Alexander F. Markham

发表

Identification of autosomal recessive disease loci using out‐bred nuclear families

Colin A. Johnson, D. Bonthron, I. Carr, 2012, Human mutation.

Mutations in the pre-mRNA splicing factor gene PRPC8 in autosomal dominant retinitis pigmentosa (RP13).

D. Mackey, F. Cremers, A. Bird, 2001, Human molecular genetics.

Loss-of-function mutations in the cathepsin C gene result in periodontal disease and palmoplantar keratosis

Emma Roberts, Philip Sloan, Michael J. Dixon, 1999, Nature Genetics.

The presence of multiple regions of homozygous deletion at the CSMD1 locus in oral squamous cell carcinoma question the role of CSMD1 in head and neck carcinogenesis

A. Read, S. Gollin, M. Dixon, 2003, Genes, chromosomes & cancer.

Primary autosomal recessive microcephaly (MCPH1) maps to chromosome 8p22-pter.

C. Woods, M. Levene, A. Markham, 1998, American journal of human genetics.

Molecular analysis of sixteen unrelated factor XIIIA deficient families from south‐east of Iran

P. Eshghi, C. Trinh, E. Miri-Moghaddam, 2008, British journal of haematology.

Factor XIII Deficiency Causing Mutation, Ser295Arg, in Exon 7 of the Factor XIIIA Gene

R. Anwar, K. Miloszewski, L. Gallivan, 2000, Thrombosis and Haemostasis.

The genetics of primary open angle glaucoma

A. Booth, A. Churchill, R. Anwar, 1997, The British journal of ophthalmology.

Genotype/phenotype correlations for coagulation factor XIII: specific normal polymorphisms are associated with high or low factor XIII specific activity.

A. Markham, R. Anwar, S. Edmonds, 1999, Blood.

New Splicing Mutations in the Human Factor XIIIA Gene, Each Producing Multiple Mutant Transcripts of Varying Abundance

A. Markham, R. Anwar, K. Miloszewski, 1998, Thrombosis and Haemostasis.

Prenatal diagnosis of aniridia.

A. Markham, I. Hanson, A. Churchill, 2000, Ophthalmology.