P. Jacobs

A reinvestigation of non-disjunction resulting in 47, XXY males of paternal origin

N. S. Thomas, P. Jacobs, T. Hassold, 2000, European Journal of Human Genetics.

A study of females with deletions of the short arm of the X chromosome

D. Skuse, A. Sharp, N. S. Thomas, 1998, Human Genetics.

De novo deletions and duplications detected by array CGH: a study of parental origin in relation to mechanisms of formation and size of imbalance

J. Crolla, N. S. Thomas, P. Jacobs, 2011, European Journal of Human Genetics.

Parental and chromosomal origins of microdeletion and duplication syndromes involving 7q11.23, 15q11-q13 and 22q11

R. Sandford, N. S. Thomas, P. Jacobs, 2006, European Journal of Human Genetics.

Breakpoint mapping and array CGH in translocations: comparison of a phenotypically normal and an abnormal cohort.

N. Carter, V. Maloney, J. Crolla, 2008, American journal of human genetics.

Cytogenetic and molecular studies of trisomy 13.

M. Leppert, P. Jacobs, T. Hassold, 1987, Journal of medical genetics.

Maternal folate polymorphisms and the etiology of human nondisjunction.

S. Schwartz, N. S. Thomas, P. Jacobs, 2001, American journal of human genetics.