Anatomic and chromosomal anomalies in 944 induced abortuses Tadashi KajiiKoso OhamaKazuya Mikamo Original Investigations Pages: 247 - 258
Preferential X inactivation in human placenta membranes: Is the paternal X inactive in early embryonic development of female mammals? Hans-Hilger RopersGerhard WolffHelmut W. Hitzeroth Original Investigations Pages: 265 - 273
Cytogenetic examination of the NOR activity in a proband with 13/13 translocation and in her relatives H. ZanklS. Hahmann Original Investigations Pages: 275 - 279
The relation of sex, smoking status, birth rank, and parental age to β2-glycoprotein I levels and phenotypes in a sample of Australian Caucasian adults David N. Propert Original Investigations Pages: 281 - 288
Regulation of rRNA gene expression in a human familial 14p+ marker chromosome Dorothy A. MillerW. Roy BregOrlando J. Miller Original Investigations Pages: 289 - 297
The gene for human peptidase A is on band 18q23 and shows triplex and uniplex dosage effect C. DanesinoAlessandra D'AzzoM. Fraccaro Original Investigations Pages: 299 - 305
Isoelectric focusing of human red cell phosphoglucomutase S. G. WelchC. A. SwindlehurstK. Williams Original Investigations Pages: 307 - 313
Red cell glucose 6 phosphate dehydrogenase genotypes of the population of two West African villages S. G. WelchJ. LeeK. Williams Original Investigations Pages: 315 - 320
Is there a pattern of gene differentiation in the Indian populations Ranajit ChakrabortyArun K. Roychoudhury Original Investigations Pages: 321 - 328
Chromosomal investigations in children with pyknolepsy on dipropylacetate monotherapy Franz KotlarekJoachim Faust Short Communications Pages: 329 - 331
Prenatal diagnosis of Meckel syndrome Nico J. LeschotJaak J. de NefPaul F. Wiesenhaan Short Communications Pages: 333 - 336
Homozygosity of adenylate kinase allele 3: Two cases Jeanine SégerPaul TchenEtienne Bois Short Communications Pages: 337 - 339
Ring 10 chromosome: 46,XX,r10(p15q26) Robert S. SparkesShun M. LingHelga Muller Clinical Case Reports Pages: 341 - 345
Trisomy 22 in a 20-year-old female D. A. WelterL. Scharff IIIT. G. Thevaos Clinical Case Reports Pages: 347 - 351