Parental origin of transcription from the human GNAS1 gene.

per Campbell, R, Gosden, C M, Bonthron, D T
Publicat 1994

Discordant segregation of Xq28 markers and a mutation in the L1 gene in a family with X linked hydrocephalus.

per Jouet, M, Strain, L, Bonthron, D, Kenwrick, S
Publicat 1996

Fried syndrome is a distinct X linked mental retardation syndrome mapping to Xp22.

per Strain, L, Wright, A F, Bonthron, D T
Publicat 1997

Platelet-derived growth factor A chain: gene structure, chromosomal location, and basis for alternative mRNA splicing.

per Bonthron, D T, Morton, C C, Orkin, S H, Collins, T
Publicat 1988

SmaI and HhaI polymorphisms in the 5′ region of the human von Willebrand factor gene (F8VWF)

per Strain, L., Bonthron, D.T., Brock, D.J.H.
Publicat 1991

Identification of a point mutation in the adenosine deaminase gene responsible for immunodeficiency.

per Bonthron, D T, Markham, A F, Ginsburg, D, Orkin, S H
Publicat 1985

De novo microdeletion on an inherited Robertsonian translocation chromosome: a cause for dysmorphism in the apparently balanced translocation carrier.

per Bonthron, D T, Smith, S J, Fantes, J, Gosden, C M
Publicat 1993

PMS2 mutations in childhood cancer

per Bonthron, D T, Hayward, B E, De Vos, M, Sheridan, E
Publicat 2005

Genetic heterogeneity in X-linked hydrocephalus: linkage to markers within Xq27.3.

per Strain, L., Gosden, C. M., Brock, D. J., Bonthron, D. T.
Publicat 1994

Parental consanguinity in the blepharophimosis, heart defect, hypothyroidism, mental retardation syndrome (Young-Simpson syndrome).

per Bonthron, D T, Barlow, K M, Burt, A M, Barr, D G
Publicat 1993

Platelet-derived growth factor B chain promoter contains a cis-acting fluid shear-stress-responsive element.

per Resnick, N, Collins, T, Atkinson, W, Bonthron, D T, Dewey, C F, Gimbrone, M A
Publicat 1993

Platelet-derived growth factor B chain promoter contains a cis-acting fluid shear-stress-responsive element.

per Resnick, N, Collins, T, Atkinson, W, Bonthron, D T, Dewey, C F, Gimbron, M A
Publicat 1993

Wolcott-Rallison syndrome: pathogenic insights into neonatal diabetes from new mutation and expression studies of EIF2AK3

per Brickwood, S, Bonthron, D, Al-Gazali, L, Piper, K, Hearn, T, Wilson, D, Hanley, N
Publicat 2003

Human platelet-derived growth factor A chain is transcriptionally repressed by the Wilms tumor suppressor WT1.

per Gashler, A L, Bonthron, D T, Madden, S L, Rauscher, F J, Collins, T, Sukhatme, V P
Publicat 1992

Nucleotide sequence of pre-pro-von Willebrand factor cDNA.

per Bonthron, D, Orr, E C, Mitsock, L M, Ginsburg, D, Handin, R I, Orkin, S H
Publicat 1986

Organisation of the human PAX4 gene and its exclusion as a candidate for the Wolcott-Rallison syndrome.

per Bonthron, D T, Dunlop, N, Barr, D G, El Sanousi, A A, Al-Gazali, L I
Publicat 1998

Platelet-derived growth factor A-chain gene transcription is mediated by positive and negative regulatory regions in the promoter.

per Kaetzel, D M, Maul, R S, Liu, B, Bonthron, D, Fenstermaker, R A, Coyne, D W
Publicat 1994

A locus for isolated cleft palate, located on human chromosome 2q32.

per Brewer, C M, Leek, J P, Green, A J, Holloway, S, Bonthron, D T, Markham, A F, FitzPatrick, D R
Publicat 1999

Mutations in the AP1S2 gene encoding the sigma 2 subunit of the adaptor protein 1 complex are associated with syndromic X‐linked mental retardation with hydrocephalus and calcifica...

per Saillour, Y, Zanni, G, Portes, V Des, Heron, D, Guibaud, L, Iba‐Zizen, M T, Pedespan, J L, Poirier, K, Castelnau, L, Julien, C, Franconnet, C, Bonthron, D, Porteous, M E, Chelly, J, Bienvenu, T
Publicat 2007