Autosomal dominant hypophosphatemic rickets is linked to chromosome 12p13.

Por Econs, M J, McEnery, P T, Lennon, F, Speer, M C
Publicado em 1997

Using neural networks as an aid in the determination of disease status: comparison of clinical diagnosis to neural-network predictions in a pedigree with autosomal dominant limb-gi...

Por Falk, C T, Gilchrist, J M, Pericak-Vance, M A, Speer, M C
Publicado em 1998

Linkage of familial dilated cardiomyopathy with conduction defect and muscular dystrophy to chromosome 6q23.

Por Messina, D N, Speer, M C, Pericak-Vance, M A, McNally, E M
Publicado em 1997

Power calculations for likelihood ratio tests for offspring genotype risks, maternal effects and parent-of-origin (POO) effects in the presence of missing parental genotypes when u...

Por Rampersaud, E., Morris, R.W., Weinberg, C.R., Speer, M.C., Martin, E.R.
Publicado em 2007

A PstI polymorphism detected by a genomic clone at the human slow troponin T (TNNT1) gene locus

Por Samson, F., Gilbert, J.R., Koza-Taylor, P., Speer, M.C., Lee, J., Roses, A.D.
Publicado em 1991

Evidence for linkage disequilibrium in chromosome 13-linked Duchenne-like muscular dystrophy (LGMD2C)

Por Ben Othmane, K, Speer, M C, Stauffer, J, Blel, S, Middleton, L, Ben Hamida, C, Etribi, A, Loeb, D, Hentati, F, Roses, A D
Publicado em 1995

Misclassification and linkage of hereditary sensory and autonomic neuropathy type 1 as Charcot-Marie-Tooth disease, type 2B.

Por Vance, J. M., Speer, M. C., Stajich, J. M., West, S., Wolpert, C., Gaskell, P., Lennon, F., Tim, R. M., Rozear, M., Othmane, K. B.
Publicado em 1996

Familial inheritance of a DXS164 deletion mutation from a heterozygous female.

Por Lanman, J T, Pericak-Vance, M A, Bartlett, R J, Chen, J C, Yamaoka, L, Koh, J, Speer, M C, Hung, W Y, Roses, A D
Publicado em 1987

Transcriptome Profiling of Genes Involved in Neural Tube Closure During Human Embryonic Development Using Long Serial Analysis of Gene Expression (Long-SAGE)

Por Krupp, D. R., Xu, P-T., Thomas, S., Dellinger, A., Etchevers, H. C., Vekemans, M., Gilbert, J. R., Speer, M.C., Ashley-Koch, A. E., Gregory, S. G.
Publicado em 2012

MspI RFLP for microtubule associated protein-2 (MAP2)

Por Alberts, M.J., Kandt, R.S., Pericak-Vance, M.A., Bebout, J., Speer, M.C., Siddique, T.S., Yamaoka, L., Hung, W.-Y., Gaskell, P.C., Roses, A.D.
Publicado em 1991

A StuI polymorphism on chromosome 3p14.1-14.2 (D3S622) defined by two polymorphic StuI sites 2.4 kb apart.

Por Secore, S L, Walker, A P, Herbstreith, M H, Siddique, T, Jeffers, A J, DeShields, T R, Speer, M C, Pericak-Vance, M A, Golembieski, W A, Smith, D I
Publicado em 1991

Evidence for anticipation in autosomal dominant limb-girdle muscular dystrophy.

Por Speer, M C, Gilchrist, J M, Stajich, J M, Gaskell, P C, Westbrook, C A, Horrigan, S K, Bartoloni, L, Yamaoka, L H, Scott, W K, Pericak-Vance, M A
Publicado em 1998

Linkage studies in facioscapulohumeral muscular dystrophy (FSHD)

Por Gilbert, J. R., Stajich, J. M., Speer, M. C., Vance, J. M., Stewart, C. S., Yamaoka, L. H., Samson, F., Fardeau, M., Potter, T. G., Roses, A. D., Pericak-Vance, M. A.
Publicado em 1992

Exclusion mapping of chromosomal regions which cross hybridise to FSHD1A associated markers in FSHD1B

Por Gilbert, J R, Speer, M C, Stajich, J, Clancy, R, Lewis, K, Qiu, H, Yamaoka, L, Kumar, A, Vance, J, Stewart, C, Rozear, M, Roses, A D, Pericak-Vance, M A
Publicado em 1995

Identification of a new autosomal dominant limb-girdle muscular dystrophy locus on chromosome 7.

Por Speer, M C, Vance, J M, Grubber, J M, Lennon Graham, F, Stajich, J M, Viles, K D, Rogala, A, McMichael, R, Chutkow, J, Goldsmith, C, Tim, R W, Pericak-Vance, M A
Publicado em 1999

Evidence for heterogeneity in facioscapulohumeral muscular dystrophy (FSHD)

Por Gilbert, J. R., Stajich, J. M., Wall, S., Carter, S. C., Qiu, H., Vance, J. M., Stewart, C. S., Speer, M. C., Pufky, J., Yamaoka, L. H., Rozear, M., Samson, F., Fardeau, M., Roses, A. D., Pericak-Vance, M. A.
Publicado em 1993

A functional alternative splicing mutation in human tryptophan hydroxylase-2

Por Zhang, X, Nicholls, P J, Laje, G, Sotnikova, T D, Gainetdinov, R R, Albert, P R, Rajkowska, G, Stockmeier, C A, Speer, M C, Steffens, D C, Austin, M C, McMahon, F J, Krishnan, K R R, Garcia-Blanco, M A, Caron, M G
Publicado em 2011

Assignment of a gene (NEM1) for autosomal dominant nemaline myopathy to chromosome 1

Por Laing, N. G., Majda, B. T., Akkari, P. A., Layton, M. G., Mulley, J. C., Phillips, H., Haan, E. A., White, S. J., Beggs, A. H., Kunkel, L. M., Groth, D. M., Boundy, K. L., Kneebone, C. S., Blumberg, P. C., Wilton, S. D., Speer, M. C., Kakulas, B. A.
Publicado em 1992