Kathleen W. Rao

Molecular characterisation of chromosome 4p deletions resulting in Wolf-Hirschhorn syndrome.

A. Aylsworth, A. Lamb, N. Callanan, 1994, Journal of medical genetics.

An extensive de novo deletion removing FMR1 in a patient with mental retardation and the fragile X syndrome phenotype.

C. Schwartz, A. Aylsworth, A. Lachiewicz, 1993, Human molecular genetics.

Holoprosencephaly in an infant with a minute deletion of chromosome 21(q22.3).

A. Aylsworth, R. Donahue, K. Rao, 1990, American journal of medical genetics.

Functional correction of fanconi anemia group C hematopoietic cells by the use of a novel lentiviral vector.

J. Olsen, C. Walsh, K. Yamada, 2001, Molecular therapy : the journal of the American Society of Gene Therapy.

Adult de novo acute myeloid leukemia with t(6;11)(q27;q23)

C. Bloomfield, R. Larson, K. Mrózek, 2004, Cancer.

A molecular deletion of distal chromosome 4p in two families with a satellited chromosome 4 lacking the Wolf-Hirschhorn syndrome phenotype.

A. Lamb, N. Callanan, H. Kirkman, 1992, American journal of human genetics.

Neurological aspects of del(1q) syndrome.

A. Aylsworth, R. Greenwood, K. Rao, 1991, American journal of medical genetics.