Langer-Giedion syndrome with and without del 8q. Assignment of critical segment to 8q23 Catherine TurleauFrançoise Chavin-ColinH. Rivera Original Investigations Pages: 183 - 187
Glycoproteins that distinguish different cell types found in amniotic fluid Ann Harris Original Investigations Pages: 188 - 192
Transmission of the PiZ allele for α1-antitrypsin deficiency: Population genetic considerations R. ChakrabortyJ. ConstansP. P. Majumder Original Investigations Pages: 193 - 197
Clastogenic effect of the psychotropic drug thioridazine on human chromosomes in vivo R. SaxenaY. R. Ahuja Original Investigations Pages: 198 - 200
Analysis of chromosome positions in the interphase nucleus of Chinese hamster cells by laser-UV-microirradiation experiments T. CremerC. CremerM. Kirsch-Volders Original Investigations Pages: 201 - 209
Pericentric X inversion in dizygotic twins who differ in X chromosome inactivation and menstrual cycle function Elisabeth A. KeitgesCatherine G. PalmerDavid D. Weaver Original Investigations Pages: 210 - 213
Analysis of linkage relationships in maturity-onset diabetes of young people and independent segregation of C6 and HLA S. W. SerjeantsonP. Zimmet Original Investigations Pages: 214 - 216
Polymorphism of human chromosomes 1, 9, 16, Y: Variations, segregation and mosaicism Silvana SimiF. Tursi Original Investigations Pages: 217 - 220
Fetal cells in the maternal circulation: Detection by direct AFP-immunofluorescence Andreas KulozikIvar Harry Pawlowitzki Original Investigations Pages: 221 - 224
Male infertility in a case of (Y;6) balanced reciprocal translocation. Mitotic and meiotic study F. ViguiéF. RomaniJ. P. Dadoune Original Investigations Pages: 225 - 227
Endomitosis in human trophoblast Gloria E. SartoPatricia A. StubblefieldEeva Therman Original Investigations Pages: 228 - 232
The locus for apolipoprotein E (apoE) is linked to the complement component C3 (C3) locus on chromosome 19 in man B. OlaisenP. TeisbergT. Gedde-Dahl Jr. Original Investigations Pages: 233 - 236
RHG-band polymorphism of the short arms of human acrocentric chromosomes and relationship of variants to satellite associations P. BalíčekJ. ŽižkaH. Skalská Original Investigations Pages: 237 - 239
The Meckel syndrome. Pathological and cytogenetic observations in eight cases Ph. MoermanE. VerbekenJ. M. Lauweryns Original Investigations Pages: 240 - 245
A rare phenotype of phosphoglucomutase-2 first detected in Mongoloids I. NishigakiT. ItohI. Hasegawa Original Investigations Pages: 246 - 249
Genetic hemoglobin abnormalities in 2363 Cuban newborns G. MartínezM. E. Cañizares Original Investigations Pages: 250 - 251
Human chromosomal polymorphism. III. Chromosomal Q polymorphism in Mongoloids of northern Asia A. I. IbraimovM. M. Mirrakhimov Original Investigations Pages: 252 - 257
Human chromosomal polymorphism. IV. Chromosomal Q polymorphism in Russians living in Kirghizia A. I. IbraimovM. M. Mirrakhimov Original Investigations Pages: 258 - 260
Human chromosomal polymorphism. V. Chromosomal Q polymorphism in African populations A. I. IbraimovM. M. Mirrakhimov Original Investigations Pages: 261 - 265
Data and theory for a revised chiasma map of man Newton E. MortonJan LindstenShirley Yee Original Investigations Pages: 266 - 270
Translocation(X;Y)(p22.33;p11.2) in XX males: Etiology of male phenotype R. E. MagenisM. J. WebbE. Lovrien Original Investigations Pages: 271 - 276
Meiotic chromosomes in a female with primary trisomic Down's syndrome Paul PolaniJohn Sir DewhurstJennifer Kelberman Short Communications Pages: 277 - 279
Gene mapping and serendipity. The locus for torticollis, keloids, cryptorchidism and renal dysplasia (31430, McKusick) is at Xq28, distal to the G6PD locus Orsetta ZuffardiM. Fraccaro Short Communications Pages: 280 - 281
Replication status of the fragile X chromosome, fra(X)(q27), in three heterozygous females R. T. HowellA. McDermott Short Communications Pages: 282 - 284
Prenatal detection of a fetus hemizygous for the fragile X-chromosome Angela SchmidtE. PassargeM. Macek Short Communications Pages: 285 - 286
Determination of the H-Y antigen in amniotic cells. Its use in prenatal diagnosis B. Rafael ElejaldeMaria Mercedes de Elejalde Clinical Case Reports Pages: 287 - 288
Repeated anencephaly and XO/XX mosaicism in the mother Tahseen FatimaTangirala MalatiT. Seetha Cases Observed Pages: 289 - 289
