Publications

Showing 4 of 4 Publications

1997

Homozygosity by descent for a rare mutation in the myophosphorylase gene is associated with variable phenotypes in a Druze family with McArdle disease.
Iyengar S, Kalinsky H, Weiss S, Korostishevsky M, Sadeh M, Zhao Y, Kidd K, Bonne-Tamir B. Homozygosity by descent for a rare mutation in the myophosphorylase gene is associated with variable phenotypes in a Druze family with McArdle disease. Journal Of Medical Genetics 1997, 34: 391. PMID: 9152836, PMCID: PMC1050946, DOI: 10.1136/jmg.34.5.391.
Peer-Reviewed Original Research
MeSH Keywords

1995

Evidence for inter-generational instability in the CAG repeat in the MJD1 gene and for conserved haplotypes at flanking markers amongst Japanese and Caucasian subjects with Machado-Joseph disease
Takiyama Y, Igasrashi S, Rogaeva E, Endo K, Rogaev E, Tanaka H, Sherrington R, Sanpei K, Liang Y, Saito M, Tsuda T, Takano H, Ikeda M, Lin C, Chi H, Kennedy J, Lang A, Wherrett J, Segawa M, Nomura Y, Yuasa T, Weissenbach J, Yoshida M, Nishizawa M, Kidd K, Tsuji S, St George-Hyslop P. Evidence for inter-generational instability in the CAG repeat in the MJD1 gene and for conserved haplotypes at flanking markers amongst Japanese and Caucasian subjects with Machado-Joseph disease. Human Molecular Genetics 1995, 4: 1137-1146. PMID: 8528200, DOI: 10.1093/hmg/4.7.1137.
Peer-Reviewed Original Research
MeSH Keywords

1980

Genetics of propionic acidemia in a Mennonite-Amish kindred.
Kidd J, Wolf B, Hsia E, Kidd K. Genetics of propionic acidemia in a Mennonite-Amish kindred. American Journal Of Human Genetics 1980, 32: 236-45. PMID: 7386459, PMCID: PMC1686010.
Peer-Reviewed Original Research
MeSH Keywords

1976

Estimating the genetic contribution to schizophrenia
Matthysse S, Kidd K. Estimating the genetic contribution to schizophrenia. American Journal Of Psychiatry 1976, 133: 185-191. PMID: 1251925, DOI: 10.1176/ajp.133.2.185.
Peer-Reviewed Original Research
MeSH Keywords

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