ACP1 and human adaptability 1. Association with common diseases: a case-control study E. BottiniF. Gloria-BottiniP. Borgiani Original Investigation Pages: 629 - 637
Genotype-phenotype correlation in a series of 167 deletion and non-deletion patients with Prader-Willi syndrome Gabriele Gillessen-KaesbachWendy RobinsonBernhard Horsthemke Original Investigation Pages: 638 - 643
Detection of chromosome aberrations in paraffin sections of seven gonadal yolk sac tumors of childhood Jutta JendernyEckhard KösterUte Jänig Original Investigation Pages: 644 - 650
Proliferation enhancement by spontaneous multiplication of chromosome 7 in rheumatic synovial cells in vitro Ayhan ErmisWolfram HennKlaus D. Zang Original Investigation Pages: 651 - 654
Sperm nuclei analysis of a Robertsonian t(14q21q) carrier, by FISH, using three plasmids and two YAC probes Sophie RousseauxEdith ChevretBernard Sèle Original Investigation Pages: 655 - 660
Complete and precise characterization of marker chromosomes by application of microdissection in prenatal diagnosis Jutta Müller-NaviaAlmut NebelEngelhardt Schleiermacher Original Investigation Pages: 661 - 667
Localization of the CDKN4/p27Kip1 gene to human chromosome 12p12.3 Emmanuel MartinValère CacheuxBernard Grandchamp Original Investigation Pages: 668 - 670
Human glial cell line-derived neurotrophic factor (GDNF) maps to chromosome 5 Nessan BerminghamRenate HillermannElizabeth M. C. Fisher Original Investigation Pages: 671 - 673
Selection against blood cells deficient in hypoxanthine phosphoribosyltransferase (HPRT) in Lesch-Nyhan heterozygotes occurs at the level of multipotent stem cells Masayuki HakodaYuko HiraiSadao Kashiwazaki Original Investigation Pages: 674 - 680
Three novel mutations in the interleukin-2 receptor γ chain gene in four Japanese patients with X-linked severe combined immunodeficiency Yoshiyuki MinegishiNaoto IshiiJun-ichi Yata Original Investigation Pages: 681 - 683
Chromosome 17 abnormalities and lack of TP53 mutations in paediatric central nervous system tumours Catherine M. PhelanLu LiuVincent P. Collins Original Investigation Pages: 684 - 690
Refinement by linkage analysis in two large families of the candidate region of the third locus (SCA3) for autosomal dominant cerebellar ataxia type I Corien C. Verschuuren-BemelmansEwout R. P. BruntHans Scheffer Original Investigation Pages: 691 - 694
Parental generalized EEG alpha activity predisposes to spike wave discharges in offspring Hermann DooseEva CastiglioneStephan Waltz Original Investigation Pages: 695 - 704
APC mutation in the alternatively spliced region of exon 9 associated with late onset familial adenomatous polyposis Rob B. van der LuijtHans F. A. VasenP. Meera Khan Original Investigation Pages: 705 - 710
Germline mosaicism for an alanine to valine substitution at residue β 140 in hemoglobin Puttelange, a new variant with high oxygen affinity H. WajcmanE. GirodonF. Galacteros Original Investigation Pages: 711 - 716
Four adult patients with the missense mutation L206W and a mild cystic fibrosis phenotype Marie DesgeorgesMichel RodierMireille Claustres Original Investigation Pages: 717 - 720
Characterization of two stop codon mutations in the galactose-1-phosphate uridyltransferase gene of three male galactosemic patients with severe clinical manifestation B. S. GathofM. SommerY. S. Shin Original Investigation Pages: 721 - 725
Inheritance of migraine investigated by complex segregation analysis Michael Bjørn RussellLennart IseliusJes Olesen Original Investigation Pages: 726 - 730
No evidence of genetic heterogeneity in Crouzon craniofacial dysostosis Hong Wi MaElisabeth LajeunieDominique Renier Original Investigation Pages: 731 - 735
Dinucleotide repeat polymorphism in the human ceruloplasmin gene Makoto DaimonYoshihiro MoritaHideo Sasaki OriginalPaper Pages: 736 - 736
Polymorphic tri and tetranucleotide repeats in exons 1 and 8 of the myelin oligodendrocyte glycoprotein (MOG) gene L. MalfroyC. ViratelleM. P. Roth OriginalPaper Pages: 737 - 738
Single nucleotide polymorphisms in the human E-cadherin gene Karl-Friedrich BeckerUlrike ReichHeinz Höfler OriginalPaper Pages: 739 - 740
Polymorphism in the 3′ untranslated region of the phenylalanine hydroxylase gene detected by enzyme mismatch cleavage: evolution of haplotypes Susan J. RamusRichard G. H. Cotton OriginalPaper Pages: 741 - 743
A Tsp509I variant in exon 13 of the neurofibromatosis type 1 (NF1) gene allows the identification of both alleles at the mRNA level Vinciane RégnierGisèle DanglotAlain Bernheim Erratum Pages: 744 - 744