Identifying chromosomal fragile sites from individuals: a multinomial statistical model Udo BöhmP. Frederick DahmIra F. Greenbaum Original Investigation Pages: 249 - 256
Mucopolysaccharidosis IVA: polymorphic haplotypes and informative RFLPs in the Japanese population Hideki IwataShunji TomatsuTadao Orii Original Investigation Pages: 257 - 264
Chromosomal localization of the human NF-E2 family of bZIP transcription factors by fluorescence in situ hybridization Jefferson Y. ChanMei-Chi CheungYuet Wai Kan Original Investigation Pages: 265 - 269
Somatic expansion of the (CAG) n repeat in Huntington disease brains Karien E. De RooijPia A. M. De Koning GansJohan T. Den Dunnen Original Investigation Pages: 270 - 274
Sequence polymorphism in kringle IV 37 in linkage disequilibrium with the apolipoprotein (a) size polymorphism H. G. KraftC. HaibachG. Utermann Original Investigation Pages: 275 - 282
Deletion mapping of stature determinants on the long arm of the Y chromosome Pia SaloHelena KääriäinenAlbert de la Chapelle Original Investigation Pages: 283 - 286
Analysis of pericentromeric chromosome 21 specific YAC clones by FISH: Identification of new markers for molecular-cytogenetic application Yuri B. YurovAnne-Marie LaurentGerard Roizes Original Investigation Pages: 287 - 292
Interphase cytogenetics on paraffin-embedded sections of ovary for detection of genomic constitution in a patient with Turner's syndrome and chromosomal mosaicism Angelina Z. NovakGeorge K. KokaiVladimir A. Jurukovski Original Investigation Pages: 293 - 298
Analysis of a whole arm translocation between chromosomes 18 and 20 using fluorescence in situ hybridization: detection of a break in the centromeric α-satellite sequences Zeynep TümerAnna BergMargareta Mikkelsen Original Investigation Pages: 299 - 302
The breakpoint on 7p in a patient with t(6;7) and craniosynostosis is spanned by a YAC clone containing the D7S503 locus Kazushiro TsujiKouji NaraharaJürgen Kunz Original Investigation Pages: 303 - 307
Transthyretin Ser 6 gene frequency in individuals without amyloidosis Daniel R. JacobsonIsabel L. AlvesJoel N. Buxbaum Original Investigation Pages: 308 - 312
Elongated CAG repeats of the B37 gene in a Danish family with dentato-rubro-pallido-luysian atrophy A. NørremølleJ. E. NielsenL. Hasholt Original Investigation Pages: 313 - 318
Variability of the immunoglobulin heavy chain constant region locus: a population study Alfredo BruscoUmberto CariotaAngelo O. Carbonara Original Investigation Pages: 319 - 326
Asp187Asn mutation of gelsolin in an American kindred with familial amyloidosis, Finnish type (FAP IV) Robert D. SteinerJames P. EvansMerrill D. Benson Original Investigation Pages: 327 - 330
Clinical characteristics of 16 cystic fibrosis patients with the missense mutation R334W, a pancreatic insufficiency mutation with variable age of onset and interfamilial clinical differences X. EstivillR. LlevadotC. Vázquez Original Investigation Pages: 331 - 336
An inactive cytochrome P450 CYP2D6 allele containing a deletion and a base substitution Ann K. DalyJulian B. S. LeathartStephanie J. London Original Investigation Pages: 337 - 341
Refinement of the X-linked cleft palate and ankyloglossia (CPX) localisation by genetic mapping in an Icelandic kindred S. A. ForbesM. RichardsonL. Campbell Original Investigation Pages: 342 - 346
Somatic mutations in the neurofibromatosis type 2 gene in sporadic meningiomas Laura PapiLucia Rosaria De VitisPasquale Mennonna Original Investigation Pages: 347 - 351
Population study of a sequence polymorphism in intron 2 of the human β-globin gene A. BraunH. AmbachS. Kammerer Short Communication Pages: 352 - 352
Linkage disequilibrium between a SacI restriction fragment length polymorphism and two galactosemia mutations Hsien-Chin LinJuergen K. V. Reichardt Short Communication Pages: 353 - 355
Localization of the human soluble epoxide hydrolase gene (EPHX2) to chromosomal region 8p21-p12 Catharina LarssonIrene WhiteJohan Meijer Short Communication Pages: 356 - 358
SpαI/65 hereditary elliptocytosis in Calabria (southern Italy) A. QualtieriM. G. BisconteC. Brancati Short Communication Pages: 359 - 362
A new restriction-site polymorphism in exon 18 of the low density lipoprotein receptor (LDLR) gene David H. KassMark A. BatzerPrescott L. Deininger OriginalPaper Pages: 363 - 364
A TaqI polymorphism in the human erythroid β spectrin gene L. BeetonJ. T. PrchalT. L. Coetzer OriginalPaper Pages: 365 - 366
Identification of two highly polymorphic CA-repeats (D21S1224 and D21S1261) on human chromosome 21q22.3 Assumpció BoschJordi GuimeràXavier Estivill OriginalPaper Pages: 367 - 369