The Child with Multiple Birth Defects

por McKeown, C
Publicado 1988

An autosomal dominant multiple pterygium syndrome.

por McKeown, C M, Harris, R
Publicado 1988

Mutagen-induced resistance to mycophenolic acid in hamster cells can be associated with increased inosine 5'-phosphate dehydrogenase activity.

por Huberman, E, McKeown, C K, Friedman, J
Publicado 1981

Hypomelanosis of Ito: a manifestation of mosaicism or chimerism.

por Donnai, D, Read, A P, McKeown, C, Andrews, T
Publicado 1988

Molecular analysis of the APC gene in 205 families: extended genotype-phenotype correlations in FAP and evidence for the role of APC amino acid changes in colorectal cancer predisp...

por Wallis, Y., Morton, D., McKeown, C., Macdonald, F.
Publicado 1999

Reversible developmental stasis in response to nutrient availability in the Xenopus laevis central nervous system

por McKeown, C. R., Thompson, C. K., Cline, H. T.
Publicado en J Exp Biol (2017)

Parents' responses to predictive genetic testing in their children: report of a single case study.

por Michie, S, McDonald, V, Bobrow, M, McKeown, C, Marteau, T
Publicado 1996

Reviewing earlier diagnoses of chromosome.

por Chung, L C, Debelle, G, Roberts, E, McKeown, C
Publicado 1995

Tamoxifen retinopathy.

por McKeown, C A, Swartz, M, Blom, J, Maggiano, J M
Publicado 1981

Examination of fetuses after induced abortion for fetal abnormality.

por Clayton-Smith, J, Farndon, P A, McKeown, C, Donnai, D
Publicado 1990

Detection of an atypical 22q11 deletion that has no overlap with the DiGeorge syndrome critical region.

por O'Donnell, H, McKeown, C, Gould, C, Morrow, B, Scambler, P
Publicado 1997

An interaction between the mammalian DNA repair protein XRCC1 and DNA ligase III.

por Caldecott, K W, McKeown, C K, Tucker, J D, Ljungquist, S, Thompson, L H
Publicado 1994

Floating-Harbor syndrome.

por Patton, M A, Hurst, J, Donnai, D, McKeown, C M, Cole, T, Goodship, J
Publicado 1991

Wolf-Hirschhorn locus is distal to D4S10 on short arm of chromosome 4.

por McKeown, C, Read, A P, Dodge, A, Stecko, O, Mercer, A, Harris, R
Publicado 1987

Noonan's and DiGeorge syndromes with monosomy 22q11.

por Wilson, D I, Britton, S B, McKeown, C, Kelly, D, Cross, I E, Strobel, S, Scambler, P J
Publicado 1993

New domains of neural cell-adhesion molecule L1 implicated in X-linked hydrocephalus and MASA syndrome.

por Jouet, M, Moncla, A, Paterson, J, McKeown, C, Fryer, A, Carpenter, N, Holmberg, E, Wadelius, C, Kenwrick, S
Publicado 1995

Linkage relationships between X-linked retinitis pigmentosa and nine short-arm markers: exclusion of the disease locus from Xp21 and localization to between DXS7 and DXS14.

por Wright, A F, Bhattacharya, S S, Clayton, J F, Dempster, M, Tippett, P, McKeown, C M, Jay, M, Jay, B, Bird, A C
Publicado 1987

Mapping of the X linked form of hyper IgM syndrome (HIGM1)

por Padayachee, M, Levinsky, R J, Kinnon, C, Finn, A, McKeown, C, Feighery, C, Notarangelo, L D, Hendriks, R W, Read, A P, Malcolm, S
Publicado 1993

Germline mutations of the LKB1 (STK11) gene in Peutz-Jeghers patients

por Wang, Z, Churchman, M, Avizienyte, E, McKeown, C, Davies, S, Evans, D, Ferguson, A, Ellis, I, Xu, W., Yan, Z., Aaltonen, L, Tomlinson, I
Publicado 1999

A protease-based biosensor for the detection of schistosome cercariae

por Webb, A. J., Kelwick, R., Doenhoff, M. J., Kylilis, N., MacDonald, J. T., Wen, K. Y., McKeown, C., Baldwin, G., Ellis, T., Jensen, K., Freemont, P. S.
Publicado en Sci Rep (2016)