A TaqI RFLP in Xq26----qter detected by pX301b [DXS311]

por Sood, R, White, B N, Holden, J J
Publicado 1989

Molecular analysis of X-autosome translocations in females with Duchenne muscular dystrophy.

por Bodrug, S E, Holden, J J, Ray, P N, Worton, R G
Publicado 1991

Isolation and mapping of a polymorphic DNA sequence, DXS312, to Xq27----Xq28.

por Mulligan, L, Sood, R, Poon, R, White, B N, Holden, J J
Publicado 1989

Genetic mapping of two new DNA markers in Xq26-q28 relative to the fragile-X syndrome locus.

por Sood, R, Mulligan, L M, Poon, R, White, B N, Holden, J J
Publicado 1990

A gene family in Drosophila melanogaster coding for trypsin-like enzymes.

por Davis, C A, Riddell, D C, Higgins, M J, Holden, J J, White, B N
Publicado 1985

Genetic Characterization of the Region between 86f1,2 and 87b15 on Chromosome 3 of DROSOPHILA MELANOGASTER

por Gausz, J., Gyurkovics, H., Bencze, G., Awad, A. A. M., Holden, J. J., Ish-Horowicz, D.
Publicado 1981

The fragile X premutation in carriers and its effect on mutation size in offspring.

por Fisch, G S, Snow, K, Thibodeau, S N, Chalifaux, M, Holden, J J, Nelson, D L, Howard-Peebles, P N, Maddalena, A
Publicado 1995

FMR1 in global populations.

por Kunst, C. B., Zerylnick, C., Karickhoff, L., Eichler, E., Bullard, J., Chalifoux, M., Holden, J. J., Torroni, A., Nelson, D. L., Warren, S. T.
Publicado 1996

Genetic mapping of DNA segments relative to the locus for the fragile-X syndrome at Xq27.3.

por Mulligan, L M, Phillips, M A, Forster-Gibson, C J, Beckett, J, Partington, M W, Simpson, N E, Holden, J J, White, B N
Publicado 1985

A polymorphic locus, D10S5, at 10q21.1.

por McDermid, H E, Goodfellow, P J, Duncan, A M, Brasch, K R, Simpson, N E, Souza, C D, Holden, J J, White, B N
Publicado 1987

Linkage analysis of a DNA marker localized to 20p12 and multiple endocrine neoplasia type 2A.

por Goodfellow, P J, White, B N, Holden, J J, Duncan, A M, Sears, E V, Wang, H S, Berlin, L, Kidd, K K, Simpson, N E
Publicado 1985

An efficient strategy for gene mapping using multipoint linkage analysis: exclusion of the multiple endocrine neoplasia 2A (MEN2A) locus from chromosome 13.

por Farrer, L A, Goodfellow, P J, Lamarche, C M, Franjkovic, I, Myers, S, White, B N, Holden, J J, Kidd, J R, Simpson, N E, Kidd, K K
Publicado 1987

Clinical and molecular cytogenetic characterisation of a newly recognised microdeletion syndrome involving 2p15‐16.1

por Rajcan‐Separovic, E, Harvard, C, Liu, X, McGillivray, B, Hall, J G, Qiao, Y, Hurlburt, J, Hildebrand, J, Mickelson, E C R, Holden, J J A, Lewis, M E S
Publicado 2007

Threat to Hospital Privileges

por Attenborough, John, Aubrey, D. Roland, Auger, H., Austin, A. J., Bartlett, Calum I. S., Bellamy, R. C. T., Bergel, Richard C., Bryant, David, Carpenter, Michael E., Cates, Richard, Christmas, A. R., Clyne, G. Elsa, Collings-Wells, John A., Crawshaw, P. F. A., Cule, John H., Dobbin, L. W. B., Donovan, Brian, Edwards, John, Evans, Keith M., Faber, Vernon C., France, Richard, Gent, N. S. C., Hadfield, George W., Haskins, T. D., Henley, Brian, Henry, D. O., Holden, J. J., James, John P., Kayll, J. N., Kent, S. G., Key, Ian A., Kieft, B. T., Wright, M. F. Lind, Lister, C. O., MacAdam, A. D., McNutt, Joe, Mason, J. Y. J. M., Mason, D. Paul, Mathewson, Jack, May, William, Morrison, Robert W. M., Narula, Y. P., Price, J. C. Newell, Norman, J. M., Page, H. J. Clifford, Perry, J. R., Poole, P. B., Porter, Alan M. W., Powell, John K., Poyntz-Wright, R. C., Price, D. J., Price, John, Pritchard, J. N. A., Robinson, Ian H., Rust, Nigel E., Scriven, Jeanne M., Singer, Geoffrey E., Smart, Peter C., Smith, Paul S., Summerhayes, John L. V., Tilly, Clifford R., Tipler, H. Bolton, Trust, Desmond G. L., Turner, A. G., Urquhart, D. R. H., Walker, Colin D., Wallace, Ian W., Watson, M., Whitehouse, Michael S., Whittingham, M. Anne, Whittingham, W., Williams, Eileen M., Winchurch, Brian
Publicado 1968