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L Yamaoka

Showing results (1-10 of 15) with videos related to

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Nucleic Acids Research|July 11, 1986
RFLPs at the D19S19 locus of human chromosome 19 linked to myotonic dystrophy (DM)A D Roses, M A Pericak-Vance, D A Ross, et al.
Neurology|April 1, 1990
Presymptomatic and prenatal diagnosis in myotonic dystrophy by genetic linkage studiesM C Speer, M A Pericak-Vance, L Yamaoka, et al.
Australian Paediatric Journal|January 1, 1988
Update on the molecular genetics of Duchenne muscular dystrophyT Siddique, R Bartlett, M Pericak-Vance, et al.
Journal of Medical Genetics|October 1, 1995
Exclusion mapping of chromosomal regions which cross hybridise to FSHD1A associated markers in FSHD1BJ R Gilbert, M C Speer, J Stajich, et al.
Nucleic Acids Research|July 25, 1991
RsaI RFLP for electron transport flavoprotein-beta(ETFB)V Royal, M J Alberts, M A Pericak-Vance, et al.
Science (New York, N.Y.)|March 27, 1987
A new probe for the diagnosis of myotonic muscular dystrophyR J Bartlett, M A Pericak-Vance, L Yamaoka, et al.
Progress in Clinical and Biological Research|January 1, 1989
Linkage studies in familial Alzheimer's diseaseA D Roses, M A Pericak-Vance, L Yamaoka, et al.
Australian Paediatric Journal|January 1, 1988
Systematic gene mapping in man: data management considerationsM A Pericak-Vance, W Y Hung, L Yamaoka, et al.
American Journal of Human Genetics|August 1, 1987
Familial inheritance of a DXS164 deletion mutation from a heterozygous femaleJ T Lanman, M A Pericak-Vance, R J Bartlett, et al.
Annals of Neurology|November 1, 1996
Confirmation of linkage of oculopharyngeal muscular dystrophy to chromosome 14q11.2-q13J M Stajich, J M Gilchrist, F Lennon, et al.
Pageof 2

Showing results (1-10 of 15) with videos related to

Sort By:
Pageof 2
Nucleic Acids Research|July 11, 1986
RFLPs at the D19S19 locus of human chromosome 19 linked to myotonic dystrophy (DM)A D Roses, M A Pericak-Vance, D A Ross, et al.
Neurology|April 1, 1990
Presymptomatic and prenatal diagnosis in myotonic dystrophy by genetic linkage studiesM C Speer, M A Pericak-Vance, L Yamaoka, et al.
Australian Paediatric Journal|January 1, 1988
Update on the molecular genetics of Duchenne muscular dystrophyT Siddique, R Bartlett, M Pericak-Vance, et al.
Journal of Medical Genetics|October 1, 1995
Exclusion mapping of chromosomal regions which cross hybridise to FSHD1A associated markers in FSHD1BJ R Gilbert, M C Speer, J Stajich, et al.
Nucleic Acids Research|July 25, 1991
RsaI RFLP for electron transport flavoprotein-beta(ETFB)V Royal, M J Alberts, M A Pericak-Vance, et al.
Science (New York, N.Y.)|March 27, 1987
A new probe for the diagnosis of myotonic muscular dystrophyR J Bartlett, M A Pericak-Vance, L Yamaoka, et al.
Progress in Clinical and Biological Research|January 1, 1989
Linkage studies in familial Alzheimer's diseaseA D Roses, M A Pericak-Vance, L Yamaoka, et al.
Australian Paediatric Journal|January 1, 1988
Systematic gene mapping in man: data management considerationsM A Pericak-Vance, W Y Hung, L Yamaoka, et al.
American Journal of Human Genetics|August 1, 1987
Familial inheritance of a DXS164 deletion mutation from a heterozygous femaleJ T Lanman, M A Pericak-Vance, R J Bartlett, et al.
Annals of Neurology|November 1, 1996
Confirmation of linkage of oculopharyngeal muscular dystrophy to chromosome 14q11.2-q13J M Stajich, J M Gilchrist, F Lennon, et al.
Pageof 2