S. Holloway

发表

A chromosomal deletion map of human malformations.

S Holloway, D. Fitzpatrick, A. Schinzel, 1998, American journal of human genetics.

A locus for isolated cleft palate, located on human chromosome 2q32.

A. Green, D. Bonthron, A. Markham, 1999, American journal of human genetics.

Recessive Inheritance

C. Hayward, D. Brock, W. Liston, 2006 .

A study of possible heterogeneity in Duchenne muscular dystrophy

A. Emery, S. Holloway, R. Skinner, 1979, Clinical genetics.

Survival in trisomy 13 and trisomy 18 cases ascertained from population based registers

A. Carothers, D. Fitzpatrick, C. Brewer, 2002, Journal of medical genetics.

A chromosomal duplication map of malformations: regions of suspected haplo- and triplolethality--and tolerance of segmental aneuploidy--in humans.

S Holloway, D. Fitzpatrick, A. Schinzel, 1999, American journal of human genetics.

Evidence based medicine in practice: lessons from a Scottish clinical genetics project

H. Campbell, N. Bradshaw, M. Porteous, 2000, Journal of medical genetics.

Hereditary haemorrhagic telangiectasia: a questionnaire based study to delineate the different phenotypes caused by endoglin and ALK1 mutations

A. Guttmacher, M. Porteous, D. Marchuk, 2003, Journal of medical genetics.

FISH mapping of de novo apparently balanced chromosome rearrangements identifies characteristics associated with phenotypic abnormality.

J. Clayton-Smith, J. Goodship, H. Stewart, 2008, American journal of human genetics.

A novel acropectoral syndrome maps to chromosome 7q36

J. Tolmie, F. Goodman, Y. Ozkul, 2001, Journal of medical genetics.

Linkage disequilibrium and recombination make a telomeric site for the Huntington's disease gene unlikely.

R. Snell, A. Curtis, A. Shrimpton, 1991, Journal of medical genetics.