Connecting you to content on EBSCOhost

Works matching IS 00034800 AND DT 1998 AND VI 62 AND IP 3

Results: 5

1

Genetic mapping of disease genes. Edited by I-H. PAWLOWITZKI, J. H. EDWARDS and E. A. THOMPSON. London: Academic Press. 1997. Pp. 288. £45.00.

Published in:

Annals of Human Genetics, 1998, v. 62, n. 3, p. 275, doi. 10.1046/j.1469-1809.1998.6230275.x

By:

CURTIS, D.

Publication type:

Article

2

Phylogeography of mitochondrial DNA in western Europe.

Published in:

Annals of Human Genetics, 1998, v. 62, n. 3, p. 241, doi. 10.1046/j.1469-1809.1998.6230241.x

By:

RICHARDS, M. B.;
MACAULAY, V. A.;
BANDELT, H.-J.;
SYKES, B. C.

Publication type:

Article

3

C73R is a hotspot mutation in the uroporphyrinogen III synthase gene in congenital erythropoietic porphyria.

Published in:

Annals of Human Genetics, 1998, v. 62, n. 3, p. 225, doi. 10.1046/j.1469-1809.1998.6230225.x

By:

FRANK, J.;
WANG, X.;
LAM, H-M.;
AITA, V. M.;
JUGERT, F. K.;
GOERZ, G.;
MERK, H. F.;
POH-FITZPATRICK, M. B.;
CHRISTIANO, A. M.

Publication type:

Article

4

Lactase haplotype frequencies in Caucasians: association with the lactase persistence/non-persistence polymorphism.

Published in:

Annals of Human Genetics, 1998, v. 62, n. 3, p. 215, doi. 10.1046/j.1469-1809.1998.6230215.x

By:

HARVEY, C. B.;
HOLLOX, E. J.;
POULTER, M.;
WANG, Y.;
ROSSI, M.;
AURICCHIO, S.;
IQBAL, T. H.;
COOPER, B. T.;
BARTON, R.;
SARNER, M.;
KORPELA, R.;
SWALLOW, D. M.

Publication type:

Article

5

A mutation screen of the TSC1 gene reveals 26 protein truncating mutations and 1 splice site mutation in a panel of 79 tuberous sclerosis patients.

Published in:

Annals of Human Genetics, 1998, v. 62, n. 3, p. 203, doi. 10.1046/j.1469-1809.1998.6230203.x

By:

YOUNG, J. M.;
BURLEY, M. W.;
JEREMIAH, S. J.;
JEGANATHAN, D.;
EKONG, R.;
OSBORNE, J. P.;
POVEY, S.

Publication type:

Article