Duplication in the hypoxanthine phosphoribosyl-transferase gene caused by Alu-Alu recombination in a patient with Lesch Nyhan syndrome Suzanne MarcusDennis HellgrenJan Wahlström Original Investigations Pages: 477 - 482
Prenatal sex determination from maternal peripheral blood using the polymerase chain reaction Y. -M. Dennis LoPushpa PatelKenneth A. Fleming Original Investigations Pages: 483 - 488
Molecular study of chromosome 15 in 22 patients with Angelman syndrome Joke BeutenKathelijne MangelschotsPatrick J. Willems Original Investigations Pages: 489 - 495
Localization of the intronless gene coding for calmodulin-like protein CLP to human chromosome 10p13-ter M. W. BerchtoldM. KollerE. E. Strehler Original Investigations Pages: 496 - 500
Genetic linkage analysis of Canadian spinal muscular atrophy kindreds using flanking microsatellite 5q13 polymorphisms Alex MacKenzieNatalie RoyLinda Surh Original Investigations Pages: 501 - 504
Cloning and chromosome mapping of human retinoid X receptor β: selective amino acid sequence conservation of a nuclear hormone receptor in mammals K. FleischhauerO. W. McBrideS. Y. Yang Original Investigations Pages: 505 - 510
Decreased extracellular deposition of fibrillin and decorin in neonatal Marfan syndrome fibroblasts Michael RaghunathAndrea Superti-FurgaBeat Steinmann Original Investigations Pages: 511 - 515
A new polymorphic marker (D10S97) tightly linked to the multiple endocrine neoplasia type 2A (MEN2A) locus Jay B. LichterJingshi WuKenneth K. Kidd Original Investigations Pages: 516 - 520
Polymorphisms and linkage disequilibrium in the COL6A1 and COL6A2 gene cluster: novel DNA polymorphisms in the region of a candidate gene for congenital heart defects in Down's syndrome G. E. DaviesC. M. HowardA. M. Kessling Original Investigations Pages: 521 - 525
Molecular evaluation of an Alu repeat including a polymorphic variable poly(dA) (AluVpA) in the vitamin D binding protein (DBP) gene Andreas BraunRegina BichlmaierHartwig Cleve Original Investigations Pages: 526 - 532
Chromosomal analysis of unfertilized human oocytes prepared by a gradual fixation-air drying method Yujiroh KamiguchiBernd RosenbuschKazuya Mikamo Original Investigations Pages: 533 - 541
The human interleukin-6 receptor α chain gene is localized on chromosome 1 band q21 Petra M. C. KluckJoop WiegantJames E. Landegent Original Investigations Pages: 542 - 544
Linkage studies in Italian families with familial adenomatous polyposis Cristina MareniAlessandro StellaGinevra Guanti Original Investigations Pages: 545 - 550
X chromosome linkage studies in familial Rett syndrome Andrew R. J. CurtisSophie HeadlandShomi Bhattacharya Original Investigations Pages: 551 - 555
Exclusion of two candidate pigment loci, c and b, part of chromosome 11p, and 33 random polymorphic markers as the locus for tyrosinase-positive oculocutaneous albinism M. A. ColmanG. StevensT. Jenkins Original Investigations Pages: 556 - 560
Apolipoprotein B signal peptide polymorphism in patients with myocardial infarction and controls S. VisvikisJ. P. CambouF. Cambien Original Investigations Pages: 561 - 565
Linkage mapping of the cystathionine β-synthase (CBS) gene on human chromosome 21 using a DNA polymorphism in the 3′ untranslated region Dimitrios AvramopoulosTara CoxStylianos E. Antonarakis Original Investigations Pages: 566 - 568
A study of genetic linkage heterogeneity in 35 adult-onset polycystic kidney disease families Alan F. WrightPeter W. TeagueMichael L. Watson Original Investigations Pages: 569 - 571
Distribution of DYZ2 repetitive sequences on the human Y chromosome P. LudeñaJ. Fernández-PiquerasC. Sentís Short Communication Pages: 572 - 574
A polymorphism in the 5′ region of coagulation factor VII gene (F7) caused by an inserted decanucleotide G. MarchettiP. PatracchiniF. Bernardi OriginalPaper Pages: 575 - 576