Genetic homology and crossing over in the X and Y chromosomes of mammals Paul S. Burgoyne Review Articles Pages: 85 - 90
Identification and function of serologically detectable H-Y antigen Ulrich Müller Review Articles Pages: 91 - 94
High rate of detection of 13q14 deletion mosaicism among retinoblastoma patients (using more extensive methods) Tomiko Motegi Original Investigations Pages: 95 - 97
Incidence of chromosome abnormalities in newborn children. Comparison between incidences in 1969–1974 and 1980–1982 in the same area J. NielsenM. WohlertP. Videbech Original Investigations Pages: 98 - 101
Muscle provocation test. A sensitive method for discrimination between carriers and noncarriers of Duchenne muscular dystrophy F. H. HerrmannA. SpieglerG. Wiedemann Original Investigations Pages: 102 - 104
Cytogenetic investigations in 150 cases with complaints of sterility or primary amenorrhea Ann JosephIrene Manorama Thomas Original Investigations Pages: 105 - 109
H-Y antigen in male patients with X polysomies Wolfgang EngelBarbara KlemmeChrista Fonatsch Original Investigations Pages: 110 - 112
Macroorchidism and fragile X in mentally retarded males Karen Brøndum NielsenNiels TommerupCarsten Schou Original Investigations Pages: 113 - 117
Functional assessment of genetic variants of α1-Antitrypsin Gail D. BillingsleyDiane Wilson Cox Original Investigations Pages: 118 - 122
Three new rare variants of α1-Antitrypsin Diane Wilson CoxShirley SmythGail Billingsley Original Investigations Pages: 123 - 126
The HLA-A:HLA-B crossovers and their contribution in analysing possible haplotype-specific recombination rates K. Bender Original Investigations Pages: 127 - 134
Correlation between the number of sex chromosomes and the H-Y antigen titer M. FraccaroAntonia MayerováE. M. Ritzen Original Investigations Pages: 135 - 140
Giemsa-11 technique. Applications in the chromosomal characterization of hematologic specimens Helvise G. MorseTaru HaysArthur Robinson Original Investigations Pages: 141 - 144
Complete moles have paternal chromosomes but maternal mitochondrial DNA Douglas C. WallaceUrvashi SurtiA. E. Szulman Original Investigations Pages: 145 - 147
Gm and Km immunoglobulin allotypes in Reindeer Chukchi and Siberian Eskimos R. I. SukernikLudmila P. Osipova Original Investigations Pages: 148 - 153
Gm and Km frequencies in a Portugese population J. P. PandeyB. T. ShannonH. H. Fudenberg Original Investigations Pages: 154 - 156
Well-identifiable human chromosomes Isolated from mitotic fibroblasts by a new method Charles H. C. M. BuysTrijntje KoertsJacob A. Aten Short Communications Pages: 157 - 159
On the frequency of telomeric chromosomal changes induced by culture conditions suitable for fragile X expression P. SteinbachG. BarbiTh. Böller Short Communications Pages: 160 - 162
Cocultivation studies with cells of patients bearing fragile X chromosomes Gertrud EberleHeinrich ZanklMerve Zankl Short Communications Pages: 163 - 164
Standardization of nomenclature for transcobalamin II variants Marijke Fràter-SchröderHenk J. PorckLuca L. Cavalli-Sforza Short Communications Pages: 165 - 166
The phenotype in de novo and familial pericentric inversion 6. A problem in karyotype-phenotype correlation Angela Schmidt Clinical Case Reports Pages: 167 - 170
An excess of the Pi Sallele in dizygotic twins and their mothers P. ClarkN. G. Martin Clinical Case Reports Pages: 171 - 174
G-6-PD Guadalajara. A new mutant associated with chronic nonspherocytic hemolytic anemia G. VacaB. IbarraE. Beutler Clinical Case Reports Pages: 175 - 176
Chromosome 17 has a real fragile site at p12 F. ShabtaiD. KlarI. Halbrecht Letter to the Editors Pages: 177 - 179
