B. Farren

发表

Confirmation of an association between RFLPs at the transforming growth factor-alpha locus and non-syndromic cleft lip and palate.

R. Winter, S. Holder, S. Malcolm, 1992, Journal of medical genetics.

Corrigendum: Clinical studies of multiple endocrine neoplasia type 1 (MEN1) (Q J Med (1996) 89 (653-659))

C. Edwards, R. Thakker, J. Sampson, 1996 .

Defects of insulin action on fatty acid and carbohydrate metabolism in familial combined hyperlipidemia.

T. Aitman, D. Crook, J. Scott, 1997, Arteriosclerosis, thrombosis, and vascular biology.

Duplications of proximal 16q flanked by heterochromatin are not euchromatic variants and show no evidence of heterochromatic position effect

V. Maloney, J. Barber, A. Barnicoat, 2006, Cytogenetic and Genome Research.

Interaction of cytochrome c with mixed dimyristoylphosphatidylcholine-dimyristoylphosphatidylserine bilayers: a deuterium nuclear magnetic resonance study.

A. MacKay, G. Hoatson, P. Devaux, 1986, Biochemistry.

Clinical studies of multiple endocrine neoplasia type 1 (MEN1)

C. Edwards, R. Thakker, J. Sampson, 1996, QJM : monthly journal of the Association of Physicians.

Genetic mapping studies of 40 loci and 23 cosmids in chromosome 11p13-11g13, and exclusion of μ-calpain as the multiple endocrine neoplasia type 1 gene

B. Harding, R. Thakker, M. Pook, 1996, Human Genetics.

Mutations in SNX14 cause a distinctive autosomal-recessive cerebellar ataxia and intellectual disability syndrome.

M. Bitner-Glindzicz, F. Baas, H. Williams, 2014, American journal of human genetics.

Familial combined hyperlipidaemia linked to the apolipoprotein AI–CIII–AIV gene cluster on chromosome 11q23q–q24

M. Farrall, P. Cullen, C. Packard, 1991, Nature.

Complex segregation analysis provides evidence for a major gene acting on serum triglyceride levels in 55 British families with familial combined hyperlipidemia.

M. Farrall, P. Cullen, J. Scott, 1994, Arteriosclerosis and thrombosis : a journal of vascular biology.

Linkage analysis of 7 polymorphic markers at chromosome 11p11. 2‐11q13 in 27 multiple endocrine neoplasia type 1 families

P. Woollard, R. Norum, B. Harding, 1993, Annals of human genetics.

Oculodentodigital dysplasia and type III syndactyly: separate genetic entities or disease spectrum?

R. Winter, S. Huson, L. Brueton, 1990, Journal of medical genetics.

Oculodentodigital dysplasia and type III syndactyly: separate genetic entities or disease spectrum?

B. Farren, Louise Brueton, S. M. Huson, 1990, Journal of medical genetics.