Showing results (1-10 of 16) with videos related to
Sort By:
Pageof 2
American Journal of Human Genetics|October 1, 1992
A double mutation in exon 6 of the beta-hexosaminidase alpha subunit in a patient with the B1 variant of Tay-Sachs diseaseP J Ainsworth, M B Coulter-MackieHuman Mutation|January 1, 1997
Example of somatic mosaicism in a series of de novo neurofibromatosis type 1 cases due to a maternally derived deletionP J Ainsworth, P K Chakraborty, R WeksbergHuman Genetics|March 1, 1993
Identification and characterization of sporadic and inherited mutations in exon 31 of the neurofibromatosis (NF1) geneP J Ainsworth, D I Rodenhiser, M T CostaDevelopmental Biology|January 11, 2002
Allele-specific non-CpG methylation of the Nf1 gene during early mouse developmentT R Haines, D I Rodenhiser, P J AinsworthClinical Genetics|August 25, 2004
Family cancer histories predictive of a high risk of hereditary non-polyposis colorectal cancer associate significantly with a genomic rearrangement in hMSH2 or hMLH1P J Ainsworth, D Koscinski, B P Fraser, et al.Canadian Journal of Biochemistry|June 1, 1978
Effect of radiosensitizing agents on electron transport systemsP J Ainsworth, M Channon, R Sridhar, et al.Journal of Psychiatry & Neuroscience : JPN|March 1, 1997
A nongenetic basis of cycle frequency in bipolar disorder: study of a monozygotic twin pairV Sharma, P J Ainsworth, S B McCabe, et al.Muscle & Nerve. Supplement|January 3, 2001
Clinical and pathological observations in men lacking the gap junction protein connexin 32A F Hahn, P J Ainsworth, C C Naus, et al.Biotechnology Annual Review|January 1, 1996
Strategies and applications of DNA level diagnosis in genetic diseases: past experiences and future directionsS M Singh, D I Rodenhiser, R N Ott, et al.Acta Neuropathologica|March 29, 2001
Pathological findings in the x-linked form of Charcot-Marie-Tooth disease: a morphometric and ultrastructural analysisA F Hahn, P J Ainsworth, C F Bolton, et al.Pageof 2