Painting of human chromosomes with probes generated from hybrid cell lines by PCR with Alu and L1 primers C. LengauerH. RiethmanT. Cremer Original Investigations Pages: 1 - 6
Identification of functioning sweat pores and visualization of skin temperature patterns in X-linked hypohidrotic ectodermal dysplasia by whole body thermography R. P. ClarkM. R. GoffK. D. MacDermot Original Investigations Pages: 7 - 13
R-banding and nonisotopic in situ hybridization: precise localization of the human type II collagen gene (COL2A1) Ei-ichi TakahashiTada-aki HoriRay White Original Investigations Pages: 14 - 16
Rare McArdle disease locus polymorphic site on 11q13 contains CpG sequence Roger V. LeboLee A. AndersonRobert Fletterick Original Investigations Pages: 17 - 24
Selective advantage of fra (X) heterozygotes F. VogelW. E. CrusioM. Freund Original Investigations Pages: 25 - 32
Cytogenetic analysis of 400 sperm from three translocation heterozygotes Renee H. MartinLeona BarclayS. Bea Fowlow Original Investigations Pages: 33 - 39
Ha-ras-1 alleles in Norwegian lung cancer patients David RybergToril TefreAage Haugen Original Investigations Pages: 40 - 44
Detection of 98% of DMD/BMD gene deletions by polymerase chain reaction Alan H. BeggsMichel KoenigLouis M. Kunkel Original Investigations Pages: 45 - 48
Genetic heterogeneity at the glucose-6-phosphate dehydrogenase locus in southern Italy: a study on a population from the Matera district V. CalabròA. GiacobbeG. Battistuzzi Original Investigations Pages: 49 - 53
Assignment of the Nance-Horan syndrome to the distal short arm of the X chromosome D. ZhuD. M. AlcornI. H. Maumenee Original Investigations Pages: 54 - 58
A new marker at DXS 115 useful for carrier detection in hemophilia A Manfred WehnertWinnie SchröderFalko H. Herrmann Original Investigations Pages: 59 - 60
Cloning of the breakpoints of a deletion associated with choroideremia F. P. M. CremersF. BrunsmannH. H. Ropers Original Investigations Pages: 61 - 64
The human VAV proto-oncogene maps to chromosome region 19p12→19p13.2 Cecile MartinerieLinda A. CannizzaroMariano Barbacid Original Investigations Pages: 65 - 68
Haplotype distribution and molecular defects at the phenylalanine hydroxylase locus in Italy Irma DianzaniMarcella DevotoSavio L. C. Woo Original Investigations Pages: 69 - 72
The human corticosteroid binding globulin gene is located on chromosome 14q31–q32.1 near two other serine protease inhibitor genes Gilles-Eric SeraliniDominique BérubéGeoffrey L. Hammond Original Investigations Pages: 73 - 75
Neither age nor sex influence the expression of folate sensitive common fragile sites on human chromosomes Dominique F. C. M. SmeetsGerard Merkx Original Investigations Pages: 76 - 78
The Na+/H+ antiporter: a “melt” polymorphism allows regional mapping to the short arm of chromosome 1 Christopher R. K. DudleyLuis A. GiuffraStephen T. Reeders Original Investigations Pages: 79 - 83
Localization of the gene for human proliferating nuclear antigen/cyclin by in situ hybridization Graham WebbPeter ParsonsGeorgia Chenevix-Trench Short Communications Pages: 84 - 86
An HhaI polymorphism is present in factor IX genes of Asian subjects Alexander P. ReinerArthur R. Thompson Short Communications Pages: 87 - 88
Homozygosity for the met30 transthyretin gene in a Turkish kindred with familial amyloidotic polyneuropathy James SkareHasan YaziciMartha Skinner Short Communications Pages: 89 - 90
Detection by denaturing gradient gel electrophoresis of a new polymorphism in the apolipoprotein B gene Maria NavajasAnne-Marie LaurentGérard Roizès Short Communications Pages: 91 - 93
A 45,X male with molecular evidence of a translocation of Y euchromatin onto chromosome 1 Nacer AbbasGiuseppe NovelliBruno Dallapiccola Short Communications Pages: 94 - 98
Maternal transmission of ring chromosome 21 Ingo KennerknechtGotthold BarbiWalther Vogel Clinical Case Report Pages: 99 - 101
Crossover in a Spanish cystic fibrosis family Esther FernándezManuela VillamarJavier Benítez OriginalPaper Pages: 102 - 102