Distribution of glucose-6-phosphate dehydrogenase mutations in Southeast Asia Kuni IwaiAkira HironoAkira Ishii Original Investigation 12 June 2001 Pages: 445 - 449
Evaluation of the fragile X (FRAXA) syndrome with methylation-sensitive PCR Andreas WeinhäuselOskar A. Haas Original Investigation 06 June 2001 Pages: 450 - 458
Analyses of genetic abnormalities in type I CD36 deficiency in Japan: identification and cell biological characterization of two novel mutations that cause CD36 deficiency in man Hirokazu KashiwagiYoshiaki TomiyamaYuji Matsuzawa Original Investigation 24 May 2001 Pages: 459 - 466
The structure of duplications on human acrocentric chromosome short arms derived by the analysis of 15p I. PicciniL. BallaratiR. Meneveri Original Investigation 31 May 2001 Pages: 467 - 477
Improved definition of chromosomal breakpoints using high-resolution multicolour banding Johannes LemkeIlse ChudobaUwe Claussen Original Investigation 16 May 2001 Pages: 478 - 483
Statistical estimation and pedigree analysis ofCCR2-CCR5 haplotypes Vanessa J. ClarkNoah MethenyRaymond J. Peterson Original Investigation 19 May 2001 Pages: 484 - 493
Preimplantation genetic diagnosis for spinal and bulbar muscular atrophy (SBMA) Ioannis GeorgiouKaren SermonInge Liebaers Original investigation 31 May 2001 Pages: 494 - 498
Acrocentric chromosome disomy is increased in spermatozoa from fathers of Turner syndrome patients Sérgio SoaresFrancesca VidalCristina Templado Original Investigation 29 May 2001 Pages: 499 - 503
A 1.1-kb duplication in the p67-phox gene causes chronic granulomatous disease Lorena BorgatoAlberto BonizzatoRoberto Corrocher Original Investigation 02 June 2001 Pages: 504 - 510
Partial maternal heterodisomy of chromosome 17q25 in a case of severe mental retardation Marlène RioCatherine OzilouLaurence Colleaux Original Investigation 24 May 2001 Pages: 511 - 515
Interaction between the melanocortin-1 receptor andP genes contributes to inter-individual variation in skin pigmentation phenotypes in a Tibetan population Joshua M. AkeyHong WangLi Jin Original Investigation 06 June 2001 Pages: 516 - 520
Genome-wide distribution of linkage disequilibrium in the population of Palau and its implications for gene flow in Remote Oceania B. DevlinKathryn RoederW. Byerley Original Investigation 16 May 2001 Pages: 521 - 528
The genes for the human VPS10 domain-containing receptors are large and contain many small exons Wolfgang HampeMeriem RezgaouiChica H. Schaller Original Investigation 16 May 2001 Pages: 529 - 536
Physical and transcriptional mapping of the X-linked cleft palate and ankyloglossia (CPX) critical region Claire BraybrookGeorgina WarryPhilip Stanier Original Investigation 16 May 2001 Pages: 537 - 545
Analysis of lymphoedema-distichiasis families forFOXC2 mutations reveals small insertions and deletions throughout the gene R. BellG. BriceS. Jeffery Original Investigation 01 June 2001 Pages: 546 - 551
TheTNFRSF6 gene is not implicated in familial early-onset Alzheimer's disease Jessie TheunsLars FeukChristine Van Broeckhoven Short Report 16 May 2001 Pages: 552 - 553
Erratum to Back mutation can produce phenotype reversion in Bloom syndrome somatic cells Nathan A. EllisSusan CiocciJames German Erratum 23 May 2001 Pages: 554 - 554
Proteomics - from protein sequence to function Harry A. Dailey Book Review 16 May 2001 Pages: 555 - 555
Nigel M. Hooper (editor): Alzheimer’s disease. Methods and protocols Richard F. Cowburn Book Review 11 May 2001 Pages: 556 - 556
