Parental origin of transcription from the human GNAS1 gene.

Yazar: Campbell, R, Gosden, C M, Bonthron, D T
Baskı/Yayın Bilgisi 1994

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

Yazar: Jouet, M, Strain, L, Bonthron, D, Kenwrick, S
Baskı/Yayın Bilgisi 1996

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

Yazar: Strain, L, Wright, A F, Bonthron, D T
Baskı/Yayın Bilgisi 1997

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

Yazar: Bonthron, D T, Morton, C C, Orkin, S H, Collins, T
Baskı/Yayın Bilgisi 1988

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

Yazar: Strain, L., Bonthron, D.T., Brock, D.J.H.
Baskı/Yayın Bilgisi 1991

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

Yazar: Bonthron, D T, Markham, A F, Ginsburg, D, Orkin, S H
Baskı/Yayın Bilgisi 1985

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

Yazar: Bonthron, D T, Smith, S J, Fantes, J, Gosden, C M
Baskı/Yayın Bilgisi 1993

PMS2 mutations in childhood cancer

Yazar: Bonthron, D T, Hayward, B E, De Vos, M, Sheridan, E
Baskı/Yayın Bilgisi 2005

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

Yazar: Strain, L., Gosden, C. M., Brock, D. J., Bonthron, D. T.
Baskı/Yayın Bilgisi 1994

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

Yazar: Bonthron, D T, Barlow, K M, Burt, A M, Barr, D G
Baskı/Yayın Bilgisi 1993

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

Yazar: Resnick, N, Collins, T, Atkinson, W, Bonthron, D T, Dewey, C F, Gimbrone, M A
Baskı/Yayın Bilgisi 1993

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

Yazar: Resnick, N, Collins, T, Atkinson, W, Bonthron, D T, Dewey, C F, Gimbron, M A
Baskı/Yayın Bilgisi 1993

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

Yazar: Brickwood, S, Bonthron, D, Al-Gazali, L, Piper, K, Hearn, T, Wilson, D, Hanley, N
Baskı/Yayın Bilgisi 2003

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

Yazar: Gashler, A L, Bonthron, D T, Madden, S L, Rauscher, F J, Collins, T, Sukhatme, V P
Baskı/Yayın Bilgisi 1992

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

Yazar: Bonthron, D, Orr, E C, Mitsock, L M, Ginsburg, D, Handin, R I, Orkin, S H
Baskı/Yayın Bilgisi 1986

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

Yazar: Bonthron, D T, Dunlop, N, Barr, D G, El Sanousi, A A, Al-Gazali, L I
Baskı/Yayın Bilgisi 1998

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

Yazar: Kaetzel, D M, Maul, R S, Liu, B, Bonthron, D, Fenstermaker, R A, Coyne, D W
Baskı/Yayın Bilgisi 1994

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

Yazar: Brewer, C M, Leek, J P, Green, A J, Holloway, S, Bonthron, D T, Markham, A F, FitzPatrick, D R
Baskı/Yayın Bilgisi 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...

Yazar: 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
Baskı/Yayın Bilgisi 2007