Application of the polymerase chain reaction to the diagnosis of human genetic disease Jochen ReissDavid N. Cooper Review Article Pages: 1 - 8
Linkage between a PvuII restriction fragment length polymorphism and G6PD A-202A/376G: evidence for a single origin of the common G6PD A — mutation Ernest BeutlerWanda Kuhl Original Investigations Pages: 9 - 11
The achondroplasia gene is not linked to the locus for neurofibromatosis 1 on chromosome 17 S.-M. PulstJ. M. Graham Jr.J. R. Korenberg Original Investigations Pages: 12 - 14
Paracentric inversion inv(11) (q21q23) in the Netherlands K. MadanM. H. E. C. PietersD. F. C. M. Smeets Original Investigations Pages: 15 - 20
Constitutional deletions predisposing to retinoblastoma Marie JansonErik KockMagnus Nordenskjöld Original Investigations Pages: 21 - 24
A deletion panel of the long arm of the X chromosome: subregional localization of 22 DNA probes H. -M. YangT. LundL. Shen Original Investigations Pages: 25 - 30
Louis-Bar syndrome: spontaneous and induced chromosomal aberrations in lymphocytes and micronuclei in lymphocytes, oral mucosa and hair root cells Rosella TomaninFranco SartoCarlo Trevisan Original Investigations Pages: 31 - 38
Assignment of the apolipoprotein A-I gene to 11q23 based on RFLP in a case with a partial deletion of chromosome 11, del(11)(q23.3→qter) Tadao ArinamiTakeki HiranoHideo Hamaguchi Original Investigations Pages: 39 - 40
On-line sorting of human chromosomes by centromeric index, and identification of sorted populations by GTG-banding and fluorescent in situ hybridization Gert A. BoschmanWim RensJacob A. Aten Original Investigations Pages: 41 - 48
Analysis of meiotic segregation in a man heterozygous for a 13;15 Robertsonian translocation and a review of the literature Franck Pellestor Original Investigations Pages: 49 - 54
The mutational spectrum of single base-pair substitutions causing human genetic disease: patterns and predictions David N. CooperMichael Krawczak Original Investigations Pages: 55 - 74
The analysis of hypervariable DNA profiles: problems associated with the objective determination of the probability of a match Peter GillKevin SullivanDavid J. Werrett Original Investigations Pages: 75 - 79
Inv(14) with distal breakpoint in 14q32.1 in three cases of T cell lymphoma Brigitte SchlegelbergerAlfred C. FellerWerner Grote Original Investigations Pages: 80 - 84
Investigation of the ZFY gene in XX true hermaphroditism and Swyer syndrome Durval DamianiAna Elisa C. BillerbeckJorge Kalil Original Investigations Pages: 85 - 88
Albumin — vitamin D-binding protein haplotypes in Asian-Pacific populations Liang Zhong ChenSimon EastealRobert L. Kirk Original Investigations Pages: 89 - 97
Identification of a hypervariable microsatellite polymorphism within D9S15 tightly linked to Friedreich's ataxia Julie WallisRobert WilliamsonSusan Chamberlain Original Investigations Pages: 98 - 100
Loss of heterozygosity of the L-myc oncogene in human breast tumors Ivan BiecheMarie-Helene ChampemeRosette Lidereau Original Investigations Pages: 101 - 105
Fetal hemoglobin in normal adults and β-thalassemia heterozygotes Abdullah KutlarFerdane KutlarTitus H. J. Huisman Original Investigations Pages: 106 - 110
Molecular analyses of a Lesch-Nyhan syndrome mutation (hprt Montreal) by use of T-lymphocyte cultures Thomas R. SkopekLeslie RecioRichard J. Albertini Original Investigations Pages: 111 - 116
DXS26 (HU16) is located in Xq21.1 Eeva-Marja SankilaGail A. P. BrunsAlbert de la Chapelle Short Communications Pages: 117 - 120
RFLP-patterns in Japanese PKU families: new polymorphisms for the mutant phenylalanine hydroxylase gene Friedrich K. TrefzM. YoshinoDavid S. Konecki Short Communications Pages: 121 - 122
Detection of point mutation in the tyrosinase gene of a Japanese albino patient by a direct sequencing of amplified DNA Hideaki KikuchiSatoshi HaraMinro Watanabe Short Communications Pages: 123 - 124
Regional localization by in situ hybridization of a human chromosome 9 marker tightly linked to the Friedreich's ataxia locus Elena RaimondiAntonella AntonelliMassimo Pandolfo Short Communications Pages: 125 - 126
Direct estimation of serological H-Y antigen by flow cytometry Marijo KentStephen WachtelH. Tzvi Thaler Short Communications Pages: 127 - 129
Regional chromosomal assignment of the human mineralocorticoid receptor gene to 4q31.1 Norma MorrisonStephen B. HarrapJ. Michael Connor Short Communications Pages: 130 - 132
Failure to document fetal cells in maternal circulation using the Selypes-Lorencz “air-culture” cytogenetic technique Mounira YoussefLee P. ShulmanSherman Elias Short Communications Pages: 133 - 134
Mediterranean types of β-thalassemia in the German population Marion LaigMichael PapeGebhard Flatz Short Communications Pages: 135 - 137
A case of ring chromosome 15 accompanied by almost normal intelligence Mashio KitataniHiroaki TakahashiTatsuya Maruoka Clinical Case Report Pages: 138 - 139
An informative MspI polymorphism detected at the D21S16 locus G. Van CampA. VandenbergheC. Van Broeckhoven OriginalPaper Pages: 140 - 140
Recombination and the fragile X Graeme K. SuthersGrant R. Sutherland Letters to the Editors Pages: 141 - 142
Unusual segregation of constitutional 11q;22q translocation may be explained by crossover in interchange segment, followed by 3∶1 segregation at meiosis I R. H. Lindenbaum Letters to the Editors Pages: 143 - 143
