C. Papapetrou

Mutations of UFD1L are not responsible for the majority of cases of DiGeorge Syndrome/velocardiofacial syndrome without deletions within chromosome 22q11.

J. Osinga, R. Hofstra, B. Dallapiccola, 1999, American journal of human genetics.

Mutation analysis and embryonic expression of the HLXB9 Currarino syndrome gene.

P. Scambler, W. Reardon, R. Winter, 2000, American journal of human genetics.

The T transcription factor functions as a dimer and exhibits a common human polymorphism Gly‐177‐Asp in the conserved DNA‐binding domain

J. Sowden, Y. Edwards, C. Papapetrou, 1997, FEBS letters.

Susceptibility to spina bifida; an association study of five candidate genes

J. Burn, F. Hol, K. Morrison, 1998, Annals of human genetics.

Genetic mapping of the human homologue (T) of mouse T(Brachyury) and a search for allele association between human T and spina bifida.

E. Mariman, J. Attwood, J. Burn, 1996, Human molecular genetics.

Methylenetetrahydrofolate reductase and neural tube defects

J. Burn, Y. Edwards, S. Lynch, 1996, The Lancet.

The human TBX6 gene: cloning and assignment to chromosome 16p11.2.

M. Fox, Y. Edwards, W. Putt, 1999, Genomics.