J. Lynch

发表

Genomic organization of the sequence coding for fibrillin, the defective gene product in Marfan syndrome.

B. Sykes, J. Bonadio, M. D’Alessio, 1993, Human molecular genetics.

A molecular approach to the stratification of cardiovascular risk in families with Marfan's syndrome.

H. Dietz, R. Pyeritz, B. Sykes, 1994, The New England journal of medicine.

Confirmation of genetic linkage between atopic IgE responses and chromosome 11q13.

G. Lathrop, W. Cookson, G. Lathrop, 1992, Journal of medical genetics.

Direct detection of haemoglobin E with MnlI.

D. Weatherall, S. Thein, J. Old, 1987, Journal of medical genetics.

Genomic organization of the sequence coding for fibrillin, the defective gene product in Marfan syndrome.

B. Sykes, J. Bonadio, M. D’Alessio, 1993, Human molecular genetics.

A new missense mutation of fibrillin in a patient with Marfan syndrome.

B. Sykes, A. Child, D. Hewett, 1994, Journal of Medical Genetics.

DIRECT DETECTION OF β°39 THALASSAEMIC MUTATION WITH Mae 1

D. Weatherall, S. Thein, J. Wainscoat, 1985, The Lancet.

PCR detection of five restriction site dimorphisms at the type I collagen loci COL1A1 and COL1A2.

B. Sykes, J. Lynch, L. Ferguson, 1991, Nucleic acids research.

Genetic analysis in cystic fibrosis

A. Markham, D. Ogilvie, C. Newton, 2022 .

Evolutionary relationships of human populations from an analysis of nuclear DNA polymorphisms

A. Hill, J. Flint, J. Clegg, 1986, Nature.

Prenatal diagnosis of osteogenesis imperfecta by identification of the concordant collagen 1 allele.

B. Sykes, D. Ogilvie, P. Farndon, 1991, Journal of medical genetics.

The polymerase chain reaction: current and future clinical applications.

Jennifer M. Brown, J. Lynch, J. Brown, 1990, Journal of medical genetics.

Thepolymerase chainreaction: currentandfuture clinical applications

Jennifer M. Brown, J. Lynch, 1990 .

Prenatal diagnosis and linkage disequilibrium with cystic fibrosis for markers surrounding D7S8

F. Collins, M. Iannuzzi, B. Weir, 1990, Human Genetics.

A novel fibrillin mutation in the Marfan syndrome which could disrupt calcium binding of the epidermal growth factor-like module.

B. Sykes, D. Hewett, J. Lynch, 1993, Human molecular genetics.

Differential allelic expression of a fibrillin gene (FBN1) in patients with Marfan syndrome.

H. Firth, B. Sykes, A. Child, 1994, American journal of human genetics.

Characterization of the breakpoint of a 3.5-kb deletion of the β-globin gene

D. Weatherall, S. Best, Jennifer M. Brown, 1991 .

Characterization of the breakpoint of a 3.5-kb deletion of the beta-globin gene.

D. Weatherall, S. Best, J. Lynch, 1991, Genomics.

DIRECT DETECTION OF HAEMOGLOBIN E WITH SYNTHETIC OLIGONUCLEOTIDES

D. Weatherall, S. Thein, R. B. Wallace, 1986, The Lancet.

Genetic analysis in cystic fibrosis using the amplification refractory mutation system (ARMS): the J3.11 MspI polymorphism.

A. Markham, D. Ogilvie, C. Newton, 1991, Journal of medical genetics.