Gene organization of haplotypes expressing two different C4A allotypes A. PalsdottirA. ArnasonO. Jensson Original Investigations Pages: 220 - 224
Submicroscopic duplication of chromosome 21 and trisomy 21 phenotype (Down syndrome) J. M. DelabarP. M. SinetJ. de Grouchy Original Investigations Pages: 225 - 229
Sporadic cases in Duchenne muscular dystrophy Antonella RussoGuido BarbuianiGian Antonio Danieli Original Investigations Pages: 230 - 235
Human δ-aminolevulinate dehydratase: chromosomal localization to 9q34 by in situ hybridization Venkateswara R. PotluriKenneth H. AstrinRobert J. Desnick Original Investigations Pages: 236 - 239
An improved method for detecting Y chromosomal DNA John R. D. StalveyRobert P. Erickson Original Investigations Pages: 240 - 243
Isoacentric and isocentric chromosomes originating after deletions of human chromosomes B. DutrillauxW. Al AchkarE. Viegas-Pequignot Original Investigations Pages: 244 - 247
Linkage analysis with RFLPs in families with androgen resistance syndromes: evidence for close linkage between the androgen receptor locus and the DXS1 segment Peter WieackerJames E. GriffinMeinert Breckwoldt Original Investigations Pages: 248 - 252
RFLP analysis in families with sporadic hemophilia A F. BernardiG. MarchettiF. Conconi Original Investigations Pages: 253 - 256
Detection of submicroscopic deletions and a DNA polymorphism at the retinoblastoma locus B. HorsthemkeValerie GregerE. Passarge Original Investigations Pages: 257 - 261
MspI polymorphic site within the Factor IX gene Debra L. FreedenbergShi-Han ChenC. Ronald Scott Original Investigations Pages: 262 - 264
Contribution of magnetic resonance imaging to the knowledge of CNS malformations related to chromosomal aberrations J. C. TamrazMarie-Odile RethoréE. A. Cabanis Original Investigations Pages: 265 - 273
Rapid RFLP screening procedure identifies new polymorphisms at albumin and alcohol dehydrogenase loci Jeffrey C. MurrayRita ShiangKenneth H. Buetow Original Investigations Pages: 274 - 277
Biochemical and genetic exclusion of calmodulin as the site of the basic defect in cystic fibrosis P. J. ScamblerM. A. McPhersonR. Williamson Original Investigations Pages: 278 - 282
Assignment of the human gamma-glutamyl transferase gene to the long arm of chromosome 22 F. BulleM. G. MatteiG. Guellaën Original Investigations Pages: 283 - 286
Human α-globin maps to pter-p13.3 in chromosome 16 distal to PGP M. H. BreuningK. MadanP. L. Pearson Original Investigations Pages: 287 - 289
A method for nucleic acid hybridization to isolated chromosomes in suspension Gertrud DudinThomas CremerChristoph Cremer Original Investigations Pages: 290 - 292
Detection of BrdUrd incorporation in mammalian chromosomes by a BrdUrd antibody A. Latos-BielenskaH. HameisterW. Vogel Short Communications Pages: 293 - 295
Different severity of homozygous β-thalassemia among siblings P. WinichagoonS. FucharoenP. Wasi Short Communications Pages: 296 - 297
Trisomy 22 in a newborn with multiple malformations I. VoiculescuElke BackW. Schempp Clinical Case Report Pages: 298 - 301
Ring chromosome 15 in a mother and her children Wakae FujimakiKeiko BabaYasushige Mashima Case Observed Pages: 302 - 302