deficiency (ADA-SCID). Read more about Homozygosity for a newly identified missense mutation in a patient with very severe combined immunodeficiency due to adenosine deaminase deficiency (ADA-SCID).
Estimation of morbid risk and age at onset with missing information. Read more about Estimation of morbid risk and age at onset with missing information.
A note on multiple testing procedures in linkage analysis. Read more about A note on multiple testing procedures in linkage analysis.
Estimation of allele frequencies for VNTR loci. Read more about Estimation of allele frequencies for VNTR loci.
Genetic analysis of breast cancer in the cancer and steroid hormone study. Read more about Genetic analysis of breast cancer in the cancer and steroid hormone study.
Human carboxypeptidase A identifies a BglII RFLP and maps to 7q31-qter. Read more about Human carboxypeptidase A identifies a BglII RFLP and maps to 7q31-qter.
Segregation analysis of idiopathic torsion dystonia in Ashkenazi Jews suggests autosomal dominant inheritance. Read more about Segregation analysis of idiopathic torsion dystonia in Ashkenazi Jews suggests autosomal dominant inheritance.
Linkage strategies for genetically complex traits. III. The effect of marker polymorphism on analysis of affected relative pairs. Read more about Linkage strategies for genetically complex traits. III. The effect of marker polymorphism on analysis of affected relative pairs.
