Clinical Genetics

Multicultural education and genetic counseling
pp. 143-149(7)
Author: Weil J.

A few more pieces of the DM puzzle
pp. 150-152(6)
Author: Hackam A.S.

Silencing the quiet
pp. 152-153(6)
Author: Hackam A.S.

A phosphatase mutation implicated in multiple sclerosis
pp. 153-155(6)
Author: Hackam A.S.

The role of genomic imprinting in human developmental disorders: lessons from Prader–Willi syndrome
pp. 156-164(9)
Authors: Hanel M.; Wevrick R.

Shakespeare as a geneticist
pp. 165-170(6)
Author: Berg J.

Familial aggregation of QT-interval variability in a general population: results from the NHLBI Family Heart Study
pp. 171-177(7)
Authors: Hong Y.; Rautaharju P.; Hopkins P.; Arnett D.; Djoussé L.; Pankow J.; Sholinsky P.; Rao D.; Province M.

Identification of the Arg1086His mutation in the alpha subunit of the voltage-dependent calcium channel (CACNA1S) in a North American family with malignant hyperthermia
pp. 178-184(7)
Authors: Stewart S.; Hogan K.; Rosenberg H.; Fletcher J.

Novel molecular defects in the androgen receptor gene of Mexican patients with androgen insensitivity
pp. 185-188(4)
Authors: Chávez B.; Vilchis F.; Zenteno J.; Larrea F.; Kofman-Alfaro S.

Mutational screening of the cationic trypsinogen gene in a large cohort of subjects with idiopathic chronic pancreatitis
pp. 189-193(5)
Authors: Chen J.; Piepoli Bis A.; Le Bodic L.; Ruszniewski P.; Robaszkiewicz M.; Deprez P.; Raguenes O.; Quere I.; Andriulli A.; Ferec C.

Identification of novel C253Y missense and Y864X nonsense mutations in the insulin receptor gene in type A insulin-resistant patients
pp. 194-197(4)
Authors: Osawa H.; Nishimiya T.; Ochi M.; Niiya T.; Onuma H.; Kitamuro F.; Kaino Y.; Kida K.; Makino H.

Evidence for locus heterogeneity in the Camurati–Engelmann (DPD1) Syndrome
pp. 198-200(3)

The use of intragenic polymorphisms in determination of the genomic relevance of whole-exon deletions in MLH1 and MSH2
pp. 201-202(2)

Cenani–Lenz syndrome with renal hypoplasia is not linked to FORMIN or GREMLIN
pp. 203-205(3)