Increased rate of nondisjunction in sex cells derived from low-quality semen Sharona FinkelsteinE. MukamelL. Avivi Original investigation Pages: 129 - 137
Inheritance of chronic tension-type headache investigated by complex segregation analysis Michael Bjørn RussellLennart IseliusJes Olesen Original investigation Pages: 138 - 140
DNA polymorphisms and haplotypes in the human transferrin gene L. E. BeckmanG. F. Van LandeghemL. Beckman Original investigation Pages: 141 - 144
The mutations in FGFR2-associated craniosynostoses are clustered in five structural elements of immunoglobulin-like domain III of the receptor Daniela SteinbergerGert VriendU. Müller Original investigation Pages: 145 - 150
Failure of testicular development associated with a rearrangement of 9p24.1 proximal to the SNF2 gene Ruxandra IonL. TelviKen McElreavey Original investigation Pages: 151 - 156
Detection of structural abnormalities in spermatozoa of a translocation carrier t(3;11)(q27.3;q24.3) by triple FISH E. MartiniA. R. M. von BerghJ. P. M. Geraedts Original investigation Pages: 157 - 165
Retroviral gene transfer for the assignment of Fanconi anemia (FA) patients to a FA complementation group Kai-Ling FuPeter C. ThußChristopher E. Walsh Original investigation Pages: 166 - 169
Molecular genetic analysis of patients carrying steroid 21-hydroxylase deficiency in the Mexican population: identification of possible new mutations and high prevalence of apparent germ-line mutations Maria Luisa Ordoñez-SánchezSalvador Ramírez-JiménezM. T. Tusié-Luna Original investigation Pages: 170 - 177
Refined localisation of the voltage-gated chloride channel, CLCN3, to 4q33 Laurence TaineIsabelle CoupryBenoît Arveiler Original investigation Pages: 178 - 181
Transmission of mitochondrial DNA heteroplasmy in normal pedigrees Christopher D. GockeFloyd A. BenkoP. K. Rogan Original investigation Pages: 182 - 186
A double missense mutation in the ATM gene of a Dutch family with ataxia telangiectasia M. J. van BelzenJohan A. P. HielL. P. W. J. van den Heuvel Original investigation Pages: 187 - 191
Structure of the human amyloid-precursor-like protein gene APLP1 at 19q13.1 Ulla LenkkeriMarjo KestiläKarl Tryggvason Original investigation Pages: 192 - 196
A germline mutation abolishing the original stop codon of the human adenine phosphoribosyltransferase (APRT) gene leads to complete loss of the enzyme protein Atsuo TaniguchiMasayuki HakodaN. Kamatani Original investigation Pages: 197 - 202
Localization of the gene responsible for Peutz-Jeghers syndrome within a 6-cM region of chromosome 19p13.3 Hidewaki NakagawaKumiko KoyamaYusuke Nakamura Original investigation Pages: 203 - 206
Quantitative DNA pooling to increase the efficiency of linkage analysis in autosomal dominant disease K. F. DamjiC. J. GallioneD. A. Marchuk Original investigation Pages: 207 - 212
A novel missense mutation (S18N) in the 5′ non-HMG box region of the SRY gene in a patient with partial gonadal dysgenesis and his normal male relatives Sorahia DomeniceMiriam Yumie NishiB. Bilharinho Mendonca Original investigation Pages: 213 - 215
Novel and recurrent mutations in the PKD1 (Polycystic Kidney disease) gene C. DaniellsMagitha MaheshwarDavid Ravine Original investigation Pages: 216 - 220
Localisation of receptor interacting protein140 (RIP140) within 100kb of D21S13 on 21q11, a gene-poor region of the human genome Nicholas KatsanisJane H. IvesE. M. C. Fisher Original investigation Pages: 221 - 223
Analysis of the CFTR gene in Turkish cystic fibrosis patients: identification of three novel mutations (3172delAC, P1013L and M1028I) T. OnayO. TopalogluB. Kirdar Original investigation Pages: 224 - 230
Polarity of mutations in tumor-associated microsatellite instability Rosane SturzenekerLuciana A. HaddadSérgio D. J. Pena Original investigation Pages: 231 - 235
Linkage between atopy and the IgE high-affinity receptor gene at 11q13 in atopic dermatitis families R. Fölster-HolstHans W. MoisesEnno Christophers Original investigation Pages: 236 - 239
Structure and dynamics of human interphase chromosome territories in vivo D. ZinkT. CremerErnst H. K. Stelzer Rapid communication Pages: 241 - 251
Gene Symbol: NF2 Disease: Neurofibromatosis 2 C. EhlersR. Fahsold Human gene mutations Pages: 252 - 252