Clinical Genetics

Sib-pairs in multifactorial disorders: the sib-similarity problem
pp. 1-9(9)
Author: Edwards J.

Hotspots
pp. 10-11(2)
Author: Nasir J.

Hotspots
pp. 11-12(2)
Author: Nasir J.

Hotspots
pp. 13-14(2)
Author: Nasir J.

Genetic technologies, health care policy and the patent bargain
pp. 15-18(4)
Authors: Caulfield T.; Knoppers B.; Gold E.; Sheremeta L.; Bridge P.

The TaqIB and -629C>A polymorphisms at the cholesteryl ester transfer protein locus: associations with lipid levels in a multiethnic population. The 1998 Singapore National Health Survey
pp. 19-30(12)
Authors: Tai E.; Ordovas J.; Corella D.; Deurenberg-Yap M.; Chan E.; Adiconis X.; Chew S.; Loh L.; Tan C.

The association of cholesteryl ester transfer protein polymorphism with high-density lipoprotein cholesterol and coronary artery disease in Koreans
pp. 31-38(8)
Authors: Park K-W.; Choi J-H.; Kim H-K.; Oh S.; Chae I-H.; Kim H-S.; Oh B-H.; Lee M-M.; Park Y-B.; Choi Y-S.

A second kindred linked to DFNA20 (17q25.3) reduces the genetic interval
pp. 39-45(7)
Authors: DeWan A.; Parrado A.; Leal S.

Fabry disease: a functional and anatomical study of cardiac manifestations in 20 hemizygous male patients
pp. 46-52(7)
Authors: Senechal M.; Germain D.

Polymorphisms at the SRBI locus are associated with lipoprotein levels in subjects with heterozygous familial hypercholesterolemia
pp. 53-58(6)
Authors: Tai E.; Adiconis X.; Ordovas J.; Carmena-Ramon R.; Real J.; Corella D.; Ascaso J.; Carmena R.

A novel point mutation of the androgen receptor (F804L) in an Egyptian newborn with complete androgen insensitivity associated with congenital glaucoma and hypertrophic pyloric stenosis
pp. 59-63(5)
Authors: Gad Y.; Mazen I.; Lumbroso S.; Temtamy S.; Sultan C.

Very low incidence of microsatellite instability in rectal cancers from families at risk for HNPCC
pp. 64-70(7)
Authors: Hoogerbrugge N.; Willems R.; van Krieken H.; Kiemeney L.; Weijmans M.; Nagengast F.; Arts N.; Brunner H.; Ligtenberg M.

A predominant increase in the APC gene isoform with exon 9a in a case of attenuated familial adenomatous polyposis
pp. 71-72(2)

PROMM and deafness: exclusion of ZNF9 as the disease gene in DFNA18 suggests a polygenic origin of the PROMM/DM2 phenotype
pp. 73-75(3)

A case of de novo distal duplication of chromosome 15
pp. 76-78(3)

‘Severe’ Prader–Willi syndrome with a large deletion of chromosome 15 due to an unbalanced t(15,22)(q14;q11.2) translocation
pp. 79-81(3)

“GENETICS AND HEALTH CARE”: CALL FOR ABSTRACTS
pp. 82-82(1)