A familial paracentric inversion: A short review of the current status Philippus A. VenterBronwin DawsonJohann Op't Hof Original Investigations Pages: 121 - 125
Reproductive outcomes of paracentric inversion carriers: Report of a liveborn dicentric recombinant and literature review E. H. MulesJ. Stamberg Original Investigations Pages: 126 - 131
Coagulation factor XIII: A useful polymorphic genetic marker J. B. GrahamC. J. S. EdgellR. C. Elston Original Investigations Pages: 132 - 135
DNA polymerase α inhibition by aphidicolin induces gaps and breaks at common fragile sites in human chromosomes Thomas W. GloverCarol BergerBarbara Echo Original Investigations Pages: 136 - 142
A nonparametric and a parametric version of a test for the detection of the presence of a major gene applicable on data for the complete nuclear family Suresh D. JayakarJohn A. WilliamsonLaura Zonta-Sgaramella Original Investigations Pages: 143 - 150
Familial apolipoprotein CII deficiency: A preliminary analysis of the gene defect in two independent families S. E. HumphriesL. WilliamsR. Williamson Original Investigations Pages: 151 - 155
Unbalanced reciprocal translocations in cases of Prader-Willi syndrome David P. DuckettSelwyn H. RobertsPatricia Davies Original Investigations Pages: 156 - 161
Meiotic studies and synaptonemal complex analysis in two infertile males with a 13/14 balanced translocation C. TempladoF. VidalJ. Egozcue Original Investigations Pages: 162 - 165
Population and formal genetics of the human C81(α-γ) polymorphism Christian RittnerWaltraud HargesheimerEva Mollenhauer Original Investigations Pages: 166 - 169
Atypical metachromatic leukodystrophy? T. TønnesenC. VrangH. O. Lou Original Investigations Pages: 170 - 173
The beta chorionic gonadotropin-beta luteinizing gene cluster maps to human chromosome 19 C. JulierD. WeilC. Junien Original Investigations Pages: 174 - 177
The locus for apolipoprotein E (apoE) is close to the Lutheran (Lu) blood group locus on chromosome 19 T. Gedde-Dahl JrB. OlaisenR. Helland Original Investigations Pages: 178 - 182
Estimating the Recombination frequency for the PTC-Kell linkage M. Anne-SpenceCatherine T. FalkRobert S. Sparkes Original Investigations Pages: 183 - 186
A de novo case of trisomy 10p: Gene dosage studies of hexokinase, inorganic pyrophosphatase and adenosine kinase F. F. SnyderC. C. LinJ. J. Hoo Original Investigations Pages: 187 - 189
Harvey-ras allele deletion detected by in situ hybridization to Wilms' tumor chromosomes Michael R. EcclesLynn J. MillowAnthony E. Reeve Original Investigations Pages: 190 - 192
New chromosomal syndrome: Miller-Dieker syndrome and monosomy 17p13 Robert F. StrattonWilliam B. DobynsDavid H. Ledbetter Original Investigations Pages: 193 - 200
Facioscapulohumeral muscular dystrophy concentrated in the village Çullar, Nevşhir, Turkey Bekir Sitki ŞayliKorkut YaltkayaŞükrü Cin Original Investigations Pages: 201 - 208
PI (α1) polymorphism in the Japanese: Confirmation of PI*M4 and description of new PI variants I. YuasaK. SuenagaK. Okada Original Investigations Pages: 209 - 212
Comparison of expression of the fragile site at Xq27 in T and B lymphocytes Cristiana A. MarcheseMing S. LinMiriam G. Wilson Short Communications Pages: 213 - 213
The Cd technique identifies a specific structure related to centromeric function Simonetta LambiasePaola MaraschioOrsetta Zuffardi Short Communications Pages: 214 - 215
A leftward deletional α+ thalassemia found in East Sicily in conjunction with heterozygous β-thalassemia Constantin TroungosRajagopal KrishnamoorthyDominique Labie Short Communications Pages: 216 - 218
Trisomy 11p15 and Beckwith-Wiedemann syndrome. A report of two cases Catherine TurleauJean de GrouchyRobert Charlas Clinical Case Reports Pages: 219 - 221
Prenatal identification of a deleted Y chromosome by cytogenetics and a Y-specific repetitive DNA probe C. DistecheD. LuthyD. Hoar Clinical Case Reports Pages: 222 - 224
Analysis of the DNA replication pattern of a translocation (tX/X, qter→p221::p223→qter) chromosome in leukocyte and fibroblast cultures F. PellicciaM. FerraroA. de Capoa Clinical Case Reports Pages: 225 - 229
Is a gene for microcephaly located on chromosome 1? Amalia Pérez-CastilloMaría Angeles Martín-LucasJ. A. Abrisqueta Clinical Case Reports Pages: 230 - 232
Identical twins with deletion 16q syndrome: Evidence that 16q12.2-q13 is the critical band region F. F. B. ElderJ. W. FergusonL. H. Lockhart Cases Observed Pages: 233 - 236
Interstitial deletion of the short arm of chromosome 17 S. R. PatilJ. A. Bartley Cases Observed Pages: 237 - 238
Meiotic translocations in two sterile males C. TempladoJ. NavarroJ. Egozcue Cases Observed Pages: 239 - 239