Detection of a common mutation of the catalase gene in Japanese acatalasemic patients Yosuke KishimotoYoshinori MurakamiTakao Sekiya Original Investigations 01 March 1992 Pages: 487 - 490
Complementation study of peroxisome-deficient disorders by immunofluorescence staining and characterization of fused cells Shigehiro YajimaYasuyuki SuzukiHugo W. Moser Original Investigations 01 March 1992 Pages: 491 - 499
Genetic concepts in Greek literature from the eighth to the fourth century B.C. Euterpe Bazopoulou-Kyrkanidou Original Investigations 01 March 1992 Pages: 500 - 507
CFTR illegitimate transcription in lymphoid cells: quantification and applications to the investigation of pathological transcripts Nuria FonknechtenJamel ChellyJean-Claude Chomel Original Investigations 01 March 1992 Pages: 508 - 512
Quantitative correlation between the residual activity of β-hexosaminidase A and arylsulfatase A and the severity of the resulting lysosomal storage disease P. LeinekugelS. MichelK. Sandhoff Original Investigations 01 March 1992 Pages: 513 - 523
Complementation of a DNA repair deficiency in six human tumor cell lines by chromosome 11 R. ParshadF. M. PriceK. K. Sanford Original Investigations 01 March 1992 Pages: 524 - 528
Molecular genetic evidence for a founder effect in familial hypercholesterolemia among French Canadians Christine BétardA. M. KesslingJ. Davignon Original Investigations 01 March 1992 Pages: 529 - 536
Nested polymerase chain reaction on cellular DNA in plasma: a rapid method to investigate the collagen type I A2 MspI polymorphic restriction site in alcoholic patients Laurence ChristaJean-Pierre ZarskiChristian Bréchot Original Investigations 01 March 1992 Pages: 537 - 540
In situ hybridization of PCR amplified inter-Alu sequences from a hybrid cell line C. DesmazeJ. ZucmanA. Aurias Original Investigations 01 March 1992 Pages: 541 - 544
CYP21/C4 gene organisation in Italian 21-hydroxylase deficiency families Paul J. SinnottChiara LivieriTom Strachan Original Investigations 01 March 1992 Pages: 545 - 551
Screening for cystic fibrosis gene mutations by multiplex DNA amplification Luigi PicciFranca AnglaniFranco Zacchello Original Investigations 01 March 1992 Pages: 552 - 556
Polymorphisms at the GLUT1 (HepG2) and GLUT4 (muscle/adipocyte) glucose transporter genes and non-insulin-dependent diabetes mellitus (NIDDM) Marco G. BaroniRaymond S. OelbaumDavid J. Galton Original Investigations 01 March 1992 Pages: 557 - 561
Genetic linkage analysis of bipolar affective disorder in an Old Order Amish pedigree Adam LawCharles W. Richard IIIRichard M. Myers Original Investigations 01 March 1992 Pages: 562 - 568
The human vitronectin (complement S-protein) gene maps to the centromeric region of 17q Thomas M. FinkDieter E. JennePeter Lichter Original Investigations 01 March 1992 Pages: 569 - 572
Pseudoautosomal repeat displays higher variability in Blacks than in Caucasians Gudrun A. RappoldAnja HenkeTitus H. J. Huisman Original Investigations 01 March 1992 Pages: 573 - 578
Search for putative suppressor genes in meningioma: significance of chromosome 22 Günther SchneiderSteffi LutzNikolaus Blin Original Investigations 01 March 1992 Pages: 579 - 582
PCR-assisted localization of the human SRPR gene Nicolas JaninOliver DelattreMarc Lipinski Short Communications 01 March 1992 Pages: 583 - 585
Protein C deficiency and thromboembolism: recurrent mutation at Arg 306 in the protein C gene C. B. GrundyS. SchulmanD. N. Cooper Short Communications 01 March 1992 Pages: 586 - 588
Characterization of two novel polymorphisms at the human parathyroid hormone gene locus Jerald E. MullersmanJack J. ShieldsBratin K. Saha Short Communications 01 March 1992 Pages: 589 - 592
Localization of the human gene encoding heterogeneous nuclear RNA ribonucleoprotein G (hnRNP-G) to chromosome 6p12 Maryvonne Le ConiatMichel SoulardRoland Berger Short Communications 01 March 1992 Pages: 593 - 595
De novo complex chromosome rearrangement in identical twins with multiple congenital anomalies Yoshiharu WakitaKouji NaraharaYoshiki Seino Clinical Case Report 01 March 1992 Pages: 596 - 598
Selective advantage of fra(X) heterozygotes compared with mothers of Down syndrome probands? P. H. Jongbloet Letters to the Editors 01 March 1992 Pages: 599 - 600
Mothers and grandmothers of Down's syndrome patients as controls for fra(X) carriers F. Vogel Letters to the Editors 01 March 1992 Pages: 601 - 601