Evaluation of methylation analysis for diagnostic testing in 258 referrals suspected of Prader-Willi or Angelman syndromes Tina BuchholzJulianne JacksonA. Smith Original investigation Pages: 535 - 539
Transmission disequilibrium and sequence variants at the leptin receptor gene in extremely obese German children and adolescents H. RothTina KornKarl-Heinz Grzeschik Original investigation Pages: 540 - 546
Confirmation of FWT1 as a Wilms’ tumour susceptibility gene and phenotypic characteristics of Wilms’ tumour attributable to FWT1 N. RahmanFatima AbidiMichael R. Stratton Original investigation Pages: 547 - 556
The nuclear-encoded human NADH:ubiquinone oxidoreductase NDUFA8 subunit: cDNA cloning, chromosomal localization, tissue distribution, and mutation detection in complex-I-deficient patients Ralf TriepelsL. van den HeuvelJan Smeitink Original investigation Pages: 557 - 563
Mitotic and meiotic instability of the CAG trinucleotide repeat in spinocerebellar ataxia type 1 Pernille KoefoedL. HasholtSven Asger Sørensen Original investigation Pages: 564 - 569
Exon 1 donor splice site mutations in the porphobilinogen deaminase gene in the non-erythroid variant form of acute intermittent porphyria Hervé PuyUlrich GroßManfred Doss Original investigation Pages: 570 - 575
Change of bone mass in postmenopausal Caucasian women with and without hormone replacement therapy is associated with vitamin D receptor and estrogen receptor genotypes H.-W. DengJian LiRobert R. Recker Original investigation Pages: 576 - 585
Alteration of the LIS1 gene in Japanese patients with isolated lissencephaly sequence or Miller-Dieker syndrome M. SakamotoJiro OnoHiroki Kurahashi Original Investigation Pages: 586 - 589
Complete physical map of the common deletion region in Williams syndrome and identification and characterization of three novel genes X. MengXiaojun LuMark T. Keating Original investigation Pages: 590 - 599
Neurofibromatosis pseudogene amplification underlies euchromatic cytogenetic duplications and triplications of proximal 15q J. C. K. BarberI. E. CrossCaroline E. Browne Original investigation Pages: 600 - 607
Association of infantile convulsions with paroxysmal dyskinesias (ICCA syndrome): confirmation of linkage to human chromosome 16p12-q12 in a Chinese family Wei-Ling LeeA. TayPierre Szepetowski Original investigation Pages: 608 - 612
Molecular characterization of phenylketonuria in Japanese patients Y. OkanoMinoru AsadaGen Isshiki Original investigation Pages: 613 - 618
Identification of de novo chromosomal markers and derivatives by spectral karyotyping B. R. HaddadEvelin SchröckThomas Ried Original investigation Pages: 619 - 625
FRAXE : the HindIII/OXE20 restriction polymorphism is not a rare variant M. BlayauSylvie OdentVéronique David Letter to the editor Pages: 626 - 627
The origins of Native Americans: evidence from anthropological genetics: Michael H. Crawford Cambridge University Press (308 pages), ISBN 0-521-59280-1, US $ 64.95, Hardcover Derek F. Roberts Book review Pages: 628 - 629
Principles of molecular medicine: J. Larry Jameson (Editor) Humana Press (1156 pages), ISBN 0-896-03529-8, US $175, Hardcover N. Haites Book review Pages: 630 - 630
Mental disorders and genetics: the ethical context. Nuffield Council on Bioethics – 1998 Nuffield Council on Bioethics, 28 Bedford Square, London WC 1 3EG, UK (http:/www.nuffield.org),(117 pages), ISBN 0-9522701-3-7, GB £20 plus postage, from publisher P. Harper Book review Pages: 631 - 631