Clinical Genetics

Consanguinity and its relevance to clinical genetics
pp. 89-98(10)
Author: Bittles, AH

HotSpots
pp. 99-100(2)
Authors: Devon, Rebecca S; Chopra, Vikramjit; van Raamsdonk, Jeremy M

HotSpots
pp. 100-102(3)
Authors: Devon, Rebecca S; Chopra, Vikramjit; van Raamsdonk, Jeremy M

HotSpots
pp. 102-103(2)
Authors: Devon, Rebecca S; Chopra, Vikramjit; van Raamsdonk, Jeremy M

History of genetics through philately - Carl Linnaeus (Carl von Linné)
pp. 104-106(3)
Author: Chudley, Albert E

The additive effect of neurotransmitter genes in pathological gambling
pp. 107-116(10)
Authors: Comings, DE; Gade-Andavolu, R; Gonzalez, N; Wu, S; Muhleman, D; Chen, C; Koh, P; Farwell, K; Blake, H; Dietz, G; MacMurray, JP; Lesieur, HR; Rugle, LJ; Rosenthal, RJ

Determination of a positive malignant hyperthermia (MH) disposition without the in vitro contracture test in families carrying the RYR1 Arg614Cys mutation
pp. 117-124(8)
Authors: Rueffert, H; Olthoff, D; Deutrich, C; Froster, UG

Phenotype variability of two FAP families with an identical APC germline mutation at codon 1465: a potential modifier effect?
pp. 125-131(7)
Authors: Martin-Denavit, T; Duthel, S; Giraud, S; Olschwang, S; Saurin, JC; Plauchu, H

Apolipoprotein E polymorphism and lipid levels differ by gender and family history of diabetes: the Rancho Bernardo Study
pp. 132-137(6)
Authors: Oh, J-Y; Barrett-Connor, E

Genetic heterogeneity in Korean families with autosomal-dominant polycystic kidney disease (ADPKD): the first Asian report
pp. 138-144(7)
Authors: Lee, Jung Geon; Lee, Kyu Beck; Kim, Un Kyung; Ahn, Curie; Hwang, Dae Yeon; Hwang, Young Hwan; Eo, Hyun-Seon; Lee, Eun Joo; Kim, Yon Su; Han, Jin Suk; Kim, Suhnggwon; Lee, Jung Sang

Quantification of all fetal nucleated cells in maternal blood between the 18th and 22nd weeks of pregnancy using molecular cytogenetic techniques
pp. 145-150(6)
Authors: Krabchi, K; Gros-Louis, F; Yan, J; Bronsard, M; Massé, J; Forest, J-C; Drouin, R

PAX6 mutation in a family with aniridia, congenital ptosis, and mental retardation
pp. 151-154(4)
Authors: Malandrini, A; Mari, F; Palmeri, S; Gambelli, S; Berti, G; Bruttini, M; Bardelli, AM; Williamson, K; van Heyningen, V; Renieri, A

Further evidence for linkage of low-mid frequency hearing impairment to the candidate region on chromosome 4p16.3
pp. 155-160(6)
Authors: Brodwolf, S; Böddeker, IR; Ziegler, A; Rausch, P; Kunz, J

Molecular genetic analysis of the cystathionine β-synthase gene in Portuguese homocystinuria patients: three novel mutations
pp. 161-163(3)
Authors: Castro, R; Heil, SG; Rivera, I; Jakobs, C; de Almeida, IT; Blom, HJ