N. Morgan

发表

Association of complementation group and mutation type with clinical outcome in fanconi anemia. European Fanconi Anemia Research Group.

C. Lewis, C. Mathew, T. de Ravel, 2000, Blood.

A patient-derived mutant form of the Fanconi anemia protein, FANCA, is defective in nuclear accumulation.

C. Mathew, A. D’Andrea, I. Garcı́a-Higuera, 1999, Experimental hematology.

Positive diepoxybutane test in only one of two brothers found to be compound heterozygotes for Fanconi's anaemia complementation group C mutations

I. Roberts, I. Dokal, G. Hall, 1996, British journal of haematology.

Heterogeneous spectrum of mutations in the Fanconi anaemia group A gene

G. Pals, R. Gibson, J. Cavenagh, 1999, European Journal of Human Genetics.

Isolation of a cDNA representing the Fanconi anemia complementation group E gene.

N. Alon, C. Mathew, Q. Waisfisz, 2000, American journal of human genetics.

High frequency of large intragenic deletions in the Fanconi anemia group A gene.

C. Mathew, H. Joenje, N. Morgan, 1999, American journal of human genetics.

VACTERL with hydrocephalus in twins due to Fanconi anemia (FA): mutation in the FAC gene.

R. Gibson, L. Brueton, N. Morgan, 1997, American journal of medical genetics.

Deletion and reduced expression of the Fanconi anemia FANCA gene in sporadic acute myeloid leukemia

I. Vořechovský, S. Hodgson, S. Hodgson, 2004, Leukemia.

Complementation analysis in Fanconi anemia: assignment of the reference FA-H patient to group A.

C. Mathew, Q. Waisfisz, A. D’Andrea, 2000, American journal of human genetics.

The Fanconi anemia group E gene, FANCE, maps to chromosome 6p.

C. Mathew, Q. Waisfisz, R. Wegner, 1999, American journal of human genetics.